Signed informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed, dated informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Voluntary signed informed consent (IC)
Signed informed consent
Patients must have given signed, informed consent prior to registration on study
Signed and dated informed consent
Subject has the ability to understand and provide signed informed consent
Procurement: Informed consent explained to, understood by and signed by patient. Patient given copy of informed consent
Informed consent explained to, understood by and signed by patient. Patient given copy of informed consent
Signed, written IRB-approved informed consent
Signed written informed consent
Written and voluntary informed consent understood, signed and dated.
Ability to provide signed Informed Consent Form
Signed written informed consent
Be 18 years of age at the time the informed consent form is signed
Signed informed consent prior to any procedures
Signed informed consent
Provide signed, written 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 and dated written informed consent obtained prior to any study-specific evaluation.
Dated and signed IEC/IRB-approved informed consent.
Signed written informed consent
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
Signed informed consent obtained prior to any screening procedures
The patient must be able to comprehend and have signed the informed consent
Patients must have signed an approved informed consent and authorization permitting the release of personal health information
Signed informed consent
All subjects must have given signed, informed consent prior to registration on study
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed informed consent MUST be obtained from patient or parent/legal guardian (if patient is less than 18 years of age). Consent must be signed prior to any study procedures and study entry
Signed informed consent/assent
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Evidence of a signed informed written consent
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
Patient has signed informed consent
Signed informed consent.
Participant has signed informed consent form (ICF) before any trial related activities and according to local guidelines.
Evidence of a signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the study
PROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient; patient given copy of informed consent
Informed consent explained to, understood by and signed by patient; patient given copy of informed consent
INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
INCLUSION - TREATMENT: Informed consent explained to, understood by, and signed by patient/guardian; patient/guardian given copy of informed consent
Signed and dated written informed consent
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
Signed informed consent according to institutional guidelines must be obtained
Be 18 years old at the time the informed consent form is signed
The participant is capable of understanding and complying with the protocol and has signed the informed consent document
Signed informed consent for the study protocol
INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given a copy of informed consent
INCLUSION - INFUSION: Informed consent explained to, understood and signed by patient/guardian; patient/guardian given a copy of informed consent
Subject has signed and dated informed consent
PROCUREMENT INCLUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
TREATMENT INCLUSION: Informed consent explained to, understood by and signed by patient or guardian; patient or guardian given a copy of the informed consent form
Has provided signed written informed consent
Signed informed consent
• Subject signed inform consent
Written and voluntary informed consent understood, signed and dated.
Signed written informed consent obtained prior to study procedures
In the opinion of the Investigator, the patient is capable of understanding and complying with the protocol and has signed the informed consent document.
Voluntarily signed and dated written informed consent prior to any specific-study procedure.
Signed informed consent
Provision of signed written informed consent
Signed donor and patient/guardian informed consent;
PHASE I: Signed informed consent
PHASE IB: Signed informed consent
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.
Subjects must be able to understand and be willing to sign the written informed consent form; ideally, a signed informed consent form will be appropriately obtained prior to the conduct of any trial-specific procedure; however, if patients have had standard of care assessments performed within the screening period, but before the consent was signed, these will be admissible
ELIGIBILITY CRITERIA AT TIME OF TREATMENT: Informed consent (and assent as applicable) signed by patient/guardian
Signed written informed consent.
PROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Signed informed consent form
Failure to provide signed informed consent
Patient or authorized proxy needs to have signed the informed consent form
Able to provide signed informed consent (or consent provided by legal guardian for pediatric patients, as applicable)
Understand study design, risks, and benefits and have signed informed consent
INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
INCLUSION - TREATMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Patient has signed and dated informed consent
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
The patient must be competent and have signed 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
All patients must have given signed, informed consent prior to registration on study
Signed and dated written informed consent.
Signed written informed consent.
Signed and dated written informed consent.
Signed informed consent
Signed, informed consent
Signed Informed consent form
Signed and dated written informed consent obtained from patient or legal representative.
Eligible and consent signed for imaging with AMT PET under protocol 2011-­053
Evidence of a personally signed informed consent document.
