Patients must be informed of the experimental nature of the study and its potential risks, and must sign an Institutional Review Board (IRB)-approved written informed consent form indicating such an understanding
Signed written Institutional Review Board (IRB)-approved informed consent document
Able to and provides Institutional Review Board (IRB) approved study specific written informed consent
Eligible and consent to the Institutional Review Board (IRB) 13-0002 registry trial protocol
Informed consent: All patients or their legal guardians (if the patient is <18 years of age) must sign an Ethics or institutional Review Board approved consent form indicating their awareness of the investigational nature and the risks of this study. When appropriate, younger patients will be included in all discussions in order to obtain assent.
Patients must sign Institutional Review Board (IRB) approved study specific informed consent
Ability to understand and provide signed informed consent that fulfills institutional review board (IRB)’s guidelines
Is willing to voluntarily sign and date an informed consent form that is approved by an institutional review board before the conduct of any study procedure
All subjects must have the ability to understand and the willingness to sign a written informed consent; signed informed consent form approved by the Institutional Review Board (IRB) is required; the patient, family member, and transplant staff physician (physician, nurse, and social worker) meet at least once prior to starting the transplant procedure; during this meeting, all pertinent information with respect to risks and benefits to the donor and recipient will be presented; alternative treatment modalities will be discussed
Patients must be informed of the experimental nature of the study and its potential risks, and must sign an Institutional Review Board (IRB)-approved written informed consent form indicating such an understanding
Signed informed consent approved by the Institutional Review Board
Willing to sign consent onto the Mayo Clinic Radiotherapy Patient Outcomes Registry and Biobanking study, Institutional Review Board (IRB) number 15-000136 (blood draw optional)
have read, understood and signed the informed consent form (ICF) approved by the Institutional Review Board (IRB);
Patients must also provide written consent for biospecimens collection on Institutional Review Board (IRB) 08-000980
Written informed consent to participate in the study according to the investigational review board (IRB)
Must be fully informed regarding their illness and the investigational nature of the study protocol, and must sign an Institutional Review Board (IRB) approved Informed Consent Form (ICF).
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator’s Institutional Review Board (IRB)/Ethics Committee
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator’s Institutional Review Board (IRB)/Ethics Committee
Written consent on an Institutional Review Board-approved informed consent form prior to any study-specific evaluation
All subjects must have the ability to understand and the willingness to sign a written informed consent that has been approved by the City of Hope Institutional Review Board (COH IRB); the patient, a family member and transplant staff physician (physician, nurse, social worker) will meet at least once prior to the subject signing consent; during this meeting all pertinent information with respect to risks and benefits to donor and recipient will be presented; alternative treatment modalities will be discussed; the risks are explained in detail in the enclosed consent form
Ability to understand the purposes and risks of the study and has signed a written consent form approved by the investigator’s Institutional Review Board (IRB)/ethics committee
Study-specific informed consent approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan indicating that they are aware of the investigational nature of the treatment and the potential risks must be signed by the patient
Ability to understand and provide signed informed consent that fulfills Institutional Review Board (IRB) guidelines
Signed informed consent approved by the Institutional Review Board
Patient is unwilling or unable to sign and date the Institutional Review Board (IRB) approved informed consent
Signed informed consent approved by the Institutional Review Board prior to patient entry
Patients must be informed of the experimental nature of the study and its potential risks, and must sign an Institutional Review Board (IRB)-approved written informed consent form indicating such an understanding
Signed informed consent approved by the Institutional Review Board prior to patient entry
Patients must voluntarily provide written Institutional Review Board (IRB)-approved informed consent
Patients will sign an Institutional Review Board (IRB)-approved informed consent form prior to any study-related procedures
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator’s Institutional Review Board (IRB)/Ethics Committee
Signed informed consent approved by the Institutional Review Board
Relapsed/refractory MCL: Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Understanding and voluntarily signing an Institutional Review Board (IRB)-approved informed consent form
Co-enrollment on Institutional Review Board (IRB) #98117, entitled Molecular Pathogenesis of Therapy-Related Leukemia, Dr. Armenian, principal investigator
Written informed consent and/or Consent waiver by institutional review board (IRB)
Institutional Review Board (IRB)-approved informed consent obtained and signed
Subjects must give institutional review board (IRB)-approved study-specific informed consent
Patients must have signed informed consent both for this study and the research use of data in the UAB bone marrow transplantation (BMT) program's Institutional Review Board (IRB) registered clinical database
FOR TISSUE COLLECTION TO ESTABLISH PDX (PART 1): Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form.
