Able to provide informed consent prior to initiation of study
Able to provide confirmed consent
Are willing and able to provide signed informed consent.
Patients must be able to provide informed consent.
DONOR: Able to provide informed consent for the donation process per institutional standards.
Willing and able to provide informed consent.
Must be able and willing to participate in all aspects of the study and provide informed consent prior to study participation.
Willing and able to provide informed consent
Participants must be able to provide informed consent for treatment and trial participation
Able to provide informed consent and be willing to participate in study schedule and events.
Willing and able to provide informed consent
Willing and able to provide informed consent
Able to provide informed consent
In the judgment of the consenting professional cognitively able to provide informed consent
Willing and able to provide consent
Willing and able to provide consent
Patient able and willing to provide informed consent.
Willing and able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Able and willing to provide informed consent
Must be able to provide informed consent.
Able to provide informed consent
They must be able to provide informed consent
Able to provide signed, informed consent
Able to provide informed consent
Able to provide informed consent
Patients, or appropriate designee, must be able to provide informed consent
Able and willing to provide consent for required bone marrow biopsies.
Willing and able to provide informed consent
DONOR: Willing and able to provide informed consent
Participant is able to provide signed informed consent
Patients, or appropriate designee, must be able to provide informed consent
Willing and able to provide informed consent
Patient should be able to provide informed consent
COHORT A: The subject must be willing and able to provide informed consent
COHORT B: The subject must be willing and able to provide informed consent
For adult patient, the patient is able to provide informed consent. For pediatric patient, a parent is able to provide informed consent.
Able to provide informed consent and be willing to sign an informed consent form
Willing and able to provide informed consent
Able to provide informed consent and follow protocol requirements.
Patients must be able to provide informed consent
Patient or guardian willing and able to provide informed consent.
Able to provide informed consent for the study
Patients must be able to provide informed consent
Willing and able to provide informed consent
Patients, or appropriate designee, must be able to provide informed consent
At least 18 years of age and willing and able to provide informed consent.
Willing and able to provide informed consent
Able to provide informed consent
Able to provide informed consent, child assent with parental consent or surrogate consent when applicable
Willing and able to provide informed consent;
Patients must be able to provide informed consent
Willing and able to provide informed consent
Age 18 years or older and willing and able to provide informed consent;
Able to provide informed consent
Be able to provide informed consent
Patient/partner is able to provide informed consent
Able to provide informed consent
PATIENT & PARTNER: Able to provide informed consent
Able to provide informed consent
Must be able to provide own consent
PATIENTS AND CAREGIVERS: Able to provide informed consent.
Able to provide informed consent
Phase I: Able to provide informed consent
Phase II: Able to provide informed consent
Able to provide informed consent
Cannot provide meaningful informed consent
In the judgment of the consenting professional cognitively able to provide informed consent
In the judgment of the consenting professional cognitively able to provide informed consent
Able and willing to provide informed consent
PATIENTS AND PARTNERS: Able to provide consent
Adults who are able to provide informed consent
Willing and able to provide informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Subject is able to provide informed consent
Able to provide informed consent
Capable and willing to provide Informed consent
FCGs: Able to provide informed consent
PATIENTS: Not able to provide informed consent
Able to provide informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Patients must be able to provide informed consent
Able to provide informed consent
PHASE I: Able to provide meaningful informed consent
PHASE II: Able to provide meaningful informed consent
Willing and able to provide signed, informed consent
Subjects able to provide informed consent
Able and willing to provide consent (both)
PATIENT: Be able and willing to provide informed consent
Able and willing to provide informed consent
Willing and able to provide, signed informed consent
Able to provide informed consent
The subject must be willing and able to provide informed consent
Able to provide informed consent
Able to provide informed consent
Cognitively able and willing to provide consent
Able to provide informed consent in English
Subjects willing and able to provide consent to participating in the study
Able to provide verbal consent
Able to provide informed consent
Able to provide informed consent to participate in the study
Able to provide informed consent
Able to provide informed consent
Patients who are willing and capable to provide informed consent
Capable and willing to provide informed consent
The patient is willing and able to provide informed consent.
Able to provide legally effective informed consent
Are able to provide informed consent
Patients must be capable and willing to provide informed consent
Willingness to participate in the study and able to provide informed consent
Patients must be able to provide informed consent
Patients must be capable and willing to provide informed consent.
Able to provide informed consent and follow the study guidelines
Patient able and willing to provide informed consent
Able to provide informed consent
Able to provide informed consent
Refusal to provide informed consent
HCC PATIENTS: Patient is willing to provide informed consent
Are able to provide informed consent
Able to provide informed consent
The patient must be willing and able to provide informed consent
Willing and able to provide informed consent
Are able to provide informed consent
Be willing and able to provide informed consent
NORMAL VOLUNTEERS: Be willing and able to provide informed consent
Able to provide informed consent
Able to provide informed consent
Able to provide informed consent (Pre-pilot phase, Arms 1-4, PCS study)
Able to provide informed consent to participate in the study
Must be able to provide informed consent
Willing and able to provide informed consent and fill out demographic, disease, and pain assessment questionnaires