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Clinical Trial Summary

This is a phase 1/phase 2a study of the combination of immune checkpoint inhibitor (nivolumab) in combination with the PARP inhibitor (rucaparib) for patients with metastatic castration resistant prostate cancer (mCRPC) and metastatic/recurrent endometrial cancer.

In the phase 1 portion, the safety of the combination dosing will be determined. If the combination dosing is determined to be safe and feasible, the study will move onto phase 2a.

In the phase 2a portion, participants will be randomized to receive either: rucaparib alone, nivolumab alone, or combination therapy (rucaparib and nivolumab).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03572478
Study type Interventional
Source University of Chicago
Contact Jaclyn Peterson
Phone 773-834-1746
Email Jdpeterson@medicine.bsd.uchicago.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date August 14, 2018
Completion date November 2022

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