Signed, written Institutional Review Board (IRB)-approved informed consent form (ICF)
All patients or their legal guardians (if the patient is < 18 years old) must sign an Institutional Review Board (IRB)-approved document of informed consent to demonstrate their understanding of the investigational nature and the risks of this study before any protocol-related studies are performed; when appropriate, pediatric subjects will be included in all discussions
Patients must understand and be willing to sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Medical Center indicating that they are aware of the investigational aspects of the treatment and the potential risks
DONOR: The donor or legal guardian greater than 18 years of age, capable of signing an Institutional Review Board (IRB)-approved consent form
Willing to provide consent to Institutional Review Board (IRB) number (#) 521-93 and provide research tissue and blood specimens
All patients must be informed about the study and have signed a current Institutional Review Board (IRB) approved informed consent
Understanding and voluntary signing an institutional review board (IRB)-approved informed consent form
Patients must be informed of the experimental nature of the study and its potential risks and must sign an Institutional Review Board (IRB)-approved written informed consent form indicating such an understanding
Patients must exercise informed voluntary consent and sign a consent form approved by the University of Minnesota Institutional Review Board (IRB): Human Subjects Committee
Ability to understand and provide signed informed consent that fulfills Institutional Review Board (IRB)’s guidelines
Signed informed consent approved by the Institutional Review Board
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's Institutional Review Board (IRB)/Ethics Committee
Written informed consent to participate in the study according to the Investigational Review Board (IRB)
Signed, Institutional Review Board (IRB)-approved written informed consent
Participants must sign the most current institutional review board (IRB)-approved study informed consent form (ICF)
Signed informed consent approved by the Institutional Review Board prior to patient entry
Signed informed consent approved by the Institutional Review Board prior to patient entry
Patients must be informed of the experimental nature of the study and its potential risks, and must sign an Institutional Review Board (IRB)-approved written informed consent form indicating such an understanding
Signed an Institutional Review Board (IRB)-approved informed consent document for this protocol
Signed an institutional review board (IRB)-approved informed consent document for this protocol
Optional participation in the microdose imaging trial, Institutional Review Board (IRB)#10-139
Patients must be informed of the experimental nature of the study and its potential risks and must sign an institutional review board (IRB)-approved written informed consent form indicating such an understanding
E 14. Absence of signed and dated Institutional Review Board (IRB)-approved participant informed consent form prior to enrollment into the study.
Signed, Institutional Review Board (IRB)-approved written informed consent
Signed, Institutional Review Board (IRB)-approved written informed consent
Ability to understand and provide signed informed consent approved by the Institutional Review Board prior to any study-related activities and within 30 days of first study dose
Patients must agree to randomization as documented by signing the Institutional Review Board (IRB) approved consent form
Patients or a legal guardian will sign an informed consent form approved by the Institutional Review Board (IRB) and obtained by the principal or a co-investigator before patient entry; minors will provide assent
Patients must sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Medical Center indicating that they are aware of the investigational aspects of the treatment and the potential risks
Signed and dated institutional review board (IRB)-approved informed consent before any protocol-specific screening procedures are performed.
Signed and dated Institutional Review Board (IRB)-approved consent form
Provide written informed consent for study participation, approved by the appropriate institutional review board (IRB), and be willing and able to cooperate with all aspects of the protocol;
Prospective study participants must be informed of the investigational nature of the study and must have signed an Institutional Review Board (IRB)-approved informed consent form in accordance with institutional and federal guidelines
Understanding and voluntary signing an Institutional Review Board (IRB)-approved informed consent form
Fully informed about their illness and the investigational nature of the study protocol and must sign and date an Institutional Review Board-approved Informed Consent Form
Absence of signed and dated Institutional Review Board-approved patient informed consent from prior to enrollment in the study
Competent to sign and date an Institutional Review Board approved informed consent form
Patients must have signed the current Institutional Review Board (IRB) approved informed consent prior to registration (see Informed Consent).
