drugset / Trial / NCT00653939

A Safety and Efficacy Study of Carboplatin, Paclitaxel, Bevacizumab and CA4P in Non-Small Cell Lung Cancer

NCT00653939

Phase 2 Completed 63 enrolled Mateon Therapeutics
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, tolerability and efficacy of combretastatin A4 phosphate (CA4P), also known as fosbretabulin, in combination with bevacizumab (Avastin), carboplatin and paclitaxel in patients with chemotherapy naïve non-small cell lung cancer (NSCLC). This is a randomized parallel arm study. All participants will receive carboplatin, paclitaxel and bevacizumab, and half will additionally receive CA4P. Patients who complete the first 6 cycles of therapy and have not experienced disease progression will receive maintenance therapy with bevacizumab alone or with bevacizumab plus CA4P. The rationale for this study is the potential additive or synergistic actions of vascular disrupting agents like CA4P with anti-angiogenic agents like bevacizumab.

Timeline

Start
2008-03
Primary completion
2011-07
Completion
2011-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject fosbretabulin Small molecule 60 mg/m2
Background Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Background Carboplatin Small molecule Intravenous
Background Paclitaxel Small molecule 200 mg/m2 Intravenous

Indications