A Study to Evaluate Rucaparib in Participants With Solid Tumors and With Deleterious Mutations in HRR Genes
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- pharmaand GmbH
- Study ID
- NCT04171700
- Phase
- PHASE2
- Status
- Terminated
Conditions
- Solid Tumor
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Rucaparib — DRUGOral rucaparib will be administered twice daily. The starting dose will be 600 mg daily (BID).
Study Details
A Phase 2, open-label, single-arm trial to evaluate the response of rucaparib in participants with various solid tumors and with deleterious mutations in Homologous Recombination Repair (HRR) genes.
Key Dates
- Start date
- Jan 16, 2020
- Status verified
- Sep 2023
- Primary completion
- Jun 8, 2022
- Completion
- Jul 15, 2022
Study Design
- Enrollment
- 83 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: RucaparibEligible participants will be enrolled in either Cohort A or Cohort B. Cohort A: Up to 200 participants with deleterious mutations in BRCA1, BRCA2, PALB2, RAD51C or RAD51D. Cohort B (Exploratory): Up to 20 participants with deleterious mutations in BARD1, BRIP1, FANCA, NBN, RAD51 or RAD51B.
Primary Outcome Measure
Best Overall Response Rate by Investigator [ Time Frame: From first dose of study drug until disease progression (up to approximately 2 years) ]
Locations (19)
Find similar trials in Los Angeles, CA
By research site
UCLA Medicine Hematology and Oncology· Los Angeles, CAUCSF Helen Diller Family Comprehensive Cancer Center· San Francisco, CAFlorida Cancer Specialists· Fort Myers, FLFlorida Cancer Specialists· St. Petersburg, FLH. Lee Moffitt Cancer Center & Research Institute· Tampa, FLRobert H. Lurie Comprehensive Cancer Center of Northwestern University· Chicago, IL
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