Subjects unable to comprehend and give informed consent are excluded.
The patient must be able to comprehend and have signed the informed consent
All subjects must be able to comprehend and sign a written informed consent document
Are able to comprehend and willing to sign an informed consent form
Patients or their legal representatives must be able to comprehend and provide written informed consent
All subjects must be able to comprehend and sign a written informed consent document
Patient must be able to comprehend and sign a written informed consent and be willing to comply with all study procedures
All subjects must be able to comprehend and sign a written informed consent document
All subjects must be able to comprehend and sign a written informed consent document
Ability to comprehend the nature of the treatment
All subjects must be able to comprehend and sign a written informed consent document
All subjects must be able to comprehend and sign a written informed consent document
Patients unable to comprehend and give informed consent are excluded
Patient must be able to comprehend the approved consent document and have the willingness to sign it; the patient prior to enrollment and the administration of any protocol-specific therapy must sign the consent document
Patients must be able to comprehend and provide written informed consent
All subjects must be able to comprehend and sign a written informed consent document
Ability to comprehend and willing to sign an informed consent, assent obtained from minors
DONOR: Ability to comprehend and willing to sign an informed consent
Subject must be able to comprehend English
Able to comprehend and willing to sign the informed consent form
Informed consent: all subjects must be able to comprehend and sign a written informed consent document
Able to comprehend and willing to sign an Informed Consent Form (ICF)
Patients unable to comprehend and give informed consent are excluded
Patients unable to comprehend and give informed consent are excluded
Able to comprehend and willing to sign an informed consent form (ICF)
Able to comprehend and willing to sign informed consent form
Able to comprehend and willing to sign the informed consent form
Able to comprehend and willing to sign an Informed Consent Form (ICF)
Able to comprehend and willing to sign the written informed consent form
All patients must be able to comprehend and sign informed consent
All subjects must be able to comprehend and sign a written informed consent document
Able to comprehend and provide informed consent
All subjects must be able to comprehend and sign a written informed consent document
All subjects must be able to comprehend and sign a written informed consent document
Able to comprehend the full nature and purpose of the study, including possible risks and side effects.
DONOR: Ability to comprehend the investigational nature of the study and provide informed consent
Ability to comprehend and sign informed consent
HEALTHY VOLUNTEER: Be able to comprehend the full nature, purpose and risks of the study
Patient ability to read and comprehend the informed consent document
Subject has given written informed consent
Patient must have given written informed consent
Written informed consent
Able to give a written informed consent.
Written informed consent
Written informed consent
Written informed consent has been obtained
Has read and understands the informed consent form and has given written informed consent prior to any study procedures
Written informed consent prior to any procedure.
Provides written informed consent on the approved informed consent form
Able to give written informed consent.
Subjects given written informed consent
Written informed consent must be obtained from the patient.
Written informed consent.
Written informed consent.
Written informed consent
PRE-SCREENING: Written informed consent for prescreening
FULL STUDY INCLUSION CRITERIA: Written informed consent for full study
Written informed consent
Written informed consent for transplant
Written informed consent is given
Patient has given written informed consent.
Written informed consent
DONOR: Written informed consent
Age ? 18 years with the capacity to give written informed consent
Subjects must give written informed consent to participate in this trial
Written informed consent obtained
Written informed consent is given
Subjects given written informed consent
Subjects given written informed consent
Written informed consent for the trial
Written informed consent prior to admission to this study
Patients must give written informed consent prior to registration on the study
Written informed consent
Written informed consent
Subjects who are ?18 years of age on the date of written informed consent.
Able to give written informed consent to participate in the study
Has read and understands the informed consent form and has given written informed consent prior to any study procedures.
Written informed consent
Patient’s written informed consent
Able to give informed written consent
Written informed consent
Written informed consent
Written Informed Consent
Able to give a written informed consent.
Written informed consent for the transplant phase
Written informed consent
Patient must give written informed consent
Written informed consent is given
Obtained written informed consent
Written informed consent must be obtained before any assessment is performed.
Written informed consent to participate in this study
Patient must give written informed consent
Written informed consent prior to any procedure
Subjects must give written informed consent to participate in this trial
Written informed consent must be obtained
Written informed consent
Written informed consent
Written informed consent.
Written informed consent must be obtained from all patients before entry into the study
Written informed consent
Written informed consent has been obtained
Written informed consent
Written informed consent
Written informed consent prior to registration on study
Has given written Informed Consent
Patients must give written informed consent
Written informed consent
Written informed consent and assent as is age appropriate
Written informed consent
Written Informed Consent
Written informed consent
Written informed consent or assent
Has given written informed consent.
Written informed consent
Subjects must give written informed consent to participate in this trial
Able to give informed written consent
Written informed consent;
patient had given written informed consent.
Written informed consent obtained before undergoing any study-related activities
Has the subject given written informed consent?
Written informed consent has been obtained
Patients who give a written informed consent
Written informed consent.
Capable of given written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Patients must give written informed consent
Subjects must have given written informed consent to agree to participate
Subjects must have given written informed consent
Written informed consent and any locally required authorization
Subjects given written informed consent.
Written, informed consent
Written informed consent.
Documented written informed consent of the participant
Able to give written informed consent
HSCT CGs: Able to give written informed consent
Written, informed consent
Written informed consent
Must give written study consent
Any patient with cholestasis due to suspected MHO who provides written informed consent.
Properly obtained written informed consent
Gives written informed consent
Gives written informed consent
All patients to give written informed consent to participate
Written informed consent
Adequately informed of the nature and risks of the study with written informed consent
Give written informed consent
Properly obtained written informed consent
Able to perform written, informed consent
Written consent
Written informed consent
Given written informed consent (patient and donor)
Written informed consent obtained from the subject.
Written informed consent obtained from the subject
Patient provides written informed consent
Written informed consent
Give written informed consent
Patient provides written informed consent
Patient provides written informed consent
Patients must give written informed consent
Able to give written informed consent to participate in the study
Provides written informed consent
Provides written informed consent document
Patients who have granted written informed consent for the study
Written informed consent will be obtained from patients
Provides written informed consent
Written informed consent
Provides written informed consent
Written informed consent
Written informed consent
Provides written informed consent
Provides written informed consent
Written informed consent
All patients must give written informed consent
Written informed consent.
Provides written informed consent
PIK3CA WILD TYPE COHORT (closed 03/17/2016): Able to understand and willing to sign an IRB-approved written informed consent document
Patients must give IRB approved, study specific, informed consent.
