Ability to understand and the willingness to sign a written informed consent document or a parent/guardian able to do the same
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to read, understand and evaluate study materials and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and if a minor, have a guardian who meets the above criteria
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; informed consent must be provided prior to any study specific procedures
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Must have an ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand, and the willingness to sign, a written informed consent document, as well as comply with study requirements
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Must possess the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
The patient if 18 years or more or a minor’s guardian must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent and HIPAA consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
PHASE II INCLUSION CRITERIA: Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
ENROLLMENT TO THE DOSE ESCALATION, EXPANSION AND PART II: Ability to understand and the willingness to sign a written informed consent document
EXPANDED ACCESS COHORT: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand the willingness and to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it; assent will be obtained when appropriate based on the subjects age
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Participants must have the ability to understand, and the willingness to sign, a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of the research subject or authorized legal representative to understand and have the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patient and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
Ability of subject to understand, adhere to protocol requirements and the willingness to sign a written informed consent document
Written informed consent must be obtained from all patients prior to beginning therapy; patients should have the ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of a subject to understand and the willingness to sign the informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and to undergo tumor biopsies in the expansion phase
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent and HIPAA consent document.
Ability to understand and the willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document.
Participants and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
STRATUM A: Participants and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
STRATUM B: Participants and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
STRATUM C: Participants and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign a written informed consent document
Written informed consent must be obtained from all patients prior to beginning therapy; patients should have the ability to understand and the willingness to sign a written informed consent document
Patients must be able to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it. Assent will be obtained when appropriate based on the subjects age.
Ability to understand and willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
COHORT 1: HORMONE RECEPTOR POSITIVE BREAST CANCER: Ability of subject to understand and the willingness to sign a written informed consent document
COHORT 2: TRIPLE NEGATIVE BREAST CANCER: Ability of subject to understand and the willingness to sign a written informed consent document
COHORT 3: ENDOMETRIAL CANCER: Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document prior to initiation of any screening or study-specific procedures
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
Ability to understand and willingness to sign a written informed consent document (I-SPY 2 TRIAL Consent #2)
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; only subjects who have capacity to consent will be enrolled in the study
Ability to understand and the willingness to sign a written informed consent document; written informed consent must be obtained prior to any screening procedures
Subjects must have the ability to understand and the willingness to sign a written informed consent document.
Subjects must have the ability to understand and the willingness to sign a written informed consent document.
Ability to understand and willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Has the ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability of subject or legally guardians (if the patient is < 18 years old) to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand English and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
PHASE I: Subjects must have the ability to understand and the willingness to sign a written informed consent document
PHASE II: Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability and willingness to sign a written informed consent document
Must be informed of the investigational nature of this study and must have the ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
DONOR: Ability to understand and willingness to sign an IRB approved written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
No study specific procedures will be performed without a written and signed informed consent document; patients who do not demonstrate the ability to understand or the willingness to sign the written informed consent document will be excluded from study entry
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Consent: patients must have the ability to understand and the willingness to sign a written informed consent or assent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign written informed consent document(s)
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
PHASE II: Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document.
Ability of subject to understand and the willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of participant to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
DONOR: Ability to understand and willingness to sign an IRB approved written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Written informed consent must be obtained from all patients prior to study registration; patients should have the ability to understand and the willingness to sign a written informed consent document
UROTHELIAL CARCINOMA EXPANSION COHORT: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of patient to understand and the willingness to sign a written informed consent document prior to any protocol related procedures, including screening evaluations.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign written informed consent document(s)
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must demonstrate an ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
CAPMATINIB INCLUSION CRITERIA: Ability to understand a written informed consent document, and the willingness to sign it
CERITINIB INCLUSION CRITERIA: Ability to understand a written informed consent document, and the willingness to sign it
REGORAFENIB INCLUSION CRITERIA: Ability to understand a written informed consent document, and the willingness to sign it
ENTRECTINIB INCLUSION CRITERIA: Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
All patients must be informed of the investigational nature of this study and must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of participant (or parent/guardian for participants who are minors) to understand and the willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written Informed Consent and HIPAA document/s
Ability of subject to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign an IRB approved written informed consent document.
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; patients must have signed informed consent to participate in the trial
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Informed consent - no study specific procedures will be performed without a written and signed informed consent document; patients who do not demonstrate the ability to understand or the willingness to sign the written informed consent document will be excluded from study entry
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
PART 1: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and consent to the serial nature of the proposed Personalized ANtibodies for Gastro-Esophageal Adenocarcinoma (PANGEA) treatment with first, second and third line therapy as tolerated
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign the informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability of the patient or the patient’s legal guardian to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign the informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Participants must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document for both screening and treatment; signed informed consent must be obtained prior to screening or treatment
ELIGIBILITY CRITERIA FOR REGISTRATION: ability to understand and the willingness to sign a written informed consent document
The ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
The ability to understand and the willingness to sign a written informed consent document are necessary
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document are required
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand & willingness to sign a written informed consent document.
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
1. Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document;
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign/date a written informed consent document
PRE REGISTRATION – INCLUSION CRITERIA: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of parent or guardian to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
TUMOR BIOPSY SEQUENCING: Ability to understand and the willingness to sign a written informed consent document (subjects with impaired decision-making capacity are not eligible)
Ability to understand and the willingness to sign a written informed consent document
Patients must be able to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Able to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of parent or guardian to understand and the willingness to sign a written informed consent document
DONORS will have the ability to understand and the willingness to sign a written informed consent document for bone marrow harvest.
