The subject is willing and able to abide by the protocol
Willing to comply with clinical trial instructions and requirements, including mandatory biopsies
Patients willing to comply with study requirements
Be willing to comply with clinical trial instructions and requirements.
Be willing to comply with clinical trial instructions and requirements, including mandatory biopsies.
Patient willing to conform to the study requirements
Willing and able to participate in the trial and comply with all trial requirements.
Subject is able to understand and willing to comply with protocol requirements and instructions
Patients must be able to comply with all protocol requirements
Willing and able to comply with study requirements for follow-up
Are willing and able to comply with the protocol requirements
Subject is able to understand and comply with protocol requirements and instructions
Able to comply with the study protocol, in the investigators judgment
Be willing to comply with treatment protocol
Able to comply with study protocol, in the investigators judgment
Patients willing to comply with the clinical trial protocol
Subject is able to understand and willing to comply with protocol requirements and instructions
Be willing to comply with treatment protocol
Be willing to participate in the study and comply with all study requirements
Participants must be able to understand and willing to comply with protocol requirements as assessed by the investigator.
Subject is, in the investigators opinion, willing and able to comply with the protocol requirements
DONOR: Able and willing to comply with the requirements of the protocol
Be willing and able to comply with this protocol
Subject is able and willing to comply with the requirements of the protocol.
Willing and able to comply with all study requirements, including treatment, and attending required assessments
The subject is able to understand and comply with protocol requirements, timetables, instructions and protocol-stated restrictions
Participant must be willing and comply with the requirements of the protocol
Patients willing and able to comply with the study protocol for the duration of the study
Able and willing to comply with testing and treatment as outlined in this protocol
Patients must be willing and able to give written informed consent prior to any protocol-specific procedures being performed and comply with the protocol requirements for the duration of the study.
Subject is willing and able to comply with the protocol for the duration of the study
Willing and able to comply with all study requirements, including treatment, timing and nature of required assessments
Patients must agree/be able to comply with all protocol specific requirements
Able to comply with the study protocol, in the investigators judgment
Not willing to follow protocol requirements or to give informed consent
Willing and able to comply with all study requirements, including treatment and required assessments
Patients must meet the following criteria on screening examination to be eligible to participate in the study; all laboratory assessments should be performed within  days of initiation of protocol therapy unless otherwise specified; subject is, in the investigators opinion, willing and able to comply with the protocol requirements
Patient is willing and able to participate in the study and comply with all study requirements.
Individuals not willing to comply with the procedural requirements of this protocol
Individuals not willing to comply with the procedural requirements of this protocol
Patients must be willing to comply with effective Antiretroviral Therapy.
Be willing to comply with the protocol.
Willing and able to participate in the trial and comply with all trial requirements.
Participant is willing and able to comply with the requirements of the protocol
Willing and able to participate in the trial and comply with all trial requirements
Participant is willing and able to comply with the requirements of the protocol
Subject is willing and able to comply with the requirements of the protocol.
Subject is able to understand and comply with protocol requirements and instructions
Willing and able to participate in the trial and comply with all trial requirements.
Be willing and able to comply with the protocol
The patient must be willing and able to comply with study requirements, remain at the clinic, and be willing and able to return to the clinic for the follow-up evaluation as specified in this protocol during the study period.
Able and willing to comply with protocol requirements, in the opinion of the investigator.
Is the subject willing and able to abide by the protocol?
Must be able to understand and comply with protocol requirements and instructions
Patients must be informed of the Celgene Risk Management Program and mandatory registration as well as be willing and able to comply with its requirements
Subject is able and willing to comply with the requirements of the protocol.
Participant is willing and able to comply with the requirements of the protocol
In order to obtain lenalidomide, patients must be registered into the mandatory RevlimidREMS program during the maintenance phase of therapy, and be willing and able to comply with the requirements of RevlimidREMS
Able to understand and comply with the requirements of the protocol
Willing and able to comply with the protocol guidelines for the duration of the study
Willing and able to meet all study requirements
Willing and able to do all study requirements
Subject is willing and able to comply with the follow-up regimen
Willing and able to meet all study requirements
Are willing and able to complete study requirements
Willing and able to meet all study requirements
Able and willing to give informed assent and comply with study requirements
Willing and able to meet all study requirements
Willing and able to comply with the requirements of the protocol
Patient is able to understand and comply with protocol requirements and instructions
The subject is willing and able to comply with the study protocol
Willing to follow protocol requirements
Participant is willing to be randomized and able to comply with the protocol
Willing and able to comply with trial protocol and follow-up
Willing and able to comply with trial protocol and follow-up
Willing and able to comply with trial protocol and follow-up
Willing and able to comply with trial protocol and follow-up
Subjects provide signed informed consent and confirm that they are able and willing to comply with all protocol requirements. Cohort A Only:
Willing to comply with protocol requirements
Patient is willing to comply with protocol requirements
Willing and able to follow the protocol requirements.
Not willing to comply with the procedural requirements of this protocol
Women willing to comply with protocol requirements
Patients willing to comply with protocol requirements
The patient is willing and able to comply with the study protocol
Capable and willing to comply with the entire study protocol
Patients who are able to comply with the protocol.