Institutional Review Board (IRB) approved, signed written informed consent
Enrollment within 6 weeks of tumor board review
Signed, Institutional Review Board (IRB)-approved written informed consent
Institutional review board (IRB) approved signed written informed consent
Signed informed consent approved by the Duke Institutional Review Board
Signed informed consent approved by the Institutional Review Board prior to patient entry
Institutional Review Board (IRB) approved, signed written informed consent
Institutional Review Board (IRB) approved signed written informed consent
Signed Institutional Review Board (IRB) approved written informed consent
All patients must sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Pennsylvania
Signed an Institutional Review Board (IRB)-approved informed consent
Signed written informed consent approved by the Institutional Review Board obtained prior to study entry
All subjects must have the ability to understand and the willingness to sign a written informed consent that has been approved by the City of Hope (COH) Institutional Review Board (IRB); the patient, a family member and transplant staff physician (physician, nurse, and social worker) will meet at least once prior to the subject signing consent; during this meeting all pertinent information with respect to risks and benefits to donor and recipient will be presented; alternative treatment modalities will be discussed; the risks are explained in detail in the enclosed consent form
The study has been explained to the patient/volunteer and the subject has signed the Institutional Review Board (IRB)-approved informed consent form prior to optical measurements
Able to and provides Institutional Review Board (IRB) approved study specific written informed consent
Are able to give written informed consent in a manner approved by the Institutional Review Board and comply with the requirements of the study.
Patient must consent to be in the study and must have signed and dated an Institutional Review Board (IRB) approved consent form conforming to federal and institutional guidelines
TNBC patients who are previously untreated and enrolled in the prospective Institutional Review Board (IRB) approved clinical trial: 2014-0185
Consent: patients must be able to give written, informed consent as approved by the local Institutional Review Board (IRB)
Have read and signed the Institutional Review Board (IRB)-approved informed consent form for participating in the study
Will sign the Institutional Review Board (IRB)-approved consent form
Women must be enrolled in Atlanta Women’s human immunodeficiency virus (HIV) Interagency Study (WIHS) (institutional review board [IRB] # 00062469)
PATIENT: Have read and signed the Institutional Review Board (IRB)-approved informed consent form for participating in the study
Patients must understand and be willing to sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Medical Center indicating that they are aware of the investigational aspects of the treatment and the potential risks
All patients or their legal guardians (if the patients is < 18 years old) must sign an Institutional Review Board (IRB)-approved document of informed consent to demonstrate their understanding of the investigational nature and the risks of this study before any protocol-related studies are performed; when appropriate, pediatric subjects will be included in all discussions
The study population may include illiterate persons and University Hospital (UH)/Case employees if they meet other inclusion criteria; the consent process for these potential participants will be conducted according to Institutional Review Board (IRB) guidelines
Written informed consent will be signed by the patients before the MRI based on the guidelines approved by the Ohio State University Institutional Review board
Signed, Institutional Review Board (IRB)-approved written informed consent
Institutional Review Board (IRB) written informed consent obtained and signed
Subjects must have signed Institutional Review Board (IRB)-approved informed consent documentation
Subjects must have signed an institutional review board (IRB)-approved informed consent document
Subjects (or their parent or legal guardian) must have signed Institutional Review Board (IRB)-approved assent/informed consent documentation
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's Institutional Review Board (IRB)/Ethics Committee
Be Institutional Review Board (IRB)-approved and open to accrual at USC Norris
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an institutional review board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved, written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an institutional review board (IRB)-approved written informed consent document (legally authorized representative permitted)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an institutional review board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document (either directly or via a legally authorized representative)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable).
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an institutional review board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable).
