drugset / Trial / NCT02472964

Study of Efficacy and Safety of Myl1401O + Taxane vs Herceptin©+ Taxane for 1st Line, Met. Br. Ca.

NCT02472964

Phase 3 Completed 500 enrolled Mylan Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A multicenter, double-blind, randomized, parallel-group, Phase III study of the efficacy and safety of Hercules( Myl 1401O, Mylan Trastuzumab) plus taxane versus Herceptin® plus taxane as first line therapy in patients with HER2-positive metastatic breast cancer.

Timeline

Start
2012-07
Primary completion
2016-03
Completion
2018-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Hercules Unknown 6 mg/kg Intravenous
Comparator Trastuzumab Monoclonal antibody 6 mg/kg Intravenous
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Paclitaxel Small molecule 80 mg/m2 Intravenous

Indications