PSTAT3 SCREENING: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to provide a written informed consent\n             document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Written informed consent must be obtained from all patients prior to beginning therapy; patients should have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of patient to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability and willingness to sign a written informed consent document
Subjects should have the ability to understand and the willingness to give verbal and sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document for the search phase
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
No study specific procedures will be performed without a written and signed informed consent document; patients who do not demonstrate the ability to understand or the willingness to sign the written informed consent document will be excluded from study entry
Ability to understand and willingness to sign a written informed consent document
Ability to understand a written informed and consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document according to institutional guidelines.
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent/assent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document prior to any study specific procedures, sampling, and analyses
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document before performance of any study related procedure not part of standard medical care
Ability to understand a written informed consent document, and the willingness to sign and date it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Written informed consent must be obtained from all patients prior to beginning therapy; patients should have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; signed informed consent will be obtained prior to any screening procedures
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand the study regimen and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign an informed consent document
PHASE I: Ability to understand and the willingness to sign a written informed consent document
PHASE II: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; consent will be obtained by day 14 of AcDVP-16 induction regimen
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
The patient or his/her legal representative must have the ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and sign an informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
PART B: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of participant (or parent/guardian for participants who are minors) to understand and the willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document (all cohorts)
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of the patient or the patient’s legal guardian to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document. Pediatric patients must sign an assent with a parent or legal guardian sign a written informed consent. Inclusion Criteria:
Ability to understand and the willingness to sign a written informed consent document. Pediatric patients must sign an assent with a parent or legal guardian sign a written informed consent.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Participant must have the ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must demonstrate ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Patients must have an ability to understand and willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Patients must have the ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document.
Ability to comply with intravenous administration schedule, and the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document in English
Subject has the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign an IRB approved written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed Consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and sign an informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
The participant has the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document or have a surrogate with the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to provide written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Be able to understand a written informed consent document and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document, or assent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Be able to understand and have willingness to sign a written informed consent document
Ability to understand and the willingness to sign and informed consent document in English
Patients must be able to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients must have the ability to understand and the willingness to sign a written informed consent document
PARENT OR GUARDIAN: Ability to understand and willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document, including the willingness to accept risk of unrelated donor stool
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Patients, or legal representative, must have the ability to understand and the willingness to sign a written informed consent document
Patients will be included only if they have the ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and to answer a questionnaire
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign an approved written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and medical release form
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and medical release
The ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and medical release
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
All subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
No study specific procedures will be performed without a written and signed informed consent document; patients who do not demonstrate the ability to understand or the willingness to sign the written informed consent document will be excluded from study entry
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to provide informed consent and sign a written informed consent document (ICD)
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and medical release
Ability to understand and the willingness to sign a written informed consent document in English or Spanish or Hebrew
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand, and the willingness to sign, a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to under and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document by the legal representative(s) of the participant
Ability to understand and the willingness to sign a written assent document by the participant
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document in English
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document; subjects must be willing to adhere to dose and visit schedules
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document and follow study procedures
Participants must have the ability to understand, and the willingness to sign, a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to provide informed consent and sign a written informed consent document (ICD)
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document and the willingness to sign it
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to provide informed consent and sign a written informed consent document (ICD)
2. Ability to understand and willingness to sign Informed Consent Document (ICD)
ALL PARTICIPANTS: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document (ICD)
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document, or have a representative able to consent for the subject
Ability to understand and the willingness to sign a written informed consent document
Participant must have ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Group I: Ability to understand and the willingness to sign a written informed consent document
Group II: Ability to understand and the willingness to sign a written informed consent document
Group III: Ability to understand and the willingness to sign a written informed consent document
OVARIAN CANCER PARTICIPANTS: Ability to understand and the willingness to sign a written informed consent document
BREAST CANCER PARTICIPANTS: Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
HEALTHY VOLUNTEERS: Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Subjects must have the ability to understand and willingness to sign a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document prior to any study specific procedures, sampling, and analyses
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Patient must have the ability to understand and the willingness to sign a written informed consent document or have a parent or guardian with the ability to understand and the willingness to sign the written informed consent
Patients must have the ability to understand and willingness to sign a written informed consent document
Ability to understand the study protocol, participate in testing, and the willingness to sign a written informed consent document
Ability to understand a written informed consent document and the willingness to sign it
Women must have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand a written informed consent document, and the willingness to sign it
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document indicating their willingness to have their tissue or biologic fluid specimens used for research as outlined in this protocol
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign a written informed consent document
Patients must have the ability to understand and willingness to sign a written informed consent document
Ability of subject to understand and the willingness to sign a written informed consent document
The participant has the ability to understand, and the willingness to sign, a written informed consent document.
The participant has the ability to understand, and the willingness to sign, a written informed consent document.
Ability to understand and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document
Subjects will have the ability to understand, and the willingness to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document and comply with all procedures
Ability to understand a written informed consent document
Ability to understand and the willingness to provide written informed consent to participate
Subject has the ability to understand and provide signed informed consent
Male or female, ? 18 years old with the ability to understand and provide signed and witnessed informed consent, and agree to comply with protocol requirements
Ability to understand the nature of this study and give written informed consent.