INCLUSION CRITERIA FOR REGISTRATION (HER2 MUTATION IDENTIFIED BY WASH U GPS LABORATORY): Able to understand and willing to sign an IRB approved written informed consent document
INCLUSION CRITERIA FOR REGISTRATION (HER2 MUTATION IDENTIFIED AT AN OUTSIDE CLIA CERTIFIED LOCATION): Able to understand and willing to sign an IRB approved written informed consent document
ARM 2 - A: Able to understand and willing to sign an IRB-approved written informed consent document
Patients must sign IRB approved study specific informed consent.
Able to understand and willing to sign an IRB-approved written informed consent document
Donor must be able to understand and willing to sign an IRB approved written informed consent document. Recipient Inclusion Criteria
Recipient must be able to understand and willing to sign an IRB approved written informed consent document.
Able to understand and willing to sign an IRB-approved written informed consent document
Surgeon: Able to understand and willing to sign an IRB-approved written informed consent document
Nurse: Able to understand and willing to sign an IRB-approved written informed consent document
Able to understand and willing to sign an IRB-approved written informed consent document
Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to step 1 registration
Patient must provide study specific informed consent prior to study entry, including the mandatory pre-treatment plasma EBV DNA assay
Patients must provide study specific informed consent prior to study entry, including consent for mandatory tissue submission for central review
Patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
All patients must sign study specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patients must sign a study-specific informed consent form prior to study entry
The patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry; no durable power of attorney or next of kin can provide initial consent
Patients must provide study specific informed consent prior to study entry
Patient must capable of, and provide, study specific informed consent prior to study entry
All patients must sign study specific informed consent prior to study entry or within 1 week of first treatment, provided other criteria were met
Patient signs study specific informed consent prior to study enrollment
Did the patient provide study-specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Subject must sign a study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patients must give study specific informed consent prior to enrollment
Patient must sign study specific informed consent prior to study entry
Patient must have provided study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry, including consent for mandatory submission of tissue for required, central p16 review
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study registration
The patient must provide study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patients must sign study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry, including consent for mandatory tissue submission for EGFR and for oropharyngeal patients, HPV analyses
Patients must sign a study-specific consent form prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must capable of and provide study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Must provide study-specific informed consent prior to study entry
The subject must provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry, including consent for mandatory screening of tissue
Patients must provide study-specific informed consent prior to study entry
Patients must sign a study-specific informed consent form prior to study entry
The patient must sign specific informed consent prior to study entry
The patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry/screening
Patient must provide study specific informed consent prior to study entry.
Subject must sign a study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to registration
Patients must provide study specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to study entry
Patient must be capable to read and speak English and provide study specific informed consent prior to study entry
SPECIFIC TO STUDY PART #1
SPECIFIC TO STUDY PART #2
Patient must sign study-specific informed consent prior to study entry
Patient must sign study-specific informed consent prior to study entry
Subject must sign a study specific informed consent prior to study entry
The patient must have capacity to be able to sign a study-specific informed consent prior to study entry
Patients must be capable to read and speak English and provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Able to understand and sign the informed consent document
Age >18 and must be able to read, understand, and sign informed consent
Patients must be able to understand and sign informed consent form
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Patients must be able to understand and give informed consent
Able to understand and sign the informed consent document
Able to understand and sign informed consent
Subject can understand and sign the informed consent document, can communicate with the investigator, and can understand and comply with the requirements of the protocol.
Patients are able to understand and willing to sign the informed consent.
Able to understand and willing to sign informed consent
Able to understand and sign the Informed Consent Document
Able to understand and sign the informed consent document
Able to understand and sign informed consent
Able to understand and sign the informed consent document
Subjects who are able to understand and sign an informed consent document
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Patients must be able to understand and sign an informed consent form
Able to understand and sign the informed consent document
Able to understand and sign informed consent
Able to understand informed consent
DONOR: Able to understand and sign informed consent
The patient is able to understand and give informed consent
Able to understand and sign the informed consent document
Patient and/or responsible person able to understand and sign consent
Patient and/or responsible person able to understand and sign consent
Patients must be able to understand and give informed consent
Patients must be able to understand and sign the informed consent
Able to understand and sign an Informed Consent
Able to understand and sign the informed consent document
Patients must be able to understand and willing to sign an informed consent
Able to understand and sign the informed consent document
Able to understand and sign informed consent
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Patients must be able to understand and sign informed consent
Able to understand and give informed consent
Patient must be able to understand and willing to sign an informed consent
Able to understand and sign the informed consent document
Able to understand and sign informed consent
Patients must be able to understand and willing to sign an informed consent
Must be able to read, understand and sign informed consent
Patients must be able to understand and sign informed consent
Able to understand and sign informed consent
DONOR: Donors must be able to understand and sign informed consent
Able to understand and sign the informed consent document
Must be able to understand and sign the informed consent document
Able to understand and sign the Informed Consent document
Be able to understand and sign informed consent
Able to understand and sign informed consent
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Adults must be able to understand and sign the informed consent document
Patients must be able to read, understand and sign informed consent
Able to understand and sign the informed consent document
Able to understand and sign the informed consent document
Able to understand and sign the Informed Consent Document
Able to understand and sign the informed consent document
Able to understand and sign the informed consent
Subjects who are able to understand and sign an informed consent document
Able to understand and sign the informed consent
Able to understand and sign consent
Subjects must be willing and able to understand and sign informed consent
Patients must be able to understand and willing to sign an informed consent
Patients must be able to understand and willing to sign an informed consent
Able to understand and sign an informed consent document (or has a legal representative who is able to do so)
Willing to sign Informed Consent;
Able to sign an informed consent
Sign informed consent.
Willing and able to sign informed consent
Ability to sign an informed consent; can be signed by family member or health care proxy; informed consent must be done prior to registration on study
Willingness to sign informed consent
Ability to sign informed consent
Able to sign informed consent
Patient refuses to sign informed consent
Patients must be willing and able to sign informed consent for themselves
Patients must be willing to sign the protocol-specific written informed consent
Refusal to sign the informed consent
Refusal to sign the informed consent
Refusal to sign informed consent
Able to sign informed consent
Able to sign informed consent
All subjects must sign a written informed consent
Patient able to sign informed consent
Sign an informed consent document
Patients must sign an informed consent document
Patients willing and able to sign consent
All subjects must sign a written informed consent
Patients must sign informed consent prior to study entry
Refusal to sign the informed consent
Patients must sign informed consent
Patient is able to give and sign study specific informed consent
Able to sign informed consent
Patients must sign an informed consent
Subjects must understand and sign the study specific informed consent
Subjects must freely sign informed consent to enroll in the study
Patients must sign the informed consent document
Must sign informed consent
Patients must sign study specific informed consent
Patients must sign an informed consent
Patient must be willing to sign informed consent
Patients must be willing and able to sign informed consent
Patients must be willing and able to sign informed consent
Willing and able to sign informed consent
Must be willing to sign a written informed consent.
