Single Agent ONC201 in Recurrent or Metastatic Endometrial Cancer

PHASE2TerminatedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

June 8, 2017

Primary Completion Date

September 9, 2020

Study Completion Date

September 9, 2020

Conditions
Endometrial Cancer
Interventions
DRUG

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).

Trial Locations (1)

19111

Fox Chase Cancer Center, Philadelphia

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Oncoceutics, Inc.

INDUSTRY

lead

Fox Chase Cancer Center

OTHER