Ability to provide and understand written informed consent prior to any study procedures
Ability to understand and willing to provide informed consent
Ability to understand the nature of this trial and give written informed consent.
Ability to understand and willingness to provide informed consent
Ability to understand and willingness to provide informed consent.
Ability to understand and provide signed informed consent
Ability to understand and provide informed consent
Ability to understand and provide informed consent
Patient has the ability to understand and provide signed informed consent
Ability to understand and the willingness to provide informed consent
Ability to understand and provide informed consent
Ability to understand and provide informed consent
INCLUSION CRITERIA FOR PATIENTS WITH NSCLC OR TNBC (COHORT B): Ability to understand and provide informed consent
INCLUSION CRITERIA FOR TNBC: Ability to understand and provide informed consent
Ability to understand and provide signed informed consent
Patient must have the ability to understand the requirements of the study and provide informed consent.
Patient has the ability to understand and provide signed informed consent
Ability to understand and provide signed informed consent
Ability to understand and the willingness to provide written informed consent
Ability to understand and the willingness to sign a written informed consent document, and willing to provide blood samples before and during preoperative therapy; patients are also asked but not required to have research biopsies performed before and after therapy
Ability to understand and provide signed informed consent that fulfills Institutional Review Board’s guidelines
Ability to understand and provide informed consent
Ability to understand and willingness to give informed consent
Ability to understand the requirements of the study, provide written informed consent.
Ability to provide written informed consent and to understand and comply with the requirements of the study
Ability to understand and willingness to provide informed consent.
Ability to understand a written informed consent
Ability to understand and provide voluntary written informed consent
Ability to understand and willingness to provide informed consent, and the willingness to comply with the requirements of the protocol; informed consent may be obtained with the assistance of a medical translator according to institutional policies
Ability to understand and the willingness to provide written informed consent
Ability to understand and the willingness to provide informed consent
Ability to understand and provide written informed consent
Ability to provide and understand written informed consent prior to any study procedures
Ability to understand and the willingness to provide written informed assent or consent
Ability to understand the nature of this study and give written informed consent.
Patients must have the ability to understand and the willingness to provide signed written informed consent document
Ability to understand and the willingness to provide informed consent
Ability to understand the investigational nature of this study and to give informed consent
Ability to understand informed consent and signing of written informed consent document prior to initiation of protocol therapy
Ability to understand and provide informed consent
DONOR: Ability to understand and provide informed consent for all study procedures including partial liver transplant and bone marrow harvest
DONOR: Ability to understand and provide informed consent for all study procedures including liver transplant and bone marrow harvest
Ability to understand the nature of this study and give written informed consent.
Ability to understand the nature of this trial and give written informed consent
Must have the ability to understand and the willingness to provide a written informed consent to participate in the study
Ability to read, understand and provide written consent to participate in the study
Ability to understand and provide informed consent
DONOR: Ability to understand and provide informed consent for all study procedures including kidney transplant and bone marrow harvest
Patients with the ability to understand and give written informed consent for participation in this trial, including all evaluations and procedures as specified by this protocol.
Patients with the ability to understand and give written informed consent for participation in this trial, including all evaluations and procedures as specified by this protocol.
Ability to understand and the willingness to provide informed consent to participate
Ability to understand and complete written informed consent
Ability to understand and provide written informed consent to participate in this study.
This protocol is eligible for waiver of informed consent documentation; all subjects must have the ability to understand and the willingness to provide verbal informed consent
This protocol is eligible for waiver of informed consent documentation; all subjects must have the ability to understand and the willingness to provide verbal informed consent
All subjects must have the ability to understand and the willingness to participate in the informed consent process, although a waiver of written informed consent is obtained for this study
Ability to understand and the willingness to provide written informed consent
All participants must have the ability to understand the willingness to provide informed consent
All subjects must have the ability to understand and the willingness to participate in the informed consent process
This protocol is eligible for waiver of informed consent documentation; all subjects must have the ability to understand and the willingness to provide verbal informed consent
Ability to sign informed consent and understand the nature of a placebo-controlled trial
Ability to understand and the willingness to provide informed consent.
Ability to understand and give informed consent
Ability to understand and willingness to provide informed consent
Ability to understand and the willingness to provide informed consent
Ability to understand informed consent and signing of written informed consent prior to initiation of protocol therapy
Ability to understand the investigational nature of the study and provide informed consent
Have the ability to understand and to give written informed consent as assessed by the participant’s primary care physician or medical oncologist
Patient has the ability to understand and provide signed informed consent.
Ability to understand the nature of this trial and give written informed consent.
Willingness and ability to consent (and assent if under age 18) for self to participate in study
Patients (at National Cancer Institute [NCI] Community Oncology Research Program [NCORP] Institutions only) must be offered the opportunity to participate in the S1207-E01 Behavioral and Health Outcomes study (BAHO); NOTE: patients who have already started endocrine therapy are eligible for the BAHO study
Patients must be offered the opportunity to participate in specimen banking
Patients must be offered the opportunity to participate in specimen banking
Patients must not plan to participate in any other clinical trials while receiving treatment on this study or being followed post-protocol therapy
Willingness and ability to consent to participate in study
A female is eligible to enter and participate in this study if the following apply:
Has any other reason(s) for the investigator to consider that the subject should not participate in the study.
