A Study of Rucaparib in Patients With Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer (ARIEL2)
Part of paid clinical trials in Anchorage, Alaska.
- Sponsor
- pharmaand GmbH
- Study ID
- NCT01891344
- Phase
- PHASE2
- Status
- Completed
Conditions
- Epithelial Ovarian Cancer
- Fallopian Tube Cancer
- Ovarian Cancer
- Peritoneal Cancer
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Oral rucaparib — DRUG600 mg BID
Study Details
The purpose of this study is to determine which patients with ovarian, fallopian tube, and primary peritoneal cancer will best respond to treatment with rucaparib.
Key Dates
- Start date
- Oct 30, 2013
- Status verified
- Jun 2023
- Primary completion
- Nov 5, 2019
- Completion
- Sep 28, 2021
Study Design
- Enrollment
- 491 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Ovarian cancerrucaparib
Primary Outcome Measure
Progression-free Survival (PFS) According to RECIST v1.1 in Molecularly-defined HRD (Homologous Recombination Deficiency) Subgroups (Part 1 of Study) [ Time Frame: Assessments every 8 weeks from C1D1 until disease progression, death or withdrawal of consent. After 18 months on study, assessments every 16 weeks. Total follow-up was up to approximately 3 years. ]
Locations (36)
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