Written informed consent and/or signed assent from patient, parent or guardian.
The patient has not signed a study-specific informed consent for this study.
STUDY ENTRY: Signed Informed Consent Form (ICF).
Signed and dated informed consent
Provide signed written informed consent
Capable of understanding and complying with the protocol requirements and has signed the informed consent document.
Patients must have signed an informed consent document stating that they understand the investigational nature of the proposed treatment
Signed written informed consent
Signed informed consent
Provision of signed and dated informed consent form (ICF).
The participant is capable of understanding and complying with the protocol and has signed the informed consent document
Signed Informed Consent Form.
Signed informed consent according to institutional guidelines must be obtained prior to registration
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 informed consent document and assent when appropriate
Signed written informed consent obtained prior to study procedures
Signed informed consent.
Signed and dated written informed consent
Subjects must be able and willingly give signed informed consent
Signed informed consent
Ability to understand and provide signed informed consent
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed informed consent form (ICF) and comply with the requirements of the study protocol
Have signed informed consent to participate in 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 informed consent
signed written informed consent obtained prior to study procedures
Signed informed consent indicating awareness of the investigational nature of this program
Provision of signed informed consent.
Signed informed consent form (ICF)
Signed informed consent
Participants signed informed consent
Signed informed consent
Have signed written informed consent
Signed informed consent.
Subject has signed and dated informed consent
Provision of signed written informed consent.
Signed 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\r\nprior to their enrollment on the protocol
Capable of understanding and complying with the protocol and has signed the informed consent document
Signed study-specific informed consent
Signed, informed consent
Signed informed consent form (ICF)
Signed informed consent obtained prior to any screening procedures
Signed informed consent;
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
Patient has the ability to understand and provide signed informed consent
Signed informed consent;
Provide signed Informed Consent
Signed consent to long-term follow-up protocol PA17-0483.
Signed informed consent form (ICF)
Signed informed consent form (ICF)
The patient is capable of understanding and complying with the protocol and has signed the informed consent document. A signed informed consent form must be obtained before any study-specific procedures are performed.
Signed and dated written informed consent
Signed written informed consent
>=18 years of age and provided signed written informed consent
Signed informed consent
Signed and dated written informed consent prior to admission to the study
Signed informed consent
Informed consent signed by the subject
Subject has been informed of the study procedures and the treatment and has signed an informed consent form
Signed written informed consent
Signed informed consent
Signed informed consent form in accordance with institutional and federal law policies
Capability to understand and comply with the protocol requirements as and signed informed consent documents
Signed, written informed consent
Signed written informed consent
Subjects must have signed written, informed consent
Capable of giving signed informed consent
Signed informed consent document(s)
Signed informed consent form in accordance with institutional policies prior to the initiation of high-dose therapy
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
Provide signed written informed consent
Signed informed consent on protocol LAB02-188
Have signed an informed consent document
Signed informed consent by patient and/or parents or legal guardian
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, informed consent
Signed informed consent according to institutional guidelines prior to registration.
Informed consent obtained and signed
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 informed consent indicating awareness of the investigational nature of this program
Signed, written informed consent
Signed study-specific consent form
Signed informed consent
Signed informed consent form must be obtained prior to any research procedure
Informed consent reviewed and signed
Signed written informed consent
Signed written informed consent must be obtained prior to any study procedures.
Subjects must have signed written, informed consent
Signed written informed consent
Signed informed consent obtained prior to any screening procedures
Signed consent
Signed informed consent
Have signed the current approved informed consent form
Signed informed consent indicating awareness of the investigational nature of this program
Written informed consent from patient and/or signed assent from patient, parent or guardian
Signed written informed consent form
Ability to understand and provide signed informed consent
Signed informed consent obtained prior to any screening procedures
Subject understood and signed the study specific informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed, written, informed consent
AT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of informed consent
AT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by research subjects/guardian; subject/guardian given copy of informed consent
Patients who have signed informed consent and authorization permitting release of personal health information
Signed informed consent
PROCUREMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copy
TREATMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copy
Signed and dated informed consent form indicating that the patient has been informed of all pertinent aspects of the trial prior to enrollment
Signed informed consent obtained prior to any screening procedures
Patient has signed informed consent and is willing to comply with the protocol
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Patient has the ability to understand and provide signed informed consent
Informed consent form signed by the subject
A signed and dated written informed consent form is obtained from the subject
Informed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.