Willing to agree that the local medical oncologist may be informed that patient has agreed to participate in the study
Patients must be geographically accessible and willing to participate in all stages of treatment
All patients have to agree to participate in the correlative study of sample collection for immune correlative assays in order to participate in the main study; however, if the sample cannot be obtained due to feasibility issues, the patient will be allowed to continue on treatment
Patients who are on active surveillance for untreated localized disease may not participate in this study
Participant is willing and able to participate for the duration of the study
Participates or intends to participate in another drug study (other than observational studies) during the study
Clinical judgment by the investigator that the patient should not participate in the study
Patients from outside of the United States may participate in the study
Patients unable to read/write in English are eligible to participate in the overall study but will not participate in the patient-reported outcome questionnaires throughout the trial.
Subjects willing to participate in the study for at least 8 months
Willingness and ability to consent for self to participate in study
Must have voluntarily agreed to participate and have signed the informed consent, and are willing to complete all study procedures.
Clinical judgment by the investigator that the patient should not participate in the study
Patients must give documented informed consent to participate in this study
Patient refusal to participate in randomization
Has given written consent to participate in the study.
Agree to participate in biopsy of metastatic lesion during the study at day 21
Willingness and ability to consent for self to participate in study
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must agree to participate and be able to understand and provide informed consent to participate in the trial
Must consent to participate in study I 03103: Roswell Park Cancer Institute (RPCI) Data Bank and Biorepository (DBBR)
Subject must be capable and reliable to participate in all study related procedures
Patients must be willing to participate in all stages of treatment
Patients in the expansion cohort must also agree to participate in the biomarker study. However, patients in the Melanoma KIT positive mutant subgroup, patients must agree to participate in the biomarker study and biopsies.
Patients must give documented informed consent to participate in this study
It is expected that five types of patients afflicted with EBV-associated lymphomas, lymphoproliferative disease or malignancies will be referred and will consent to participate in this trial; these are:
Willingness to participate in rigorous neurocognitive evaluations at baseline and serially following treatment
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must be willing to participate in all stages of treatment
Patients must be geographically accessible and willing to participate in all stages of treatment
Willing and able to consent for self to participate in study
Patients who have demonstrated resistance to platinum agents (e.g. oxaliplatin, cisplatin) are not eligible to participate in this study
Patients for whom it is not in the best interest to participate in the study, in the opinion of the treating investigator
Any other reason the investigator considers the patient should not participate in the\n             study
Signed informed consent to participate in the study, including participation in the expansion cohort after safety of enzalutamide and gemcitabine and cisplatin have been established, must be obtained from patients after they have been fully informed of the nature and potential risks by the investigator (or his/her designee) with the aid of written information
Patients with and without FLT3 mutations will be eligible to participate
Patients must give documented informed consent to participate in this study
Willing to participate in associated correlative science biomarker study
Willing to participate in associated correlative science biomarker study
Patients must be offered the opportunity to participate in the ultra pure Circulating Tumor Cells (upCTCs) study
Patients must be offered the opportunity to participate in specimen banking as outlined
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must be offered the opportunity to participate in specimen banking for future use
Written informed consent to participate in this study before the performance of any study-related procedure
Willingness and ability to consent for self to participate in study
Donor does not consent to or is unable to participate in this trial
Patients already receiving treatment with FOLFIRINOX +/- trastuzumab may participate in the study and have their data collected retrospectively if they met inclusion criteria at the start of therapy and sign consent for study participation moving forward
Signed informed consent to participate in the study must be obtained from patients after they have been fully informed of the nature and potential risks by the investigator (or his/her designee) with the aid of written information
All patients must be willing and capable to provide informed consent to participate in the protocol
Mayo Clinic Arizona only: Willing to participate in associated biobanking study, 919-04; the patient must sign consent to enroll onto the mandatory companion biobanking study in order to participate in this treatment study
Mayo Clinic Rochester and Florida only: Willing to participate in associated biobanking study, 521-93; the patient must sign consent to enroll onto the mandatory companion biobanking study in order to participate in this treatment study
Agree to participate in research blood collection at 4 different time periods (20 ml = 4 teaspoons)
Signed informed consent to participate in the study must be obtained from patients after they have been fully informed of the nature and potential risks by the investigator (or his/her designee) with the aid of written information
All patients must be willing and capable to provide informed consent to participate in the protocol
Consent to participate in Data Bank and BioRepository (DBBR) (Roswell Park Cancer Institute [RPCI] only)
Any other reason the investigator considers the patient should not participate in the study
Ability to participate in the clinical study for a minimum of at least 2 cycles (6 weeks).
Patients must give documented informed consent to participate in this study
Patients should not participate in any other therapeutic investigational study while taking part in this study
Willing and able to give informed consent and participate in study procedures as described in the 12PLK02 and 10PLK13 protocols. Patients consented for 12PLK02 will also be asked to participate in the 10PLK13 PROCLAIM registry study.
Written informed consent to participate in this study before the performance of any study-related procedure
Willingness to provide the blood specimens as required by the protocol; please note that the willingness to participate pertains only to the patient and does not factor in the institution’s ability to participate in any part of the translational component
Eligible to give informed consent to participate in the study.
