drugset / Trial / NCT02505048

A Study to Assess the Efficacy of Rucaparib in Metastatic Breast Cancer Patients With a BRCAness Genomic Signature

NCT02505048

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy of a PARP inhibitor, rucaparib, in progressing breast cancer patients and who are carrying a BCRAness profile defined by genomic signature or BRCA 1 or 2 somatic mutation, without known BRCA 1 or 2 germline mutation.

Timeline

Start
2016-03
Primary completion
2019-02
Completion
2019-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Rucaparib Small molecule 600 mg Oral

Indications