drugset / Trial / NCT00876486

Evaluate the Efficacy and Safety of Genexol®-PM Compared to Genexol® in Recurrent or Metastatic Breast Cancer

NCT00876486 ↗

Phase 3 Completed 213 enrolled Samyang Biopharmaceuticals Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

Phase III trial to evaluate the efficacy and safety of Genexol®-PM compared to Genexol® in subjects with recurrent or metastatic breast cancer.

Timeline

Start
2008-12
Primary completion
2013-02
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Paclitaxel Small molecule 175 mg/m2 Intravenous
Comparator Paclitaxel Small molecule 260 mg/m2 Intravenous

Indications