drugset / Trial / NCT01966471

A Study of Trastuzumab Emtansine (Kadcyla) Plus Pertuzumab (Perjeta) Following Anthracyclines in Comparison With Trastuzumab (Herceptin) Plus Pertuzumab and a Taxane Following Anthracyclines as Adjuvant Therapy in Participants With Operable HER2-Positive Primary Breast Cancer

NCT01966471

Phase 3 Completed 1846 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This two-arm, randomized, open-label, multicenter study will evaluate the efficacy and safety of trastuzumab emtansine in combination with pertuzumab versus trastuzumab in combination with pertuzumab and a taxane as adjuvant therapy in participants with human epidermal growth (HER) factor 2 (HER2)-positive primary invasive breast cancer. Following surgery and anthracycline-based chemotherapy, participants will receive either trastuzumab emtansine at a dose of 3.6 milligrams per kilogram (mg/kg) and pertuzumab at a dose of 420 milligrams (mg) intravenously (IV) every 3 weeks (q3w) or trastuzumab at a dose of 6 mg/kg and pertuzumab at a dose of 420 mg IV q3w in combination with a taxane.

Timeline

Start
2014-01-31
Primary completion
2019-11-27
Completion
2021-06-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Docetaxel Small molecule 75 mg/m2 Intravenous
Comparator Docetaxel Small molecule 100 mg/m2 Intravenous
Comparator Paclitaxel Small molecule 80 mg/m2 Intravenous
Comparator Pertuzumab Monoclonal antibody 420 mg Intravenous
Comparator Trastuzumab Monoclonal antibody 6 mg/kg Intravenous
Subject Trastuzumab emtansine Other / unclassified 3.6 mg/kg Intravenous
Background Cyclophosphamide Other / unclassified
Background Doxorubicin Other / unclassified
Background Epirubicin Small molecule
Background fluorouracil Small molecule

Indications