Patients must be able to understand and agree to sign an institutional review board (IRB)-approved informed consent form
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
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigators 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 investigators Institutional Review Board (IRB)/Ethics Committee
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 investigators Institutional Review Board (IRB)/ethics committee
Patient or durable power of attorney (DPA) for healthcare must be able to 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
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's IRB/Ethics Committee
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigators Institutional Review Board (IRB)/Ethics Committee
Relapsed/refractory MCL: Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Patients must be able to understand and agree to sign an Institutional Review Board (IRB)-approved informed consent form
Understanding and voluntarily signing 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
FOR TISSUE COLLECTION TO ESTABLISH PDX (PART ): Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form.
DONOR: The donor or legal guardian greater than  years of age, capable of signing an Institutional Review Board (IRB)-approved consent form
Understanding and voluntary signing an institutional review board (IRB)-approved informed consent form
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 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
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
Patients must agree to randomization as documented by signing the Institutional Review Board (IRB) approved consent form
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
Understanding and voluntary signing an Institutional Review Board (IRB)-approved informed consent form
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
Competent to sign and date an Institutional Review Board approved informed consent form
Patient or durable power of attorney (DPA) for healthcare must be able to understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Able to understand and sign an Institutional Review Board (IRB)-approved informed consent form
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
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