drugset / Trial / NCT00938652

A Phase 3, Multi-Center Study of Gemcitabine/Carboplatin, With or Without BSI-201, in Patients With ER-, PR-, and Her2-Negative Metastatic Breast Cancer

NCT00938652

Phase 3 Completed 519 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

The goal of this study was to determine the effect on overall survival and progression free survival by adding iniparib (BSI-201/SAR240550) to the combination of gemcitabine/carboplatin in adult patients with triple negative breast cancer (estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and human epidermal growth factor receptor 2 (HER2)-negative). Based on data generated by BiPar/Sanofi, it is concluded that iniparib does not possess characteristics typical of the poly (ADP-ribose) polymerase (PARP) inhibitor class. The exact mechanism has not yet been fully elucidated, however based on experiments on tumor cells performed in the laboratory, iniparib is a novel investigational anti-cancer agent that induces gamma-H2AX (a marker of DNA damage) in tumor cell lines, induces cell cycle arrest in the G2/M phase in tumor cell lines, and potentiates the cell cycle effects of DNA damaging modalities in tumor cell lines. Investigations into potential targets of iniparib and its metabolites are ongoing.

Timeline

Start
2009-07
Primary completion
2011-01
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Iniparib Small molecule 5.6 mg/kg Intravenous
Background Carboplatin Small molecule 2 unknown Intravenous
Background Gemcitabine Small molecule 1000 mg/m2 Intravenous

Indications