drugset / Trial / NCT01301729

A Study of Herceptin (Trastuzumab) in Combination With a Taxane in Participants With HER2-Positive Breast Cancer Who Relapsed After (Neo)Adjuvant Herceptin Treatment

NCT01301729

Phase 4 Completed 32 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This single arm, open-label study will evaluate the efficacy and safety of Herceptin (trastuzumab) in combination with a taxane as first line therapy in participants with HER2-positive breast cancer who relapsed after neoadjuvant or adjuvant Herceptin treatment. Participants will receive Herceptin (loading dose of 4 mg/kg intravenously \[iv\], 2 mg/kg iv weekly thereafter) with 6 3-week cycles of either docetaxel (100 mg/m2 iv every 3 weeks) or paclitaxel (90 mg/m2 every week). Herceptin treatment will be continued until disease progression or unacceptable toxicity occurs.

Timeline

Start
2011-03
Primary completion
2014-07
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 100 mg/m2 Intravenous
Subject Paclitaxel Small molecule 90 mg/kg Intravenous
Subject Trastuzumab Monoclonal antibody 2 mg/kg Intravenous

Indications