drugset / Trial / NCT01928615

A Study of Subcutaneously Administered Herceptin (Trastuzumab) in Patients With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Early Breast Cancer

NCT01928615 ↗

Phase 2 Terminated 2 enrolled Hoffmann-La Roche
RandomizedCrossoverOpen-labelTreatment

Summary

This open-label, randomized crossover study evaluated the quality of life, efficacy, and safety of subcutaneous Herceptin (trastuzumab) injected either into the thigh or the upper arm of participants with early HER2-positive breast cancer.

Timeline

Start
2013-09
Primary completion
2013-10
Completion
2013-10

Outcome

Outcome not reported

Stopped: “Problems with drug supply”

Drugs

EvaluationDrugModalityDoseRoute
Subject Trastuzumab Monoclonal antibody 6 mg/kg Intravenous
Subject Trastuzumab Monoclonal antibody 600 mg Intravenous

Indications