Patients must sign a written informed consent prior to entering the study.
All patients must sign an informed consent prior to enrollment.
Patients must sign an informed consent document
Patients must sign an informed consent document
Refusal to sign informed consent
Patients must sign informed consent
Patients must sign informed consent
Patients must sign informed consent
Failure to sign informed consent
Patients must sign an approved informed consent document
Willing and able to sign informed consent
Patients who are not able to sign inform consent
All patients must sign informed consent
Patient refuses to sign informed consent
Patient must sign the informed consent document
Patients must sign an informed consent
Subject must understand and sign the study specific informed consent
Patient refuses to sign informed consent
Willing and able to sign informed consent
Patients must sign informed consent prior to study entry
Patients must sign written informed consent
Patient is willing to sign study specific informed consent
Able to sign an informed consent
TREATMENT: Patients must be willing to sign the standard informed consent
Must sign an approved informed consent
All patients must sign a written informed consent
All patients must sign an informed consent prior to enrollment
Refusal to sign informed consent
Patients must be capable and willing to sign informed consent
Patients must be willing to sign an informed consent
Patients or guardian able to sign informed consent
Patient is able to give and sign study specific informed consent
Must sign a written informed consent,
Both parties are required to sign an informed consent
Patients must sign written informed consent
Potential participant/guardian is willing to sign informed consent
Patient and/or parents/guardians as appropriate must sign an informed consent, be mentally responsible, able to understand and willing to sign a written informed consent
Individual is willing to sign written informed consent
Willing to sign consent
Patients must sign an informed consent
The patient must sign consent for study participation
Able to sign informed consent
Subjects must sign informed consent
Patients refusing to sign informed written consent for participation in research
All patients must sign a written informed consent
Willing to sign informed consent
Patients must be able to sign informed consent
Patients must sign an informed consent before data collection, screening, or initiation of study procedures
Patients sign the informed consent
Ability to sign informed consent
Patients must sign an informed consent, and be mentally responsible
Sign informed consent
Ability to sign an informed consent
Subjects who refuse to give and/or sign the informed consent
Patients who agree to sign an informed consent to undergo MBI
Refusal to sign the informed consent
Ability to sign informed consent
Patient must sign informed consent to participate in the study
The patient does not sign the informed consent
Patients must sign an informed consent document
Patients must sign an informed consent
Ability of a patient or a Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document
The patient or a legally authorized representative must provide study-specific informed consent prior to step 1 registration
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry.
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
Patients or their legally authorized representative must provide written informed consent
Ability to understand and the willingness to sign a written informed consent document; if a patient has impaired decision-making capacity, a legally authorized representative, patients will be allowed to participate
The subject or the subject's legally acceptable representative provides written, informed consent prior to the initiation of any study procedures.
Documented informed consent of participant and/or legally authorized representative
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
Ability to understand and/or the willingness of their parent or legally authorized representative to sign a written informed consent document
Ability of subject or legally authorized representative to understand and the willingness to sign a written informed consent document
DONOR: Ability of subject or legally authorized representative to understand and the willingness to sign a written informed consent document; medically fit and willing to donate
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
Must sign study-specific, IRB approved informed consent form prior to study entry. Note consent by legally authorized representative is not allowed for this trial.
Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
Ability to understand and the willingness to sign a written informed consent document. Patients with Impaired Decision Making Capacity (IDMC) can have a Legally Authorized Representative sign on their behalf. Documentation, such as a Power of Attorney, must be presented in order for a substitute decision maker to be allowed
Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.
The participant (or legally authorized representative, if applicable) must be willing and able to provide written informed consent for the trial
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document; for subjects < 18 years old their legal guardian must give informed consent; pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those > 7 years of age, when appropriate
Documented informed consent of participant and/or legally authorized representative
Ability of subject or legally authorized representative (LAR) to understand and sign the written informed consent document
Ability of patient or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
The patient or legally authorized representative must provide study-specific informed consent prior to study entry
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
Patients or appropriate legally authorized representatives must possess the ability to give informed consent
Documented informed consent of the participant or legally authorized representative
Patient must have the ability to understand the requirements of the study and signed informed consent. A signed informed consent by the patient or his legally authorized representative is required\r\nprior to their enrollment on the protocol
Patients or their legally authorized representative must provide written informed consent
Documented informed consent of the participant and/or legally authorized representative
Documented informed consent of the subject and/or legally authorized representative
Subject or subject's legally acceptable representative has provided informed consent.
Patients or their legally authorized representative must provide written informed consent
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
Able to understand the potential risks, benefits, and requirements of the study and are willing to provide informed consent; an informed consent form for this study that is signed by the patient or his/her legally authorized representative is required prior to enrollment
Able to understand the potential risks, benefits, and requirements of the study and are willing to provide informed consent; an informed consent form for this study that is signed by the patient or his/her legally authorized representative is required prior to enrollment
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must have the ability to understand and provide signed informed written consent
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Patient or legally authorized representative able to sign informed consent
Patients or their legally authorized representative must provide written informed consent
Patient, legally authorized representative (LAR), or parent able to sign informed consent; able to give assent for patients age 7-17
Patient must have the ability to understand the requirements of the study and signed informed consent a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
Participant has the ability and the willingness to sign the informed consent document (for adults only, for participants with mild cognitive abilities may use a legally authorized representative)
Patient or legally authorized representative able to sign informed consent
RECIPIENT: Ability of subject or legally authorized representative (LAR) (if the patient is deemed by the treating physician to be cognitively impaired or questionably impaired in such a way that the ability of the patient to give informed consent is questionable) to understand and the willingness to sign a written informed consent document indicating that they are aware of the investigational nature of this study or written informed consent obtained from parent or legal guardian if subject is a minor
Must sign study-specific, IRB approved informed consent form prior to study entry. Note consent by legally authorized representative is not allowed for this trial.