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Patient (or legally authorized representative if applicable) must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (legally authorized representative is allowed)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an institutional review board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and be willing to sign an Institutional Review Board (IRB) approved written informed consent document (or legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document (legally authorized representative permitted)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Patient (or legally authorized representative if applicable) must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Patient (or legally authorized representative if applicable) must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB), approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Able to understand and willing to sign an institutional review board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document (either directly or via a legally authorized representative)
Patient (or legally authorized representative if applicable) must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Legally authorized representative/guardian must be able to understand and willing to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document (or that of legally authorized representative, if applicable)
Signed informed consent
Signed informed consent
Patients must have given signed, informed consent prior to registration on study
Signed informed consent prior to any procedures
Signed informed consent
Patients must have signed an approved informed consent
Ability to understand and the willingness to sign a written informed consent document; NOTE: consent documents can be signed up to 30 days prior to registration; if > 30 days has elapsed since patient signed the consent document, s/he must re-consent (new signature) before proceeding to register onto study
Signed informed consent
All subjects must have given signed, informed consent prior to registration on study
Signed informed consent/assent
Patient has signed informed consent
Signed informed consent.
Signed informed consent for the study protocol
Signed informed consent
• Subject signed inform consent
Signed informed consent
PHASE I: Signed informed consent
PHASE IB: Signed informed consent
Failure to provide signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed informed consent
Signed, informed consent
Evidence of a personally signed informed consent document.
Signed informed consent
Signed informed consent document and assent when appropriate
Signed informed consent.
Subjects must be able and willingly give signed informed consent
Signed informed consent
Have signed informed consent to participate in the study
Signed informed consent
Signed informed consent
Participants signed informed consent
Signed informed consent
Signed informed consent.
Signed informed consent
Signed, informed consent
Signed informed consent;
Signed informed consent;
Provide signed Informed Consent
Signed informed consent
Signed informed consent
Informed consent signed by the subject
Signed informed consent
Signed informed consent document(s)
Signed informed consent on protocol LAB02-188
Have signed an informed consent document
Signed, informed consent
Informed consent obtained and signed
Signed informed consent
Informed consent reviewed and signed
Signed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Patients must have signed an approved informed consent
Signed informed consent document(s)
Signed informed consent
Signed informed consent
Signed informed consent
Informed consent obtained and signed
Patients must have signed an approved informed consent
Signed informed consent
Signed informed consent
Provided signed informed consent.
Signed written informed consent\r\n* The signed informed consent\r\n* The benefits/risks of the induction chemotherapy regimen will be reviewed, and a second consent may be necessary if the regimen will be administered according to a separate protocol
Signed informed consent
Informed Consent: Signed by the subject prior to screening.
Consent signed
PART II: The Part 2 consent must be signed
Signed informed consent
Signed informed consent
Provide signed informed consent
Signed informed consent
Signed informed consent
Patients must have voluntarily signed an informed consent in accordance with institutional policies.
All patients must have given a signed, informed consent prior to enrollment on study
Signed informed consent.
Patients who have signed informed consent for this long term extension program.
Signed informed consent
Signed informed consent
Signed informed consent on protocol LAB02-188.
Signed informed consent for protocol PA13-0291
Provide signed informed consent
Signed informed consent.
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Ability to understand and sign the informed consent; patient must have signed informed consent prior to registration on study
Signed and informed consent to participant in this study
Signed informed consent to participate in this study
Patients must have signed an approved informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Patient is willing to participate in the study and has signed the study informed consent
Signed informed consent
Patients must have signed an approved informed consent
Signed informed consent
Signed informed consent prior to any study-related evaluation
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent document
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
All subjects must have given signed, informed consent prior to registration on study
Signed informed consent
Signed informed consent
The patient has provided signed informed consent
Informed consent reviewed and signed
Provide signed informed consent
Signed informed consent
Has provided a signed informed consent
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed Informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed informed consent
Patients must have signed an approved informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Has provided signed informed consent for this study.
