19
Participants
Start Date
June 8, 2017
Primary Completion Date
September 9, 2020
Study Completion Date
September 9, 2020
ONC201
ONC201 will be administered at a dose of 625 mg by mouth weekly until disease progression, unacceptable toxicity, or if the patient discontinues for any other reason. Radiologic tumor assessment would be performed at baseline, Cycle 3 Day 1, Cycle 5 Day 1, and at the end of every 3 cycles beyond cycle 5. All patients including those removed from the study due to unacceptable toxicity, will undergo radiologic tumor assessment at the time of discontinuation (End of treatment).
Fox Chase Cancer Center, Philadelphia
Collaborators (1)
Oncoceutics, Inc.
INDUSTRY
Fox Chase Cancer Center
OTHER