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.