An approved informed consent must be signed by the patient
Signed informed consent document
All subjects must have given signed, informed consent prior to registration on study
Voluntarily signed informed consent.
Signed Informed Consent
Has provided signed informed consent for this study.
Signed informed consent
Signed informed consent document and assent when appropriate
Patients who have signed an approved Informed Consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent prior to the start of systemic therapy; in the event of enrollment of a minor patient, an attempt to obtain assent from the patient must be documented, and parental consent must be signed
Signed, approved Informed Consent.
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Patient must have signed informed consent prior to registration on this study
Subjects ? 18 years of age who have signed informed consent
TREATMENT: Patients must have signed the screening consent
Patients must have signed an approved informed consent
Patients must have signed an approved informed consent.
Signed informed consent
Unable to give signed informed consent
Signed informed Consent
Signed informed consent from patient
Informed consent obtained and signed
A signed informed consent document (ICD)
Signed informed consent
Signed informed consent document
Signed Informed Consent.
Signed informed consent
Signed informed consent
Signed informed consent.
Signed informed consent
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed informed consent
The subject has the capability of understanding the informed consent document and has signed the informed consent document
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
All patients will have given signed, informed consent prior to registration
Patient must provide signed informed consent.
Signed informed consent to the study
Have read and signed study informed consent document (ICF)
Signed informed consent
All participants must have given signed, informed consent prior to registration in study
Signed informed consent
Has signed consent within 6 months of diagnosis date
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent on protocol LAB02-188
Signed informed consent
Signed informed consent`
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent.
Signed informed consent
Signed informed consent
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed informed consent
Signed the 2 year extension study informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent obtained prior to any screening procedure
Signed informed consent
All subjects must have given signed, informed consent prior to study registration
Informed consent must be given and signed
Willingness to signed informed consent
Signed informed consent
Signed, informed consent
Signed informed consent
Patients must have signed informed consent
Have signed informed consent to participate in the study
Signed informed consent
Signed informed consent
Patients with signed informed consent
Signed informed consent
Have signed Informed Consent to participate in the study
Signed consent
Signed consent
Have signed informed consent to participate in the study
Signed informed consent of the patient
Patients must have signed an informed consent
Participants must be willing to participate and provide signed informed consent
give signed informed consent prior to the initiation of therapy
Signed informed consent for patient’s participating in the paper based survey
Signed informed consent.
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document and follow study procedures including willingness to undergo study biopsies
Ability to understand and willingness to sign Institutional Review Board (IRB)-approved informed consent
Ability to understand and the willingness to sign a written informed consent document that is approved by the local institutional review board
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an institutional review board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Patients must sign the Institutional Review Board (IRB)-approved informed consent document for this trial
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Sign an Institutional Review Board (IRB)-approved informed consent document
All patients must sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved written informed consent document
All patients must sign an Institutional Review Board (IRB)-approved informed consent document
All patients must sign an institutional review board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign a written Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Informed consent: all subjects must have the ability to understand and the willingness to sign an Institutional Review Board (IRB) approved consent form
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Understand and voluntarily sign an institutional review board (IRB)-approved informed consent form
Ability to understand and the willingness to sign a written informed consent document that is approved by an institutional review board
Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Sign an institutional review board (IRB)-approved informed consent document
Ability to understand and the willingness to sign a written informed-consent document that is approved by the local institutional review board
Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Understand and voluntarily sign an Institutional Review Board (IRB) approved informed consent form
Sign an Institutional Review Board (IRB)-approved informed consent document
Sign an Institutional Review Board (IRB)-approved informed consent document
Sign an Institutional Review Board (IRB)-approved informed consent document
Ability to read, understand, and sign a written informed consent approved by each Institutional Review Board (IRB); alternatively, patients with legal guardians who can read, understand, and sign written informed consent may also enroll
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign the Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an institutional review board (IRB)-approved informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and willingness to sign an Institutional Review Board (IRB) approved written informed consent document
Ability to understand and the willingness to sign a written informed consent document that is approved by the local institutional review board
Patients must sign an Institutional Review Board (IRB)-approved informed consent document
Ability to understand and the willingness to sign an institutional review board (IRB)-approved informed consent document
Patients must sign an institutional review board (IRB)-approved informed consent document
Subject must be able to give written Institutional Review Board (IRB) approved informed consent and be able to follow protocol requirements
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Patients must be able to understand and agree to sign an institutional review board (IRB)-approved informed consent form
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Individuals able to understand and willing to sign an Institutional Review Board (IRB)-approved informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an institutional review board (IRB) approved written informed consent document
