73
Participants
Start Date
November 10, 2016
Primary Completion Date
February 28, 2025
Study Completion Date
January 31, 2027
Bevacizumab
"* Bevacizumab will be given intravenously at a pre-determined dosage~* One dose reduction will be allowed for Bevacizumab"
Nivolumab
"* Nivolumab injection is to be administered as an IV infusion at a pre-determined dosage.~* No dose reductions or escalations will be allowed for Nivolumab"
Rucaparib
"* Rucaparib will be taken orally twice daily on days 1-14 at a pre-determined dosage.~* Up to three dose reductions will be allowed for Rucaparib (depending on cohort)."
Massachusetts General Hospital, Boston
Dana Farber Cancer Institute, Boston
Beth Israel Deaconess Medical Center, Boston
Collaborators (2)
Bristol-Myers Squibb
INDUSTRY
Clovis Oncology, Inc.
INDUSTRY
Dana-Farber Cancer Institute
OTHER