PART I: Participants who have no language barrier, are cooperative, and can give informed consent before entering the study after being informed of the medications and procedures to be used in this study may participate
PART II: Participants who have no language barrier, are cooperative, and can give informed consent before entering the study after being informed of the medications and procedures to be used in this study may participate
Clinical judgement by the investigator that the patient should not participate in the study
Subjects can participate in the study if in the opinion of the investigator it is thought not to affect the subject's safety, the conduct of the study or the interpretation of the data.
Patient desires not to participate in the study.
Only one subject per household may participate
Males are not permitted to participate
KEY INFORMANT: Agrees to participate in a confidential 1-on-1 semi-structured interview with the research team
KEY INFORMANT: Unwilling to participate
Willing to consent to randomization and able to participate in the study
FOCUS GROUPS:\r\n* Has a household member who has already participated (or agreed to participate)
Those mentally or physically unable to read the consent form or other study materials and/or participate in the consent and engagement with the CaringGuidance program; women who have been hospitalized for mental health issues or substance abuse in the past year are ineligible
Have parental consent to participate
Patients must be offered the opportunity to participate in specimen banking for future research
Patients who are incompetent for interview (documented diagnosis of active psychosis or dementia) or unable to provide informed consent as assessed by the interviewer; or too sick to participate, as judged by a member of the research team or the exercise physiologist, or have been treated for another cancer
Significant uncontrolled psychiatric or other co-morbid disease, which the primary oncologist believes prohibits the ability to participate in study procedures
Adult caregivers (> 18 years) of patients who have agreed to participate in the study
(Physician participation) willing to participate in the study
Refusal to participate in the study
Able to participate safely in all program sessions
Cognitively able to consent to participate
Excluded patients will be allowed to participate in the trial on an observational basis only
Be mentally and physically able to participate in the study
PATIENT ONLY: Having a spouse/romantic partner (including same-sex) and who is willing to participate
Patient refusal to participate in randomization
Patients who are incompetent for interview (documented diagnosis of active psychosis or dementia) or unable to provide informed consent as assessed by the interviewer; or too sick to participate, as judged by a member of the research team
Children aged 14-17 will assent to participate in the research study by signing a separate assent form
INCLUSION CRITERIA FOR PARENTS: Cognitively able to participate in interactive interviews
EXCLUSION CRITERIA FOR PARENTS: Parent is cognitively or physically unable to participate in interactive interview
Physician verification of ability to participate in the intervention
Physically and cognitively able to participate in the study as determined by the investigators
HSCT CGs: Physically and cognitively able to participate in the study as determined by the investigators
Physically and cognitively unable to participate in the study as determined by the investigators
HSCT CGs: Physically and cognitively unable to participate in the study as determined by the investigators
Participants must self-identify as female; thus only women with breast cancer will be invited to participate in this study
Patients that consent to participate
Have a co-survivor (friend or family member) willing to participate in this research study
Willing to participate in yoga therapy for twelve weeks if randomized to intervention group
Unwilling to participate in yoga therapy for twelve weeks if randomized to intervention group
Willing to come to MD Anderson (MDA) for the therapy sessions; or willing to participate in the therapy sessions at their homes and live within a 45 minute drive of MDA main campus; or can participate in the therapy sessions from one of MDA’s Regional Care Centers
Caregivers with children (patients) who are younger than 10 years of age may be eligible to participate even though their children are too young to assent or participate themselves
Subject must be capable and reliable to participate in all study related procedures
Patients who refuse to participate
Be willing to provide written informed consent to participate in the study which includes several clinical evaluations, provide access to medical records/primary care physician (PCP), and allow all interviews and PSST therapy sessions to be audiotaped.
PATIENTS: Willingness to participate in all study activities including data collection
PATIENTS: Willing to identify a FCG (immediate or extended family member) to participate
FCGs: Willingness to participate in study activities including data collection
Only requirement for organ function is for patients to have competency to consent and participate in the study; in the arm of the study which requires patients to have olfactory dysfunction before enrollment, an UPSIT score will be used to identify these patients
Significant psychiatric or other co-morbid disease, which the treating clinician believes prohibits the patient’s ability to participate in the informed consent procedures
Patients who will be hospitalized to undergo first-time autologous or allogeneic BMT will be given the opportunity to assent/consent and participate in the study; with his/her permission, the patient will also be provided with their own iPad® BMT Roadmap information system to use; qualitative interviews will be conducted in patients with their assent/consent
Ability to safely participate in outpatient rehabilitation program
Unable to safely participate in outpatient rehabilitation
Too sick to participate, as determined by the treating oncologist
AYA PATIENTS ONLY: Patients that are not able to participate in the study due to their medical condition and/or treatment regimen will be excluded; such exclusion will be determined by the patients' treating oncologist in conjunction with patients' family members
All couples co-habiting for at least 3 years with current partner who is willing to participate in study
Cognitively able to participate in interactive interviews
Patient refusal to participate (any age), or parental refusal to participate for patients less than 18 years of age
Cognitively or physically unable to participate in interactive interview
Patient is willing to participate in this study
Participants with serious or unstable illness, as determined by study physicians and clinicians, may be deemed unfit to participate
Physically unable to participate in the study
have the permission of their oncologists to participate.