Be able to give written Institutional Review Board (IRB) approved informed consent and be able to follow protocol requirements
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
DONOR: Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Patients must be able to understand and agree to sign an Institutional Review Board (IRB)-approved informed consent form
Understand and sign, written Institutional Review Board (IRB)-approved informed consent form, and be willing to comply with all study procedures
Patients must be able to understand and agree to sign an Institutional Review Board (IRB)-approved informed consent form
Able to understand and willing to sign an institutional review board (IRB) approved written informed consent document
Able to understand and willing to sign an institutional review board (IRB)-approved written informed consent document
Able to understand and willing to sign Institutional Review Board (IRB)-approved written informed consent document
Able to understand and sign the Institutional Review Board (IRB)-approved informed consent document for this trial
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved informed consent document
Patient must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Patient must be able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Willing to sign an Institutional Review Board (IRB)-approved informed consent document and adhere to the protocol
Able to understand and willing to sign an institutional review board (IRB)-approved informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Patients must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Patients must sign an Institutional Review Board (IRB) approved informed consent form for this purpose indicating that they are aware of the investigational aspects of the treatment and the potential risks; they also must be able to understand and the willing to sign a written informed consent
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign Institutional Review Board (IRB) approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and sign an Institutional Review Board (IRB)-approved informed consent form
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able and willing to sign an Institutional Review Board (IRB)-approved written informed consent
Patient must be able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Willing and able to understand and sign informed consent form approved by the institutional review board (IRB)
Must be able and willing to sign an informed consent approved by the Institutional Review Board (IRB)
Must be able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent\r\ndocument
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Participant must be able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
Patient: Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document
Patient understands the study regimen, its requirements, risks and discomforts and is able and willing to sign the informed consent form; voluntary signed and dated Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines must be obtained before the performance of any protocol related procedures that are not part of normal patient care; subjects must be competent to report adverse events (AEs), understand the drug dosing schedule and use of medications to control AEs
Patients must have signed and dated an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent form (ICF) in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal patient care
Able to understand and willingness to provide informed consent, and the willingness to comply with the requirements of the protocol\r\n* Subjects must have signed and dated an Institutional Review Board (IRB)/Independent Ethics Committees (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines and before the performance of any protocol related procedures that are not part of standard of care
Participants must be able to give self-consent and then sign and date an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent in accordance with local regulatory and institutional guidelines; this consent must be obtained before the performance of any protocol-related procedures that are not considered part of normal participant care
Subjects must have signed and dated an Institutional Review Board/Independent Ethics Committee (IRB/IEC) approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care.
Subjects must have signed and dated an Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Subjects must have signed and dated an Institutional Review Board/Independent Ethics Committee (IRB/IEC) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Subjects must have signed and dated an Institutional Review Board (IRB)-approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol-related procedures that are not part of normal subject care
Voluntary signed and dated Institutional Review Board (IRB) approved informed consent form in accordance with regulatory and institutional guidelines
Voluntary signed and dated Institutional Review Board (IRB) approved informed consent form in accordance with regulatory and institutional guidelines
Patients must have signed and dated an Institutional Review Board (IRB) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Patient understands the study regimen, its requirements, risks and discomforts and is able and willing to sign the informed consent form; voluntary signed and dated Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines must be obtained before the performance of any protocol related procedures that are not part of normal patient care
Participants must have signed and dated an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol-related procedures that are not part of normal patient care
Subjects who voluntarily signed and dated Institutional Review Board approved informed consent form in accordance with regulatory and institutional guidelines. Hepatocellular Carcinoma Inclusion Criteria:
Subjects must have signed and dated an Institutional Review Board (IRB)/Institutional Ethics Committee (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Signed written informed consent\r\n* Subjects must have signed and dated an Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care\r\n* Subjects must be willing and able to comply with scheduled visits, treatment schedule, and laboratory testing
Subjects must have signed and dated an Institutional Review Board/Independent Ethics Committee (IBR/IEC) approved written informed consent form in accordance with regulatory and institutional guidelines
Patients must have signed and dated an Institutional Review Board/Independent Ethics Committee -approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol-related procedures that are not part of normal patient care
Subjects must have signed and dated an institutional review board (IRB) approved written informed consent in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Signed, written IRB-approved informed consent
Signed written informed consent
Signed written informed consent
Provide signed, written informed consent.
