drugset / Trial / NCT01774786

A Study of Pertuzumab in Combination With Trastuzumab and Chemotherapy in Participants With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Metastatic Gastroesophageal Junction or Gastric Cancer

NCT01774786

Phase 3 Completed 780 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This double-blind, placebo-controlled, randomized, multicenter, international, parallel arm study will evaluate the efficacy and safety of pertuzumab in combination with trastuzumab, fluoropyrimidine and cisplatin as first-line treatment in participants with HER2-positive metastatic gastroesophageal junction (GEJ) or gastric cancer (GC). Participants will be randomized to receive pertuzumab 840 milligrams (mg) or placebo intravenously every 3 weeks (q3w) in combination with trastuzumab (initial dose of 8 milligrams per kilogram \[mg/kg\] intravenously \[IV\] followed by 6 mg/kg IV q3w) and cisplatin and fluoropyrimidine (capecitabine or 5-fluorouracil) for the first 6 treatment cycles. Participants will continue to receive pertuzumab or placebo and trastuzumab until disease progression occurrence of unacceptable toxicity or withdrawal from the study for another reason.

Timeline

Start
2013-06-10
Primary completion
2016-12-09
Completion
2019-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pertuzumab Monoclonal antibody 840 mg Intravenous
Background Capecitabine Small molecule 1000 mg/m2 Oral
Background Cisplatin Other / unclassified 80 mg/m2 Intravenous
Background Trastuzumab Monoclonal antibody 6 mg/kg Intravenous
Background fluorouracil Small molecule 800 mg/m2 Intravenous

Indications