drugset / Trial / NCT02163694

A Phase 3 Randomized, Placebo-controlled Trial of Carboplatin and Paclitaxel With or Without Veliparib (ABT-888) in HER2-negative Metastatic or Locally Advanced Unresectable BRCA-associated Breast Cancer

NCT02163694

Phase 3 Completed 513 enrolled AbbVie
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the study is to assess the progression-free survival (PFS) of veliparib in combination with carboplatin and paclitaxel (C/P) compared to placebo plus C/P in participants with a Breast Cancer Gene 1 or 2 (BRCA1; BRCA2) mutation in Human Epidermal Growth Factor Receptor 2 (HER2)-negative metastatic or locally advanced unresectable breast cancer. The secondary objectives of the study are to assess overall survival (OS), clinical benefit rate (CBR) through the end of Week 24, objective response rate (ORR) and PFS on subsequent therapy (PFS2) in participants treated with veliparib in combination with C/P versus placebo in combination with C/P.

Timeline

Start
2014-04-08
Primary completion
2019-04-05
Completion
2024-01-25

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Veliparib Small molecule 120 mg Oral
Background Carboplatin Small molecule 6 unknown Intravenous
Background Paclitaxel Small molecule 80 mg/m2 Intravenous

Indications