Willing to consent to participate
Any woman currently pregnant will not be eligible, but may participate 3 or more\n             months after the end of her pregnancy if the study is still ongoing
Have a stable partner for six months who is willing to participate
Able and willing to participate in an art therapy session at Maroone Cancer Center
Mentally and physically able to participate and complete surveys over the phone
Spouses/partners could not participate if the patient refused participation
Become unable to participate in a fully app and web-based intervention trial
Physician approval to participate in intervention
Excluded patients will be allowed to participate in the trial on an observational basis only
Patient refusal to participate in randomization
Patients must be offered the option to participate in the Diet and Lifestyle Substudy
Women who are using postmenopausal hormones, and are planning to continue the same regimen through the study intervention are eligible to participate
Individuals who are unable to participate in cycling due to musculoskeletal limitations.
Willing to participate in a weekly behavioral modification group phone call for first 3 months and every 2 weeks for the second 3 months
Willing to participate in a weekly behavioral modification group phone call for 3 months
Voluntarily agree to participate and read the informed consent documents
Multiple children from the same family are eligible to participate in the study
Patients who are being screened for the therapeutic clinical trial will also be approached for participation into the optional sub-study evaluating sociobiological response to stress; refusal to participate in the sub-study will not impact the patient’s eligibility to participate in the therapeutic intervention\r\n* Should a patient consent to the optional sub-study, the patient may proceed with the optional baseline interventions for the optional sub-study as outlined within the protocol’s study calendar
Multiple members of the same household cannot participate.
Willing to participate in all study components
Subjects consent to participate in the trial
LGBT SUB-STUDY: Participants who complete the screener, are willing to participate in a longitudinal study for one year, and who self-identify as lesbian, gay, bisexual or transgender will be eligible to participate in the cohort study
Patients must give written informed consent to participate in this study before the performance of any study-related procedure.
PARTICIPANTS: Are willing to participate in a study about health behaviors involving nutrition or CRC screening
Ability to participate fully in research elements for the duration of the trial.
general conditions in which subjects are not suitable to participate in the study
Patients who refuse to participate
Subjects who require sedation to participate will be excluded
Subjects who refuse to participate, or demonstrate inability to give informed consent
Individuals who have any of the following will not be eligible to participate:
Vulnerable patient populations:\r\n* Patients unable to participate in the consent process (children and neonates)
Willingness to participate in collection of pharmacokinetic samples
Patients who do not wish to participate
Subjects must be eligible for and willing to participate and sign consent for National Cancer Institute (NCI) protocol 08-C-0079: Natural History Study and Longitudinal Assessment of Children, Adolescents, and Adults with Neurofibromatosis Type 1, for the clinical evaluation necessary for this study
Subjects will be selected on the basis of their willingness and ability to participate and on their likelihood of completing the study
Any patient under age 18 may only participate in 3T imaging
Patients under the age of 18 may not participate in 7T imaging
Subjects who refuse to participate, or demonstrate inability to give informed consent
Patients who refuse to participate
Willing and able to consent and participate in the study.
Ability to travel to appointments and willingness to participate in this study
Patients who have been referred for CTU will also be invited to participate in the study
Patients who refuse to participate
Subjects who are willing to participate
Participant is willing to participate in the educational component of this project
OHSU Radiation Medicine department has agreed to participate as pilot department for this project; all active Radiation Medicine providers are requested to participate in the training; providers have the option to not participate
CAREGIVERS: Adult caregivers (> 18 years) of patients who have agreed to participate in study
Patients who do not verbally, written, or electronically consent to participate (usability test and RCT)
Those who do not wish to participate
Patients who refuse to participate in the study
Willingness and ability to consent for self to participate in study
A medical or psychiatric illness that precludes ability to give informed consent or is likely to interfere with the ability to comply with the protocol stipulations
Ability to give informed consent.
Ability and willingness to give informed consent.
Willingness and ability to give informed consent
Ability to give informed consent
ability to consent
Ability to give informed consent
Patients must have the ability to give informed consent
Ability to give informed consent
Patients must have the ability to give informed consent
Ability to give informed consent
Patients must have the ability able to give informed consent
Ability to give informed consent
DONOR: Ability to give informed consent
Willingness and ability to consent
Patients must demonstrate the ability and willingness to give informed consent.
Ability to give informed consent
Ability to consent
Ability and willingness to give informed consent
Ability and willingness to participate in the informed consent process and including signing a copy of the informed consent form
Ability to read and understand the informed consent form and willingness and ability to give informed consent and demonstrate comprehension of the trial before undergoing any trial activities
Ability to give informed consent
Ability and willing to give consent
Willingness and ability to give informed consent
DONOR: Ability to give informed consent
Ability to give informed consent
DONOR: Ability to give informed consent
Ability to give informed consent
Ability and willingness to give informed consent
Ability and willingness to give informed consent and ability to return to the study clinic during the study period
Ability to give informed consent
Lack of ability or willingness to give informed consent
Patients must have the ability to give informed consent
Patients must have the ability to give informed consent
Lack of ability or willingness to give informed consent.
A medical or psychiatric illness that precludes ability to give informed consent or is likely to interfere with the ability to comply with the protocol stipulations
DONOR: Ability to give informed consent
Lack of ability to give informed consent
Ability to give informed consent
Ability to give informed consent.
