Able to provide valid written informed consent
Able and willing to give valid written informed consent.
Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent; in patients who are not able to consent to the trial due to medical circumstances, the next of kin or power of attorney may consent for the study
Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent
Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent
Able to provide valid written informed consent.
Able and willing to give valid written informed consent
Able and willing to give valid written consent for available archival tumor samples or fresh tumor biopsies/resections
Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent
Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent
Able and willing to give valid written informed consent.
Able and willing to give valid written informed consent
Signed written informed consent; patient must be capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent
Able and willing to give valid written informed consent
Able and willing to give valid written informed consent.
Able and willing to give valid written informed consent.
Able and willing to give valid written consent for archival tumor samples
Able and willing to give valid written consent for biopsy samples (subjects in the expansion phase only).
Able and willing to give valid written informed consent.
Participant or legal guardian, in the opinion of the investigator, is capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent; a signed informed consent must be obtained prior to any study specific procedures
Valid email address
Has a valid driver’s license
Patients who cannot provide a valid consent
RANDOMIZED CONTROLLED TRIAL: Must also have a valid email address
Signed written informed consent (patient must be capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent)
Patients who because of age, general medical or psychiatric condition, or physiologic status cannot give valid informed consent
Patients who because of age, general medical or psychiatric condition, or physiologic status cannot give valid informed consent
Patients who because of general medical or psychiatric condition or physiologic status cannot give valid informed consent
Patient is able and willing to give valid written informed consent
Patients who because of age, general medical or psychiatric condition, or physiologic status unrelated to the presence of prostate cancer are unlikely to be candidates for repeat MRIs, or cannot give valid informed consent
Valid informed consent by subject