Ability to understand and provide signed informed consent
Written informed consent and/or signed assent line from patient, parent or guardian
Signed informed consent
Signed informed consent
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
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Provide signed written informed consent
Signed informed consent
Signed and witnessed informed consent and signed authorization for the release of their protected health information
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
Signed informed consent
Written informed consent and/or signed assent line from patient, parent or guardian
Signed informed consent indicating awareness of the scheduling and side effects, as well as testing requirements, of this program
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed informed consent form must be obtained prior to any study procedure
Signed informed consent obtained prior to any screening procedures
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 Form
Ability to understand and provide signed informed consent that fulfills Institutional Review Board’s guidelines
Provide signed written informed consent
Signed informed consent prior to initiation of any study-specific procedure or treatment
Signed informed consent
Signed and dated written informed consent
Patient (if ? 18 years old), or patient's legal representative(s) must have signed informed consent
Signed informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Patient has signed the informed consent document agreeing to the use of the study drug, domperidone
Signed informed consent
Signed and dated written informed consent
Informed consent obtained and signed
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
Signed written informed consent
Signed study-specific informed consent prior to study entry
Patients must have signed an approved informed consent
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Informed consent explained to, understood and signed by patient/guardian; patient/guardian given copy of 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
Signed informed consent
Signed informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Provided signed informed consent.
Signed written pre-registration informed consent document
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 according to institutional guidelines must be obtained
Signed informed consent
Signed informed consent by the patient or legally authorized representative
Written informed consent and/or signed assent line from patient, parent or guardian
The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Informed Consent: Signed by the subject prior to screening.
Consent signed
PART II: The Part 2 consent must be signed
Signed informed consent indicating awareness of the investigational nature of this program
Signed study-specific informed consent form prior to study entry
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Signed informed consent
Signed study-specific consent form prior to registration
Signed study-specific informed consent prior to study entry
Signed informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Signed informed consent indicating awareness of the investigational nature of this program
Provide signed informed consent
Signed informed consent before initiation of any study procedures.
Signed informed consent
Signed and dated informed consent of the patient, available before the start of any specific trial procedure.
Signed informed consent form
Signed informed consent form
Signed informed consent form
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.
Signed written informed consent per institutional and federal regulatory requirements
Patients who have signed informed consent for this long term extension program.
Signed informed consent
Have signed a written informed consent
Subjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed and dated informed consent document.
Signed informed consent
Capable of giving signed informed consent.
Signed written informed consent
Signed consent to long-term follow- up protocol PA17- 0483
Signed informed consent form (ICF).
Signed informed consent on protocol LAB02-188.
Signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the trial prior to randomization
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
ENROLLMENT: Signed informed consent and if applicable pediatric assent.
Signed informed consent form.
Signed informed consent for protocol PA13-0291
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
Informed consent document signed and dated by patient
Patients must provide a signed informed consent form before any trial relates activities are carried out.
Signed written informed consent.
Provide signed informed consent
The patient must signed an informed consent form (ICF).
Signed & dated informed consent prior to Screening evaluations
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed informed consent.
Subjects must provide a signed informed consent before any screening procedures
Signed informed consent form (ICF)
Signed informed consent for the focal laser ablation (FLA) treatment through the 12 month follow up visit
Signed informed consent
Signed informed consent
Signed informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed informed consent
Patients must have signed an approved informed consent and authorization permitting the release of personal health information
Able to provide signed, informed consent
Signed informed consent according to institutional guidelines must be obtained
Signed informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Ability to understand and sign the informed consent; patient must have signed informed consent prior to registration on study
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
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
Patients must have signed an approved informed consent and authorization permitting release of personal health information
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 informed consent
Signed informed consent by the patient or the patient's parent or guardian for patients who are minors
Signed informed consent
Patients must have signed an approved informed consent and authorization permitting the release of personal health information
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed and dated written informed consent to participate in this clinical trial must be obtained prior to any study procedure
Patient is willing to participate in the study and has signed the study informed consent
Signed, written IRB-approved informed consent.