Patient or legally authorized representative able to sign informed consent
Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
Ability to understand and the willingness to sign a written informed consent document; if the subject is unable to understand the consent due to comorbidity, such as Alzheimer’s disease, consent by a legally authorized representative and assent by the subject will be obtained
Signed informed consent by the patient or legally authorized representative
Voluntary written consent (adult or legally authorized representative; or parental/guardian)
Patient or legally acceptable representative has granted written informed consent before any study specific procedures (including special Screening tests) are performed
Cases involving subjects who are minors, pregnant or require an authorized representative for informed consent
Documented informed consent of the participant and/or the legally authorized representative
Documented informed consent of the participant and/or legally authorized representative
Patient or legally authorized representative able to sign informed consent
Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
The patient or a legally authorized representative must provide study-specific informed consent prior to study registration
The patient or a legally authorized representative must provide study-specific informed consent prior to step 1 registration
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry, including consent for mandatory tumor tissue, serum, and blood submission for immune correlatives (all patients) and p16 analysis (oropharyngeal cases only)
Subjects must be able to understand the nature of this trial and provide written informed consent, prior to any study specific procedures; patients with Impaired Decision Making Capacity (IDMC) who have a close caregiver or legally authorized representative (LAR) may be considered eligible for this study at the treating physician’s discretion, provided that the physician is reasonably sure that the possible risks and benefits of the study are clear and that the patient will take the drug as prescribed
Ability to understand and the willingness to sign a written informed consent document or patients with Impaired Decision Making Capacity (IDMC) if they are represented by a Legally Authorized Representative (LAR)
The participant (or legally acceptable representative if applicable) provides written informed consent for the trial
Patient (or his or her legally accepted representative) has provided written informed consent to participate in the study
Ability to understand and the willingness to sign a written informed consent document (either directly or via a legally authorized representative)
Ability to understand and the willingness to sign a written informed consent document (either directly or via a legally authorized representative)
Subject or his/her legally authorized representative or guardian understands and voluntarily signs an informed consent document prior to any study related assessments/procedures are conducted (except as noted in Section 6).
The patient or a legally authorized representative must provide study-specific informed consent prior to step 1 registration
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
Subject or Authorized Representative is unable to provide informed consent.
Patients or their legally authorized representative must provide written informed consent
Be willing and able to provide written informed consent/assent for the trial; consent may be obtained by legally authorized representative (LAR) according to the protocol
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Either the subject or his/her legally authorized representative be willing and able to provide written informed consent for the trial
Able to understand and willing to sign a Human Research Protection Office (HRPO) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and/or the willingness of participant or their parent/legally authorized representative to sign a written informed consent document
Subject must be able to understand and willing to sign an informed consent. A legally authorized representative may consent on behalf of a subject who is otherwise unable to provide informed consent, if acceptable to and approved by the site and/or site's Institutional Review Board (IRB).
Written informed consent, Release of Medical Records Form and HIPAA reviewed and signed by patient or legally authorized representatives
Ability to understand and the willingness to sign a written informed consent document; if the subject is unable to understand the consent due to comorbidity, such as Alzheimer’s disease, consent by a legally authorized representative and assent by the subject will be obtained
PRE-REGISTRATION INCLUSION CRITERIA: Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
The patient must be willing and able to comply with all study protocol requirements. The patient or a legally authorized representative must fully understand all elements of the informed consent and have signed the informed consent according to institutional and federal regulatory requirements
Ability of the patient (or legally authorized representative if applicable) to understand and the willingness to sign a written informed consent document.
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
Able to give informed consent, or their legally authorized representative can give informed consent
Patient, or his/her legally authorized representative, is able to understand and provide informed consent.
Patient or a legally authorized representative of a patient must be able and willing to sign informed consent document that has been approved by an IRB
Patients or their legally authorized representative must provide written informed consent
A written and voluntarily signed informed consent must be obtained from the patient or legally authorized representative, in accordance with local regulations, before the initiation of any study related procedures. The patient or legally authorized representative must be able to read and understand the informed consent form (ICF).
Patient or legally authorized representative able to sign an informed consent form
Patient or legally authorized representative able to sign informed consent
A written and voluntarily signed informed consent must be obtained from the patient or legally authorized representative, in accordance with local regulations, before the initiation of any study related procedures. The patient or legally authorized representative must be able to read and understand the informed consent form (ICF).
Documented informed consent of the participant and/or legally authorized representative
Patients or their legally authorized representative must provide written informed consent
Able to provide informed consent, or if the oncology physician determines the patient to not have decision-making capacity, a patient-designated health care proxy (or authorized representative per institutional policies) must sign consent by the baseline visit; if the participant is found to be impaired on the Blessed-Orientation Memory Concentration Test (BOMC) during screening; they must have a health care proxy or authorized representative to be eligible to enroll
The patient or a legally authorized representative must provide study-specific informed consent prior to study entry
102 Subject or subject's legally acceptable representative has provided informed consent/assent prior to initiation of any study-specific activities/procedures.
Ability to understand and/or the willingness of the patient (or parent or legally authorized representative, if minor) to provide informed consent, using an institutionally approved informed consent procedure
Ability of subject or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document
SUBJECT: Ability of subject or Legally Authorized Representative (LAR) to understand and willingness to sign a written informed consent document.
Documented informed consent of the participant and/or legally authorized representative
Legally authorized representative consent
Before any study-specific procedure, the appropriate written informed consent must be obtained from the subject or a legally accepted representative.
Subject or authorized representative has provided informed consent.
Participant/parent/legally authorized representative (LAR) unwilling to give written informed consent
Decisionally impaired adults requiring a legally authorized representative
Voluntary written consent signed by the subject (or the subject’s legally authorized representative)
Ability to understand and the willingness to sign a written informed consent document; a legally authorized representative (LAR) may sign informed consent for persons who do not have the capacity to legally consent to take part in the study
Ability of the subject, or the legally authorized representative (LAR) if the patient is deemed by the treating physician to be cognitively impaired or questionably impaired in such a way that the ability of the patient to give informed consent is questionable, to understand, and the willingness to sign, a written informed consent.
