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Title:
A Phase 2, Open-Label Study of Rucaparib in Patients with Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer (CO-338-017)
Protocol Number:
J1395
Phase:
Phase II
Physician:
Deborah Armstrong
Purpose:
- To determine the efficacy of Rucaparib - To evaluate progression free survival
Eligibility:
- Recurrent platinum sensitive ovarian, fallopian tube or primary peritoneal cancer - Platinum sensitive disease is defined as progression greater than 6 months after last dose of platinum agent - must have a biopsy prior to starting on study - measurable disease - Good lab results and performace status
Treatment:
Treatment is with an oral drug (Rucaparib) that is taken twice a day. It is given on an outpatient basis. You will be given a 28 day supply. There are additional lab and scan requirements.
Population:
Adult
Last Update
08/28/2014 04:23 AM
 

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