Signed informed consent
Patients must have signed an approved informed consent
Voluntary signed informed consent form (ICF).
Signed study-specific consent form prior to registration
Signed study-specific informed consent
Signed written informed consent
Signed informed consent
A signed informed consent form or minor assent form
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 written informed consent
Signed informed consent prior to any study-related evaluation
Patients must have signed an approved informed consent and authorization permitting release of personal health information
A signed informed consent form or minor assent form
Patients must have been off of chemotherapy for at least 4 weeks prior to day 1 of cycle 1; informed consent can be signed at any time prior to the start of therapy
Signed informed consent form
Signed informed consent
Signed study specific informed consent form;
Signed informed consent prior to any protocol-specific procedures
Signed informed consent
Patient has provided a signed study informed consent form prior to performance of any study related procedure
Signed written informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information.
Signed study-specific consent form prior to registration
Subjects >=18 years of age and provided signed written informed consent.
Signed informed consent
Signed and dated informed consent.
Signed informed consent document
Informed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copy
Informed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copy
Signed informed consent form
Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Participant is able to provide signed informed consent
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Be 18 years old at the time the informed consent is signed
Signed, written informed consent by subject or legal representative prior to any trial-specific screening procedure
Signed informed consent obtained prior to any screening procedures
Signed informed consent
All patients must have given signed, informed consent prior to registration on study
Signed, written informed consent
All subjects must have given signed, informed consent prior to registration on study
Signed informed consent in accordance with federal, local, and institutional guidelines
Patients must have signed an IRB-approved informed consent and authorization permitting release of personal health information.
Signed, written, informed consent
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed written informed consent.
Patients must have signed an approved informed consent and authorization permitting the release of personal health information
Signed informed consent
Signed informed consent
Signed written informed consent
The patient has provided signed informed consent
The patient has signed the study-specific informed consent form
Signed written informed consent for this protocol
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.
Provision of signed and dated, written informed consent
AT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
AT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
Signed informed consent form
Patient has the ability and willingness to provide informed consent and has signed the informed consent document
Signed written informed consent
Signed written informed consent
Informed consent reviewed and signed
Patient has signed a written informed consent.
Provide signed informed consent
Signed, written informed consent.
Signed informed consent form (ICF)
Signed and dated informed consent.
Signed informed consent
Has provided a signed informed consent
Signed written 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
Informed consent and authorization for the release of health information signed by the patient
Signed written informed consent granted
All patients must have given signed, informed consent prior to registration on study
Signed written informed consent
STEP 2 ENROLLMENT AND RANDOMIZATION: the patient has signed informed consent
Signed, written informed consent
Signed informed consent
Willingness and ability to give signed written informed consent
Signed informed consent indicating awareness of the investigational nature of this program
Patients must have signed an approved informed consent
Signed a protocol-specific informed consent
Signed informed consent
Signed study-specific informed consent
Signed informed consent
Signed informed consent from patients and/or their parents or legal guardians
The participant is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Patients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.
Signed informed consent
Has provided signed informed consent for this study.
An approved informed consent must be signed by the patient
Signed informed consent from patients and/or their parents or legal guardians
An approved informed consent and authorization permitting release of personal health information must be signed by patient or guardian
Signed informed consent document
All subjects must have given signed, informed consent prior to registration on study
Signed informed consent by patient and/or parents or legal guardian
Voluntarily signed informed consent.
Signed Informed Consent
Has provided signed informed consent for this study.
Understand and voluntarily signed informed consent
An approved Informed Consent and authorization permitting release of personal health information must be signed by the patient or guardian
Patients must give written informed consent; a copy of the signed informed consent form will be retained in the patient’s chart
Signed written informed consent;
Signed and dated IRB/Approved Informed Consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed informed consent
Has provided signed written informed consent for this study
Signed study-specific informed consent
A signed study specific consent form is required
Signed written informed consent to Study ARQ 197-299
Signed informed consent form (ICF)
Signed written informed consent.
Signed written informed consent.
