drugset / Trial / NCT00850577

Ph II of a Novel Anti-angiogenic Agent in Combination With Chemotherapy for the Treatment of Non-Small Cell Lung Cancer

NCT00850577

Phase 2 Terminated 255 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the efficacy of CT-322 comparative to bevacizumab, both in combination with carboplatin and paclitaxel in the treatment of chemonaive subjects with recurrent or advanced non-squamous NSCLC

Timeline

Start
2009-06
Primary completion
2013-08
Completion
2013-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Comparator PEGDINETANIB Protein / enzyme biologic 2 mg/kg Intravenous
Comparator Carboplatin Small molecule 6 unknown Intravenous
Comparator Paclitaxel Small molecule 200 mg/m2 Intravenous