Signed written informed consent
Evidence of a signed informed written consent
Has provided signed written informed consent
Signed written informed consent.
Signed written informed consent.
Provide signed written informed consent
Signed written informed consent
Have signed written informed consent
Signed written informed consent
>=18 years of age and provided signed written informed consent
Signed written informed consent
Signed, written informed consent
Signed written informed consent
Subjects must have signed written, informed consent
Provide signed written informed consent
Signed, written informed consent
Signed written informed consent
Subjects must have signed written, informed consent
Signed written informed consent
Signed, written, informed consent
Provide signed written informed consent
Provide signed written informed consent
Signed written informed consent
Signed written pre-registration informed consent document
Have signed a written informed consent
Signed written informed consent
Signed written informed consent.
Signed, written IRB-approved informed consent.
Signed written informed consent
Signed written informed consent
Signed written informed consent
Subjects >=18 years of age and provided signed written informed consent.
Signed, written informed consent
Signed, written, informed consent
Signed written informed consent.
Signed written informed consent
Signed written informed consent for this protocol
Signed written informed consent
Signed written informed consent
Patient has signed a written informed consent.
Signed, written informed consent.
Signed written informed consent
Signed written informed consent granted
Signed written informed consent
Signed, written informed consent
Willingness and ability to give signed written informed consent
Signed written informed consent;
Has provided signed written informed consent for this study
Signed written informed consent to Study ARQ 197-299
Signed written informed consent.
Signed written informed consent.
Signed, written informed consent
signed written informed consent
Provided signed written informed consent
Signed written informed consent
Provide signed written informed consent
Provided signed written informed consent
Signed written informed consent
Written and signed informed consent must be obtained
Signed written informed consent.
Have signed written informed consent
Signed, written informed consent.
Signed written informed consent.
Signed written informed consent
Signed written informed consent
Signed written informed consent
Signed written informed consent
Provide signed written informed consent
Signed written informed consent
Signed written informed consent provided
Signed Written Informed Consent
Signed written informed consent
Signed written informed consent
Written informed consent signed prior to entry into the study
Signed written informed consent
Signed, written informed consent
Signed written informed consent prior to inclusion in the study.
Participants must have a signed written informed consent
Signed written informed consent
Signed, written informed consent
Signed Written Informed Consent
Written informed consent will be signed by the patients before the MRI examination
Signed written informed consent
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must have consented to participate and, prior to beginning specific study procedures, must have signed and dated an appropriate IRB-approved consent form that conforms to federal and institutional guidelines for study treatment and for submission of tumor samples as required by NSABP B-59/GBG 96-GeparDouze for baseline correlative science studies.
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Patients must consent to be in the study and must have signed and dated an approved consent form, which conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Patients must be able to provide informed consent and be willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Patients must be able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
STUDY TREATMENT: Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Ability to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
The patient or, if applicable, her legally authorized representative must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
COHORT II: The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Patients must consent to be in the study and sign an approved consent form conforming with institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
The patient must consent to be in the study and must have signed an approved consent form conforming to institutional guidelines
Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
Able to understand and have signed an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
The patient must have signed and dated an Institutional Review Board (IRB)-approved consent form that conforms to federal and institutional guidelines