Ability to give informed consent
For donors >= 18 years of age, ability to give informed consent
Neurocognitive deficits that impair ability to give informed consent
Ability to give informed consent
Patients do not have the ability to give informed consent
Ability and willingness to give informed consent
Have the ability to give informed consent
Willingness and ability to give informed consent
Ability to give informed consent
Ability to understand and voluntarily sign the informed consent document
Ability to understand and voluntarily sign an informed consent form
Ability to understand and voluntarily give informed consent
Ability to understand and voluntarily give informed consent
Ability to understand and voluntarily sign an informed consent form
Ability to understand and willingness to voluntarily sign an informed consent form
Ability to understand and voluntarily sign an informed consent form
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patient has the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent.
Must have the ability to understand, and the willingness to sign, a written informed consent.
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent; all patients must have signed, witnessed informed consent prior to registration
All patients must have the ability to understand and the willingness to sign an informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to sign written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patient has the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent.
INCLUSION - ENROLLMENT: Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All research participants must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent (I-SPY TRIAL Screening Consent)
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand English language and the willingness to sign a written informed consent.
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
The ability to understand and sign informed consent
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written consent
Ability to understand and the willingness to sign a written informed consent or have parental consent
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Ability of subject to understand and the willingness to sign written informed consent for study participation.
Patients have the ability and willingness to sign written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand, and willingness to sign, the written informed consent
All research participants must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and sign informed consent
All patients must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Subjects must have the ability to understand and the willingness to sign a written informed consent; informed consent must be obtained prior to registration on the study
Ability of subject to understand, and be willing to sign informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and sign a written informed consent
Ability to understand and the willingness to sign a written protocol specific informed consent for tissue harvest or a parental/guardian informed consent and pediatric assent when appropriate.
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand, and willingness to sign, the written informed consent
Ability to understand AND willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and willingness to sign written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign an informed written consent
Patients must have the ability to understand and the willingness to sign a written consent prior to registration in the study
DOSE ESCALATION COHORT: Ability to understand and the willingness to sign a written informed consent
DOSE EXPANSION COHORT: Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability of subject to understand, and be willing to sign informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and to sign written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Patients have ability and willingness to sign written informed consent
Patient must exhibit the ability to understand and willingness to sign a written informed consent regarding the study and alternative treatments
Ability to understand and the willingness to sign a written informed consent (ICF)
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and sign a written informed consent for participation in the trial
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Ability of participant to sign a written informed consent
Patients have ability and willingness to sign written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign written informed consent
Ability to understand and the willingness to sign written informed consent and assent documents
Ability to understand and willingness to sign informed consent
Ability to understand and the willingness to sign a written informed consent
All patients must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
The ability to understand and sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Willingness to sign written informed consent to this study
Able to understand and willingness to sign a written informed consent.
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to initiation of treatment
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to sign written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent; only lucid patients qualified to consent to neurosurgical procedure will be approached for participation in this study
Ability to understand and the willingness to sign a written informed screening and treatment consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and willingness to sign written informed consent
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent
Patient has the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration in the study.
Patient able to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent; consents will be provided in English or Spanish
Ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability and willingness to understand and sign an informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All patients must have the ability and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent.
Ability to understand and willingness to sign informed consent
Ability to sign written informed consent
Ability to understand and willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
RECIPIENT: All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Willingness and ability to sign a written informed consent (assent if applicable)
All subjects must have the ability to understand and the willingness to sign a written informed consent
Subjects must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability and willingness to sign written informed consent
Ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability and willingness to understand and sign an informed consent
Ability to understand and sign informed consent.
Ability to understand and willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and willingness to sign informed consent
Ability to understand the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
All subjects must have the ability to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Ability to understand and the willingness to sign a written informed consent.
INCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Ability of subject to understand and the willingness to sign a written informed consent
Ability to understand and the willingness to sign a written informed consent; all patients must have signed, witnessed informed consent prior to registration
Ability to understand and willingness to sign informed consent
Ability to understand and the willingness to sign a written informed consent
Documented informed consent
Patients must give informed consent prior to initiation of therapy
Informed consent/assent
Execute an informed consent.
Informed consent must be obtained from all patients prior to beginning therapy, including consent for mandatory tissue submission for ERCC1 staining (and p16 staining if not locally conducted); patients should have the ability to understand and the willingness to sign a written informed consent document
Have the capacity to give informed consent
Give informed consent
Refuses to give informed consent
Informed consent for participation
Have the capacity to give informed consent
Documented informed consent of the participant
Informed consent
Informed consent
Patients must give informed consent
Informed consent
Must have the capacity to give informed consent
Informed consent must be obtained
Informed Consent
Patients must give informed consent
Informed consent
Patients must give informed consent
Informed consent
Before any study procedures are performed, subjects will have the details of the study described to them, and they will be given a written informed consent document to read; then, if subjects consent to participate in the study, they will indicate that consent by signing and dating the informed consent document in the presence of study personnel
Patients must be informed of the investigative nature of the treatment, must give appropriate informed consent to protocol procedures and must sign an Informed Consent documentation form
Understand and give informed consent
Informed consent
Documented informed consent
Understand and give informed consent
Give informed consent
Refuses to give informed consent
Informed consent
Patient's Informed Consent. -
Before any study procedures are performed, subjects (or their legally acceptable representatives) will have the details of the study described to them, and they will be given a written informed consent document to read; then, if subjects consent to participate in the study, they will indicate that consent by signing and dating the informed consent document in the presence of study personnel
Informed consent
Patients must give informed consent
Informed consent
Parental informed consent
PHASE I: For patients < 18 years, parents must give informed consent and patient must give assent; patients >= 18 must give informed consent
PHASE II: For patients < 18 years, parents must give informed consent and patient must give assent; patients >= 18 must give informed consent
Informed consent
Subjects who cannot give an informed consent
Patient must give informed consent for this new study
Consent to the study; and
Refusal of informed consent
Patients must give informed consent
Cannot give informed consent.