Patients must have signed an approved informed consent and authorization permitting release of personal information
Signed study-specific informed consent prior to registration
Signed, written informed consent
Signed informed consent document and assent when appropriate
The patient must consent to be in the study and must have signed an approved consent form conforming to institutional guidelines
signed written informed consent
Signed informed consent according to institutional guidelines must be obtained
Patients who have signed an approved Informed Consent
Signed informed consent
Signed informed consent
Have signed an approved informed consent form for the study.
Able and willing to give voluntary, written and signed, informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Provided signed written informed consent
Signed Informed Consent Form (ICF)
Provision of a signed informed consent
Signed informed consent
Provision of a signed informed consent
Signed informed consent
Signed written 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 and dated written informed consent prior to admission to the study
Signed IRB approved Informed Consent Form (ICF).
Signed, approved Informed Consent.
Able to understand and have signed an approved consent form that conforms to federal and institutional guidelines
Signed informed consent
Provide signed written informed consent
Signed informed consent
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Subject has signed and dated informed consent
Provided signed written informed consent
Signed informed consent
Signed informed consent
Signed informed consent
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Procurement consent signed and faxed to Research Coordinator
Signed informed consent
Signed informed consent
Patient must have signed informed consent prior to registration on this study
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
Subjects ? 18 years of age who have signed informed consent
Signed informed consent, which indicates the investigational nature of this study, is required
TREATMENT: Patients must have signed the screening consent
Signed written informed consent
Patients must have signed an approved informed consent
Written and signed informed consent must be obtained
Signed informed consent form (ICF)
Patients must have signed an approved informed consent.
Signed Informed Consent Form
Signed Informed Consent Form
Voluntary signed, written IRB-approved informed consent.
PRE-REGISTRATION INCLUSION CRITERIA: Signed and dated informed consent document for study participation
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
Informed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.
Signed Informed Consent Form
Signed Informed Consent Form
Voluntarily signed and dated written informed consent
Voluntarily signed and dated written informed consent
Signed the informed consent form (ICF)
Evidence of a personally signed and dated written informed consent to participate in the clinical study
Signed informed consent
Patients must have a signed informed consent form prior to enrollment on study
Signed written informed consent.
Subjects, or subject's legal representative, who have provided signed informed consent, and assent when applicable, prior to participation.
Unable to give signed informed consent
Signed informed Consent
Signed Informed Consent Form
Signed informed consent from patient
Informed consent obtained and signed
A signed informed consent document (ICD)
Patient (or legal representative) is able to understand and provide signed informed consent
Signed informed consent
Have signed written informed consent
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, written informed consent.
Signed Informed Consent Form
Signed written informed consent.
Signed written informed consent
Signed informed consent document
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Ability to provide written informed consent. Evidence of a personally signed informed consent.
Signed Informed Consent.
Signed written informed consent
Signed Informed Consent Form
Signed written informed consent
Signed Informed Consent Form
Written informed consent and/or signed assent line from patient, parent or guardian
Signed informed consent
Signed informed consent
Signed informed consent form (ICF)
Signed written informed consent
Signed study-specific informed consent form
Provide signed written informed consent
Signed informed consent.
Signed written informed consent
Signed written informed consent provided
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed informed consent
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 Written Informed Consent
The signed informed consent form
Voluntarily signed and dated written informed consent
Signed informed consent
Signed written informed consent
All patients must have given signed, informed consent prior to registration on study
Signed informed consent
An approved informed consent and authorization permitting release of personal health information must be signed by the patient or guardian
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
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
Informed consent explained to and signed by parent/legal guardian or patient if the patient is >= 18 years
Patient or legal guardian has signed informed consent.
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
Parents or legal guardian signed-written informed consent
Patient and/or legal guardian able to provide signed informed consent
Signed informed consent
Signed and dated written informed consent
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
Patients must have signed an approved informed consent and authorization form permitting the release of personal health information
Signed written informed consent
A personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
Signed informed consent
Written informed consent (IC) for trial participation must be signed and dated by the patient and the investigator prior to enrollment
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Written informed consent signed prior to entry into the study
Signed ICF
Signed and dated Informed Consent Form (by the patient or a legally acceptable representative as per the local regulations).
