drugset / Trial / NCT01482715

A Study of Oral Rucaparib in Patients With a Solid Tumor (Phase I) or With gBRCA Mutation Ovarian Cancer (Phase II)

NCT01482715

Phase 1/2 Completed 136 enrolled pharmaand GmbH Foundation Medicine · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

Part 1 (Completed Enrollment) - The purpose of the first part of the study was to evaluate the safety of different doses and dosing regimens of oral rucaparib administered daily to patients with solid tumors. Part 2A (Completed Enrollment) and Part 2B (Completed Enrollment) - The purpose of the second part of the study is to determine the safety and clinical activity of the RP2D of oral rucaparib administered daily to patients with a known deleterious BRCA mutation (germline or somatic). Part 3 (Completed Enrollment) - The purpose of the third part of the study is to further evaluate PK of higher dose strength tablets at the RP2D in patients with any advanced solid tumor, inclusive of lymphoma, with evidence of a BRCA mutation (germline or somatic).

Timeline

Start
2011-11
Primary completion
2019-03
Completion
2019-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Rucaparib Small molecule 40 mg Oral
Subject Rucaparib Small molecule 80 mg Oral
Subject Rucaparib Small molecule 160 mg Oral
Subject Rucaparib Small molecule 240 mg Oral
Subject Rucaparib Small molecule 300 mg Oral
Subject Rucaparib Small molecule 360 mg Oral
Subject Rucaparib Small molecule 480 mg Oral
Subject Rucaparib Small molecule 500 mg Oral
Subject Rucaparib Small molecule 600 mg Oral
Subject Rucaparib Small molecule 840 mg Oral