Willingness to give informed consent
DONOR: Willingness to give informed consent
Informed consent
Documented informed consent of the participant
Women who cannot give an informed consent in English
Willingness to give informed consent
DONOR: Willingness to give informed consent
Subjects who cannot give an informed consent
Cannot consent for himself or herself
Patients cannot give informed consent.
Patients who cannot consent for themselves
Informed consent
Informed consent
Women who cannot consent for themselves
Patients who cannot consent for themselves
Patients who cannot give informed consent
Informed consent was obtained.
Patients must have capacity to consent
Patients willing to give informed consent
Competent to sign informed consent
The patient must be competent and have signed informed consent
Competent to provide informed consent
The subject must be deemed competent to give informed consent
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign an Institutional Review Board (IRB)-approved written informed consent form
Able to understand the consent competent to sign
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
The subject must be deemed competent to give informed consent
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign an Institutional Review Board (IRB)-approved written informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent, ability to understand and willingness to sign the informed consent form
Competent to comprehend, sign, and date an IRB-approved informed consent form
Competent to give informed consent
Mentally competent, ability to understand and willingness to sign the informed consent form
Mentally competent to consent
Any participant who is not competent to provide informed consent for study participation per the investigator
Sighted and mentally competent to consent
Women competent to sign study specific written informed consent
Patients competent to sign study specific informed consent
Ability to understand and willingness to sign the consent form written in English
Ability to understand and willingness to sign the informed consent form
Ability to understand and willingness to sign a written informed consent form and comply with all study requirements
Willingness to sign the healthy volunteer informed consent form
Ability to understand and willingness to sign the consent form
Patients must sign a study-specific informed consent form prior to study entry; patients should have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign informed consent form prior to initiation of the study and any study procedures.
Ability to understand and willingness to sign an informed consent form
Ability to understand and willingness to sign the consent form
Ability to understand and willingness to sign the consent form
Ability to understand, and the willingness to sign a written Informed Consent Form
Ability to understand and the willingness to sign a written informed consent document; signed informed consent form must be obtained prior to initiation of study evaluations and/or activities
Ability to understand and willingness to sign the consent form written in English
Ability to understand and the willingness to sign a written informed consent document \r\n* Note: the consent form must be signed and dated prior to initiation of SCT preparative treatments
Ability to understand and willingness to sign the informed consent form
Ability to understand and willingness to sign informed consent form prior to initiation of the study and any study procedures
Ability to understand and willingness to sign the consent form written in English\r\n* Note: the consent form must be signed prior to the conduct of any trial-specific procedure
Ability to understand and willingness to sign a study-specific informed consent prior to study entry
Ability to understand and the willingness to sign a written informed consent document and study specific consent form prior to study entry
Ability to understand and willingness to sign the informed consent form
Have the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures
Ability to understand and willingness to sign informed consent form prior to initiation of the study and any study procedures.
Ability to understand and willingness to sign informed consent form prior to initiation of the study\r\nand any study procedures
Ability to understand and the willingness to sign a written informed consent form
Ability to understand and willingness to sign an informed consent form
Ability to understand and willingness to sign the consent form
Ability to understand and willingness to sign a written informed consent form
Ability and willingness to sign informed consent prior to any study procedure
Ability to understand and the willingness to sign a written informed consent form
Ability to understand and the willingness to participate in clinical research and comply with protocol procedures as evidenced by their signature on the informed consent form
Ability to understand and willingness to sign informed consent form prior to initiation of the study and any study procedures
Patients must sign a study-specific informed consent form prior to study entry; patients should have the ability to understand and the willingness to sign a written informed consent document
Ability to understand and willingness to sign the informed consent form
Ability to understand and willingness to sign informed consent prior to initiation of any study procedures.
Patients must have the ability to understand and the willingness to sign a written consent form
Ability and willingness to sign an informed consent form for this protocol
Ability to understand and willingness to sign an informed consent form prior to initiation of any study procedures
Ability to understand and willingness to sign an informed consent form prior to initiation of any study procedures
Ability to understand and sign informed consent form (ICF) and comply with treatment protocol
Have the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures
Ability to understand and willingness to sign informed consent prior to initiation of any study procedures;
The participant has the ability to understand and the willingness to sign a written informed consent form.
Ability to understand and willingness to consent and to sign consent form
Individuals who have the ability to understand and willingness to sign an informed consent before initiation of study procedures, after the nature of the study is explained to them and they have asked any questions
Participants must have the ability to understand, and the willingness to sign, a written informed consent form
Ability to understand and the willingness to sign an informed consent form
Subjects must have the ability to understand and the willingness to sign a written informational form
Ability to understand and willingness to sign a written informed consent form