drugset / Trial / NCT01401166

Participant Preference of Subcutaneous (SC) Versus Intravenous (IV) Herceptin (Trastuzumab) in Human Epidermal Growth Factor Receptor (HER) 2-Positive Early Breast Cancer

NCT01401166 ↗

Phase 2 Completed 488 enrolled Hoffmann-La Roche
RandomizedCrossoverOpen-labelHealth-services research

Summary

This randomized, open-label, crossover study will evaluate participants' preference and healthcare professional (HCP) satisfaction with SC versus IV Herceptin administration in HER2-positive early breast cancer. Participants will be randomized to receive either SC Herceptin or IV Herceptin every 3 weeks for Cycles 1 to 4, followed by crossover to the other treatment administration for Cycles 5 to 8. For up to 10 additional cycles (for a total of 18 cycles), participants will receive IV or SC Herceptin every 3 weeks.

Timeline

Start
2011-10
Primary completion
2013-05
Completion
2015-12

Outcome

Met primary endpoint

paper s.c. was preferred by 415/467 [88.9%; 95% confidence interval (CI) 85.7-91.6; P < 0.0001; two-sided test against null hypothesis of 65% s.c. preference] PMID 25070545 ↗

Publications

Drugs

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

Indications