Subject or legally authorized representative signs study-related informed consent document
Patient or the patient’s legally authorized representative must provide written informed consent prior to registration and any study-related procedures
Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
Valid informed consent by subject or subject’s legally authorized representative (LAR)
Patient or patient's legally acceptable representative cognitively provides written informed consent
Patient, or authorized representative signs a written Informed Consent form to participate in the study, prior to any study mandated determinations or procedure
Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
Ability of subject or legally authorized representative (LAR) (if the patient is deemed by the treating physician to be cognitively impaired or questionably impaired in such a way that the ability of the patient to give informed consent is questionable) to understand and the willingness to sign a written informed consent document indicating that they are aware of the investigational nature of this study
Patient or the patient’s legally acceptable representative must provide written informed consent prior to registration and any study-related procedures
Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
Patient, or authorized representative signs a written Informed Consent form to participate in the study, prior to any study mandated determinations or procedure
Participant must be aware of the nature of her malignancy, understand the study requirements and risks and be able and willing to sign a written informed consent document
Subject must be able to understand and be willing to sign a written informed consent document
Participant is able to understand and comply with study requirements and is willing to sign a written informed consent document
Able to understand and willing to sign written informed consent.
Patient must be able to understand and willing to sign a written informed consent document
Subject must sign a written informed consent document
Able to understand, and willing to sign, a written informed consent document.
Patient must be able to understand and willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Ability to understand and willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Able to understand and willing to sign a written informed consent document
Patients must be willing and able to understand the informed consent document
Able to understand, and willing to sign a written informed consent document
Patient must be able to understand and be willing to sign a written informed consent document
Patients must be able to understand and be willing to sign a written informed consent document
Patients must be able to understand and sign a written informed consent document and complete study-related procedures and questionnaires
Able to understand and sign a written informed consent document.
Patients must be able to understand and be willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
Subjects must be able to understand and be willing to sign a written informed consent document
Be able to understand and be willing to sign a written informed consent document
The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
Participants must be able to understand and willing to sign a written informed consent document
Patients must be able to understand and willing to sign a written informed consent document
Patients must be able to understand and willing to sign a written informed consent document
Patient needs to be able to understand and demonstrate willingness to sign a written informed consent document
AMKL PATIENTS: Patients must be able to understand and willing to sign a written informed consent
MF PATIENTS: Patients must be able to understand and willing to sign a written informed consent
Patient needs to be able to understand and demonstrate willingness to sign a written informed consent document
Patients must be able to understand and be willing to sign a written informed consent document.
Ability to understand and willing to sign a written informed consent document
The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
Patients able to understand and willing to sign a written informed consent documents
Participants must be able to understand and be willing to sign a written informed consent document
Patients must be able to understand and willing to sign a written informed consent document.
Patient must be able to understand and willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Able to understand and willing to sign written informed consent document
Patients must be able to understand and be willing to sign a written informed consent document
Able to understand and to sign a written consent document
Patients must be able to understand and be willing to sign a written informed consent document
Patients must be able to understand and willing to sign a written informed consent document
RECURRENT/ PROGRESSIVE DIPG (STRATUM 1): The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
NON-PROGRESSED DIPG (STRATUM 2): The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
Patient must be able to understand and be willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Patients must be able to understand and be willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Ability to understand and willing to sign a written informed consent document
Ability to understand and willing to sign a written informed consent document
Able to understand and willing to sign a written informed consent document
The ability to understand and be willing to sign an informed consent document
Able to understand and willing to sign a written informed consent document
Participants must be able to understand and willing to sign a written informed consent document
Participants must be able to understand and be willing to sign a written informed consent document
Patients must have the ability to understand English, sign a written informed consent document, and be willing to follow protocol requirements
The patient understands the study requirements and is willing and able to sign an informed consent document
Sign a written informed consent document
Participants must be able to understand and willing to sign a written informed consent document
Patient must be able to understand and willing to sign a written informed consent document
Ability of subject to understand and willing to sign a written informed consent document
AIMS 1 AND 2: Participants must be able to understand and willing to sign a written informed consent document
AIM 3: Participants must be able to understand and willing to sign a written informed consent document
Able to understand and willing to sign a written informed consent document
Able to understand and willing to sign a written informed consent document
Must be able to understand and sign a written informed consent document
Patients must be able to understand and be willing to sign a written informed consent document to participate
Patients who are able to understand the investigational nature of this study and agree to sign a written informed consent document
Unwillingness to give written informed consent
Unwillingness to undergo RPFNA
Inability or unwillingness to give informed consent
Inability or unwillingness to swallow
Noncompliance - inability or unwillingness to comply with medical recommendations regarding therapy or follow-up, including smoking tobacco
Unwillingness to be transfused with blood components
Unwillingness or inability to given written informed consent.
Inability or unwillingness to sign the informed consent form.
Inability or unwillingness to tolerate endocrine therapy
Inability or unwillingness to have pleural catheter placed
Inability or unwillingness to receive antithrombotic therapy
Unwillingness or inability to receive conventional chemotherapy
Regular use of thiazide diuretics (i.e., hydrochlorothiazide), which can lead to hypercalcemia, and unwillingness or inability to discontinue or switch to alternative anti-hypertensive agent
Unwillingness to maintain adequate contraception measures for the entire course of the study
Inability or unwillingness to take folic acid, vitamin B12 supplementation or corticosteroids
Inability or unwillingness to take folic acid or vitamin B12 or dexamethasone
Unwillingness to stop calcium supplementation (during the first cycle of treatment) or vitamin D supplementation throughout the study
Unwillingness to stop calcium supplementation
Unwillingness to be transfused with blood components.
Failure/inability/unwillingness to provide names and contact information for two family members or friends to serve as emergency contacts during the course of the study
Inability or unwillingness of individual to give written informed consent
Unwillingness or inability to cooperate, or, for the parents or guardians of minors, to give consent, or for the child to give assent, or any condition of sufficient severity to impair cooperation with the study
Inability or unwillingness to give informed consent
Inability or unwillingness of individual to give written informed consent
Inability or unwillingness to abstain from non-protocol use of aspirin or NSAIDs or to provide blood, urine, or stool samples or colon biopsies during the study
Unwillingness to prevent pregnancy during the medication phase and 1 month afterwards (women only)
Unwillingness or inability to participate or give informed consent
Inability or unwillingness of patient, parent, or guardian to consent
Inability or unwillingness to provide informed consent to the study
Inability or unwillingness to undergo PET scanning
Inability or unwillingness to cooperate with requirements of this trial
Inability or unwillingness to undergo the complete series of imaging sessions; inability or unwillingness to complete the one month follow-up
Unwillingness or inability to give informed consent
Regular use of thiazide diuretics (i.e., hydrochlorothiazide), which can lead to hypercalcemia, and unwillingness or inability to discontinue or switch to an alternative anti-hypertensive agent
Unwillingness to engage in adequate contraception
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent.