Signed informed consent form
Capable of giving signed, written informed consent
Voluntary, signed informed consent
All patients will have given signed, informed consent prior to registration
(Patient participation) Signed written informed consent form
Patient must provide signed informed consent.
Provide signed and dated informed consent form
Signed informed consent to the study
Signed informed consent form
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 written informed consent
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Understands study design, risks, and benefits and have signed informed consent
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
Written informed consent form signed and dated by the subject
Patient aged 12-17 years: has signed informed assent and their parent/legal guardian has signed informed consent for study participation
Patient aged 18-25 years: has signed informed consent for study participation
Able to understand and comply with the protocol requirements and has signed the informed consent document.
Signed, written informed consent
Signed informed consent on protocol LAB02-188
Signed informed consent
Signed informed consent`
Signed informed consent
Signed informed consent form from patient
Signed informed consent
Written informed consent and/or signed assent line from patient, parent or guardian
Signed and dated informed consent
Signed a study-specific informed consent prior to study entry
Signed informed consent
Signed informed consent
Signed written informed consent prior to inclusion in the study.
Patients must have signed an approved informed consent and authorization permitting release of personal health information
Signed informed consent.
Signed informed consent
Signed written informed consent by parent(s)/legal guardians of the pediatric patient in compliance with the local laws and regulations. In addition signed children's assent form according to local requirements.
Signed informed consent
Signed informed consent
Informed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of 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
An approved informed consent and authorization permitting release of personal health information must be signed by the patient or guardian
Participants must have a signed written informed consent
Signed and dated written IRB approved informed consent;
Signed informed consent
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 informed consent obtained prior to any screening procedures
Provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed informed consent
Signed informed consent
Signed informed consent
Signed informed consent obtained prior to any screening procedure
Signed study-specific informed consent prior to registration
Signed document of informed consent completed by the parent or legal guardian
Signed informed consent
All subjects must have given signed, informed consent prior to study registration
Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained.
For patients highly suspected to have aGVHD and requiring systemic therapy, informed consent should be signed after biopsy taken to support clinical diagnosis.
For patients at high risk for developing aGVHD, informed consent should be signed prior to transplant.
Provide signed and dated informed consent form
Ability to provide signed informed consent and willingness to comply with protocol requirements
Informed consent must be given and signed
Willingness to signed informed consent
Signed informed consent
Signed, specific informed consent prior to study entry
Signed, informed consent
Signed informed consent
Informed consent or assent signed by study subject or parent/guardian according to institutional guidelines
Signed informed consent indicating awareness of the investigational nature of this study
Signed written informed consent
Patients must have signed informed consent
Signed informed consent form
Provide signed and dated informed consent form.
Subjects must have signed an approved consent form
Have signed informed consent to participate in the study
Signed informed consent
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Signed written informed consent and willingness to comply with protocol requirements
Signed, specific informed consent prior to study entry
Signed, written informed consent
Patient has signed the informed consent (ICF) and is able to comply with protocol requirements
Signed informed consent
Patients with signed informed consent
Signed informed consent
Have signed Informed Consent to participate in the study
Signed consent
Signed consent
Patients who have signed an approved informed consent form
Have signed informed consent to participate in the study
Signed informed consent of the patient
Patients must have signed an informed consent
Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained
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
Received and signed an informed consent form.
Voluntarily signed and dated written informed consent prior to any specific study procedure.
Signed informed consent form
Signed Written Informed Consent
The patient is capable of understanding and complying with the protocol and has signed the informed consent document.
Signed informed consent form.
Subjects must have received and signed an informed consent form.
Voluntarily signed and dated informed consent
Patient has the ability to understand and provide signed informed consent.
Signed informed consent.
Written informed consent will be signed by the patients before the MRI examination
Subjects must have received and signed an informed consent form.
Signed Informed Consent Form
Written Informed Consent not obtained, signed and dated
Signed written informed consent
Before the patient is enrolled, the consent form, including any addenda, must be signed and dated by the patient and the person who explains the study to that patient
Signed informed consent prior to any protocol-specific procedures