drugset / Trial / NCT00463788

Cetuximab and Cisplatin in the Treatment of "Triple Negative" (Estrogen Receptor [ER] Negative, Progesterone Receptor [PgR] Negative, and Human Epidermal Growth Factor Receptor 2 [HER2] Negative) Metastatic Breast Cancer

NCT00463788 ↗

Phase 2 Completed 181 enrolled Merck KGaA, Darmstadt, Germany
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine whether overall response to cetuximab combined with cisplatin is better than overall response to cisplatin alone together with showing that the overall response for cetuximab and cisplatin was above a pre-specified threshold of 0.2 in the treatment of "triple negative" metastatic breast cancer. The secondary objective of this study is to compare the differences between the two treatment groups using the following criteria : Progression-Free Survival (PFS) Time, Overall Survival (OS), Time to Response (TTR) and Safety.

Timeline

Start
2007-06
Primary completion
2009-07
Completion
2011-02

Outcome

Missed primary endpoint

registry analysis (superiority or other test); Cisplatin and Cetuximab vs Cisplatin; p = 0.1109; Odds Ratio (OR) 2.126 (95% CI 0.809 to 5.591); NCT00463788 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 250 mg/m2 Intravenous
Comparator Cisplatin Other / unclassified 75 mg/m2 Intravenous

Indications