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
Each patient’s parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
Patients or legal guardians must sign an informed consent indicating that they are aware this is a research study and have been told of its possible benefits and toxic side effects; patients or their guardians will be given a copy of the consent form
All participants and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must have the ability to understand and the willingness to sign a written informed consent
All patients >= 18 years of age must sign a written informed consent; for patients < 18 years old, the patient’s parents or legal guardians must sign a written informed consent, unless the patient is an emancipated minor; childhood assent, when age appropriate as per institutional guidelines, should be signed by the participating patient
Patients and/or their parents or legal guardians must be capable of understanding the investigational nature, potential risks and benefits of the study; all patients and/or their parents or legal guardians must sign a written informed consent
All participants and/or their parents or guardians must sign a written informed consent.
All patients and/or their parents or legal guardians must have the ability to understand and the willingness to sign a written informed consent
Legal guardians must sign an informed consent indicating that they are aware of this study, the possible benefits, and toxic side effects; legal guardians will be given a signed copy of the consent form
A written informed consent MUST be obtained from the patients and/or their parents/legal guardians prior to enrollment indicating their awareness of investigational nature of this study
Patients or legal guardians must sign an informed consent indicating that they are aware this is a research study and have been told of its possible benefits and toxic side effects; patients or their guardians will be given a copy of the consent form
Patients (parents/guardians for those < 18) and donors must be able to sign consent forms
All patients and/or their parents or legal guardians must sign a written informed consent
Patients or legal guardians must sign an informed consent indicating that they are aware this is a research study and have been told of its possible benefits and toxic side effects; patients or their guardians will be given a copy of the consent form
Written informed consent by patients and/or their parents or legal guardians; assent for those patients inclusive of ages 12 to 17
Signed informed consent form by patients and/or patients' parents/legal guardians and age appropriate assent form by the patients obtained before any study specific procedure
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
Patients or legal guardians must sign an informed consent indicating that they are aware this is a research study and have been told of its possible benefits and toxic side effects; patients or their guardians will be given a copy of the consent form
All patients and/or their parents or legal guardians must sign a written informed consent
Patients or legal guardians must sign an informed consent indicating that they are aware this is a research study and have been told of its possible benefits and toxic side effects; patients or their guardians will be given a copy of the consent form
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
Signed informed consent from patients and/or their parents or legal guardians
All patients and/or their parents or legal guardians must sign a written informed consent
Signed informed consent from patients and/or their parents or legal guardians
Patients and/or their parents or legal guardians must be capable of understanding the investigational nature, potential risks and benefits of the study. All patients and/or their parents or legal guardians must sign a written informed consent.
All patients, or their legal guardians, must sign a written informed consent in accordance with institutional guidelines
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent (patient assent is also recommended when applicable according to each institution’s policy)
CO-PARENTS
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent (patient assent is also recommended when applicable according to each institution’s policy)
All patients and/or their parents or legal guardians must sign a written informed consent
All patients and/or their parents or legal guardians must sign a written informed consent
CAREGIVER/PARENT: Caregivers (parents or legal guardians) must give informed consent
Written informed consent signed by all patients and/or their parents or legal guardians (both parents/guardians if reasonably available)
Able and willing to give informed consent
Patients must be able to give adequate informed consent
Able to give informed consent
TREATMENT: Patient able to give informed consent
Patients must be able to give informed consent
Patients who are able to give informed consent
Willing and able to give informed consent
Able to give informed consent
Willing and able to give informed consent
Donors must be able to give informed consent
Able to give informed consent
Able to give informed consent
Subjects must be able to give informed consent
Be able to give informed consent
Able to give informed consent
Patient able to give informed consent
Be able to give informed consent
TREATMENT: Patient able to give informed consent
Be able and willing to give informed consent
Patients should be willing and able to give informed consent
Patients are willing and able to give informed consent (Phase II only)
DONOR: Able to give informed consent
Willing and able to give informed consent
Able and willing to give informed consent.
Able to give informed consent
Able to give informed consent
patients who are able to give informed consent
Able to give informed consent
Able to give informed consent
Willing and able to give informed consent
Able and willing to give informed consent.
Able and willing to give informed consent.
Able to give informed consent.
Able to give informed consent
Willing and able to give informed consent.
Willing and able to give informed consent.
Willing and able to give informed consent
Patients must be able to give informed consent
Patients must be able to give informed consent
Able to give informed consent
Willing and able to give informed consent and adhere to protocol therapy
Willing and able to give informed consent
Subjects must be able to give informed consent
Able to give informed consent
ELIGIBILITY FOR ENROLLMENT/SCREENING (ARMS 1 AND 2): Patients must be able to give informed consent
Willing and able to give informed consent
Willing and able to give informed consent
Able to give informed consent
Able to participate in the informed consent process
Patients must be able to give informed consent
Able to give informed consent.
Be able to give informed consent
Able to give informed consent
Willing and able to give informed consent
Patient must be able to give informed consent
Patients must be able to render informed consent and must consent to participate in the trial
Able to give informed consent
Able to give consent
Able to give informed consent
PARTNER: Able to consent to the study
Able and willing to give informed consent
Able and willing to give informed consent
Able to give informed consent
Able to give informed consent
Able to give informed consent
Are able to give consent
Participants are able to give consent
Participants are eligible if they are able to give consent
Are eligible if they are able to give consent
Patients and caregivers must both be able to give informed consent
Able to give informed consent
Subjects are able to give informed consent
Able to give informed consent
Able to give informed consent
Able to give informed consent
Able to give informed consent
Able to give consent
Able to consent for the study
All subjects must be able to give informed consent
Patients/subjects able to give informed consent
Patient is able to give informed consent for this study
Subject is able to give informed consent for this study
Able to give informed consent
Patient must be able and willing to give informed consent
Able to give informed consent
Able to give consent
Women who are not able to give consent
Willing and able to give informed consent
The patient must be able to give informed consent
Evidence of a signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the study
Show evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial.
Evidence of a personally signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the study
Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study
Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment.
Ability to understand and willingness to sign a written informed consent document indicating that the patient has been informed of all pertinent aspects of the trial prior to enrollment
Signed and dated informed consent form indicating that the patient has been informed of all pertinent aspects of the trial prior to enrollment
Signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the trial prior to randomization
Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment
Provide signed and dated informed consent indicating that the patient has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.
Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
Must provide a signed and dated informed consent indicating that the participants has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.
Signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to undergoing study screening procedures
Signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
Evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial
Signed and dated informed consent indicating that the subject (or legally acceptable representative if applicable by local laws) has been informed of all the pertinent aspects of the trial prior to enrollment
Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment
Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
A personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial
Subjects must be willing and able to sign the informed consent and comply with the study protocol.
Able to agree to and sign informed consent and to comply with the protocol
Able to understand and voluntarily sign the ICF and able to comply with the study visit schedule and the other protocol requirements.
Willing and able to comply with the protocol and sign informed consent
Patient has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements
Patient has signed the informed consent prior to any screening procedures being performed and is able to comply with the protocol requirements
Able to understand and voluntarily sign the informed consent form, and able to comply with the study visit schedule and other protocol requirements; written informed consent obtained prior to any screening procedures
Able to understand and voluntarily sign a written informed consent, and willing and able to comply with protocol requirements
Able to understand and voluntarily sign a written informed consent, and willing and able to comply with protocol requirements
Ability to understand and the willingness to sign a written informed consent document; subject has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements
Capability to understand and comply with the protocol requirements as and signed informed consent documents
Capable of understanding the protocol requirements, is willing and able to comply with the study protocol procedures, and has signed the informed consent document.
Patient has signed informed consent and is willing to comply with the protocol
Patients must be willing and able to give written informed consent prior to any protocol-specific procedures being performed and comply with the protocol requirements for the duration of the study.
Ability to understand and the willingness to sign a written informed consent document; subject has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements
Patient has signed the informed consent form prior to the performance of any screening procedures and is able to comply with protocol requirements.
Patient has signed the Informed Consent Form (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements
Patient has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirement
Willing and able to sign written informed consent and be able to comply with the study protocol for the duration of the study
Patient has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements.
Patient must be able to give informed consent and comply with the treatment protocol and follow-up plan.
Able to understand and voluntarily sign the informed consent form, and able to comply with the study visit schedule and other protocol requirements
Able to sign informed consent and to comply with the protocol
Willing and able to comply with the protocol and sign informed consent
able understand and give written informed consent and comply with the study protocol.
Patients must be willing and able to provide signed informed consent and comply with the study protocol.
Willing and able to sign the informed consent and to comply with the protocol for the duration of the study.
Able to sign informed consent and to comply with the protocol
Able to sign informed consent and to comply with the protocol
Able to understand and comply with the protocol requirements and has signed the informed consent document.
Patients able to render informed consent and to follow protocol requirements
Willingness to sign informed consent and comply with all protocol requirements
Ability to understand and the willingness to sign a written informed consent document; patient must sign the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirements
Subjects provide signed informed consent and confirm that they are able and willing to comply with all protocol requirements. Cohort A Only:
Signed written informed consent and willingness to comply with protocol requirements
Patient has signed the informed consent (ICF) and is able to comply with protocol requirements
Is able to agree to and sign informed consent and to comply with the protocol
Inability to provide informed consent
Inability to understand and sign informed consent
Inability to understand the informed consent document, to give consent voluntarily or to complete the study tasks, especially inability to understand and fulfill the health-related QOL questionnaire;
Inability to understand or give an informed consent
Investigator's opinion of subject's probable noncompliance or inability to understand the trial and/or give adequate informed consent;
Inability to give informed consent
Inability to understand a written informed consent document
Unwilling or inability to give informed consent
Inability to obtain informed consent from patient or surrogate
Inability to provide informed consent
Inability to understand or give an informed consent
Inability to consent
Inability to give informed consent or lacks decision making capacity
Inability to provide consent
Inability to sign informed consent document
Inability to understand or give an informed consent
Inability to obtain informed consent
Inability to give informed consent or assent
Inability to provide informed consent.
Inability to give informed consent
Inability to understand or provide informed consent
Inability to provide informed consent
Inability to give voluntary informed consent or obtain a parent or guardian’s informed consent
Inability to understand or give an informed consent
Inability to understand the investigational nature of the study to provide informed consent
Inability to obtain informed consent because of psychiatric or complicating medical problems
Inability to understand or give an informed consent
Inability to give informed written consent
Inability to give informed written consent
Inability to understand or give an informed consent
Inability to give informed consent
Inability to provide informed consent
Refusal or inability to give informed consent to participate in the trial
Inability to provide informed consent.
Inability to give informed consent
Inability to understand or give an informed consent
Inability to provide informed consent
Inability to give consent
Inability to provide informed consent
Inability to understand or give an informed consent
Inability to give voluntary informed consent or guardian’s informed consent
Inability to provide informed consent
MSC DONOR: inability to provide informed consent
Inability to understand and inability to provide informed consent
Inability to give an informed consent
Inability to provide informed consent
Inability to consent for the procedure
Inability to give informed consent
Inability to consent.
Inability to give informed consent
Inability to provide informed consent
Inability to provide adequate informed consent
Inability to provide informed consent
Inability to provide a fully informed consent.
Inability to provide informed consent
Inability to provide informed consent
Inability to provide informed assent/permission/consent
Inability to provide informed consent
Inability to give informed consent
Inability to provide informed consent; potential participants will be identified by our collaborating physicians
Inability to provide informed consent
Inability to provide informed consent
Inability to provide informed consent
Inability to understand consent procedures
Inability to provide informed consent
Inability to give informed consent
Inability to provide informed consent (and assent, if subject is under the age of 18)
Inability to give informed consent
Inability to provide informed consent on their own behalf
Inability to give written consent
Inability to give informed consent
DONOR: Inability to give informed consent
Inability to perform informed consent due to any medical or psychiatric condition
Inability to provide informed consent
Inability to provide written informed consent
Inability to give informed consent
Inability to provide informed consent
Inability to give informed consent
Inability to provide informed consent
Inability to give informed consent
Inability to give informed consent in person
Inability to give informed consent.
Patients with impaired decision making capacity may participate in the study if a legal authorized representative is available to consent
Patients or their legal representatives must be able to read, understand, provide and sign informed consent to participate in the trial
Able to understand and sign an informed consent (or have a legal representative who is able to do so)
Able to provide informed consent, or have a legal representative able and willing to do so
Provide written informed consent (Subject or legal representative)
Subject or legal representative has ability to read, understand and provide written informed consent for study related procedures
Patients or their legal representative must be able to provide written informed consent;
Informed consent cannot be obtained either from the patient or legal representative
Patients or their legal representative must be able to read, understand and sign an informed consent
Adult patients must be able to understand and sign a written informed consent. For pediatric patients, the parent/legal guardian or representative must be able to understand and sign a written informed consent. Assent, when appropriate, will be obtained according to institutional guidelines.
