Able and willing to give informed consent
Subject is willing and able to give prior written informed consent for investigation participation; and
Willing and able to give informed consent
Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
Willing and able to give informed consent
Patient must be willing to give written informed consent and must be able to adhere to dosing and visit schedules, and meet all study requirements.
Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
Be able and willing to give informed consent
Patients should be willing and able to give informed consent
Patients are willing and able to give informed consent (Phase II only)
Willing and able to give informed consent
Able and willing to give informed consent.
Willing and able to give informed consent
Able and willing to give informed consent.
Able and willing to give informed consent.
ORAL CAVITY SQUAMOUS CELL CARCINOMA COHORT: Willing and able to give informed consent and adhere to protocol therapy
Willing and able to give informed consent.
Willing and able to give informed consent.
Willing and able to give informed consent
Subjects must be willing to give written informed consent per institutional guidelines and must be able to adhere to dose and visit schedules
Willing and able to give informed consent and adhere to protocol therapy
Willing and able to give informed consent
Patient must be willing to give written informed consent and must be able to adhere to dosing and visit schedules, and meet all study requirements.
Willing and able to give informed consent
Willing and able to give informed consent
Willing and able to give informed consent
Subjects must be willing to give written informed consent and be able to adhere to dose and visit schedules.
Able and willing to give informed consent
Able and willing to give informed consent
Willing to give written informed consent, adhere to the visit schedules and meet study requirements
Willing and able to give informed consent and adhere to visit/protocol schedules
Subject must be able and willing to give written informed consent for a contrast enhanced ultrasound study of the prostate
Patient must be able and willing to give informed consent
Willing and able to consent and participate in the study.
Willing and able to give informed consent
Patients willing to give informed consent