Patients must be able to understand and be willing to give informed consent; parent or legal representative will be asked to consent for patients younger than 18 years old
Patients or their legal representative must be able to read, understand, and sign a written informed consent
Ability to understand and the willingness to sign a written informed consent document; patients with impaired decision making capacity may be eligible if they have a Legal Authorized representative or caretaker available
Patient or patient’s legal representative must provide written informed consent
Patient or patient’s legal representative able to sign informed consent
Provide written informed consent (or legal representative)
Written informed consent from patient or legal representative
Patient, or the patient’s legal representative, has voluntarily agreed to participate by giving written informed consent
Patient or patient’s legal representative able to provide written informed consent
Either the subject or the subject’s legal representative must be willing and able to provide written informed consent for the trial
Patient or patient’s legal representative, parent(s), or guardian able to provide written informed consent
Patient or patient’s legal representative, parent(s) or guardian able to provide written informed consent
Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent; patients aged 7 to < 18 to provide assent
Patient (if ? 18 years old), or patient's legal representative(s) must have signed informed consent
Patients must be able to give informed consent; parent or legal representative will be asked to consent for patients younger than 18 year old
Subjects or their legal representative must be able to understand and provide written informed consent
All patients or their legal representative (for patients < 18 years old) must sign an Institutional Review Board (IRB) approved informed consent document (cGVHD natural history protocol 04-C-0281 or any National Cancer Institute [NCI] protocol allowing for screening procedures) prior to performing studies to determine patient eligibility; after confirmation of patient eligibility all patients or their legal representative must sign the protocol specific informed consent; for pediatric patients age appropriate assent will be obtained in accordance with NIH guidelines
Written informed consent obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study.
Patients or their legal representative (if the patient is < 18 years old) must be able to read, understand and provide written informed consent to participate in the trial.
Signed, written informed consent by subject or legal representative prior to any trial-specific screening procedure
Subject or an authorized legal representative is willing and able to give prior written informed consent for investigation participation;
Patient or patient’s legal representative able to provide written informed consent
Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent; age 7-18 able to provide assent
Written informed consent obtained from the patient/legal representative;
Written informed consent obtained from the patient/legal representative
Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent
Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent
Able to understand and sign an informed consent (or have a legal representative who is able to do so)
Patient or patient’s legal representative, able to sign informed consent
Patient or patient’s legal representative, parent(s) or guardian able to provide written informed consent for the long-term follow-up gene therapy study 2006-0676
Patients or their legal representative must be able to read, understand and sign an informed consent form (ICF)
Patients or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial
Willingness to sign informed consent by patient or patient’s legal representative
Willing and able to understand and provide written informed consent. For minors or those incapable of providing written informed consent (i.e., incapacitated), understood, written and informed consent must be provided by a parent or legal guardian or representative.
Written patient or parental (or appropriate legal representative) IRB approved informed consent as appropriate.
Subjects, or subject's legal representative, who have provided signed informed consent, and assent when applicable, prior to participation.
Patients or their legal representative must be able to read (or have read to them), understand, and sign a written informed consent (approved by the institutional review board) within 14 days prior to start of treatment.
Patient (or legal representative) is able to understand and provide signed informed consent
Able to understand and sign an informed consent (or have a legal representative who is able to do so)
Written informed consent obtained from subject or subject’s legal representative and ability for subject to comply with requirements of the study
Patient or patient’s legal representative(s) is/are able to provide written informed consent to participate
Patient or legal representative must consent to multi-bio-frequency impedance analysis (MFBIA); the details are to be covered in consent
Adult patients must be able to understand and sign a written informed consent. For minor patients, the parent/legal guardian or representative must be able to understand and sign a written informed consent. Assent, when appropriate, will be obtained according to institutional guidelines.
Patient or parent/legal guardian or representative lacks the full mental capacity to understand and sign a written informed consent.
Written informed consent in accordance with institutional and FDA (food and drug administration) guidelines must be obtained from all subjects (or patients' legal representative).
Able and willing (or have legal representative) to understand the study and provide consent
Subject/legal representative willing and able to provide written informed consent
has the ability to read, understand and provide written informed consent for the initiation of any study related procedures (or legal representative)
Informed consent cannot be obtained either from the patient or legal representative
Subject or his or her legal representative has the ability to read, understand and provide written informed consent for the initiation of any study related procedures
Written informed consent obtained prior any study-specific procedure (patient or parent(s) or legal representative)
DONOR: Donors who are unwilling or unable to sign informed consent (assent when appropriate)
Unable or unwilling to sign the consent form
Unable or unwilling to sign the consent form
Unable to read or understand, and/or unwilling to sign a written consent form which must be obtained prior to treatment.
Patients unable or unwilling to give written, informed consent.
Unable or unwilling to sign the consent form
Unable or unwilling to sign the consent form
Patient is unable or unwilling to sign consent
Unable or unwilling to sign the consent form
Unable or unwilling to sign the consent form
Patients unwilling or unable to sign informed consent document
Patients unwilling or unable to sign informed consent document
Unable or unwilling to give voluntary informed consent/assent
Unable or unwilling to sign the consent form
Patients unwilling or unable to sign informed consent document.
Unable or unwilling to sign the informed consent document
Patients unable or unwilling to give written, informed consent
Patients unwilling or unable to sign informed consent document
Unable or unwilling to sign the consent form
Patients unwilling or unable to sign informed consent document
Unwilling to sign an informed consent
Unwilling to give consent
Unwilling to give consent
Unable or unwilling to sign consent
Unable or unwilling to give written informed consent
Unable/unwilling to sign consent
Unwilling or unable to sign and date the informed consent
Patients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)
Unwilling to give informed consent
Patients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)
Subjects unwilling or unable to given written informed consent
Patients unwilling or unable to sign informed consent
Unwilling to give informed consent
Patients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)
Participants unable or unwilling to give written, informed consent or to undergo MRI imaging
Unable or unwilling to give informed consent
Subjects that are unable or unwilling to give informed consent
unwilling to give informed consent;
Unable or unwilling to give informed consent
Are unwilling to give informed consent
Unable to understand, or unwilling to complete the informed consent process
Subjects who are unable or unwilling to give informed consent
Patients who are unable or unwilling to give informed consent