A Study Evaluating Trastuzumab Emtansine Plus Pertuzumab Compared With Chemotherapy Plus Trastuzumab and Pertuzumab for Participants With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Breast Cancer

Last updated:
2026-07-11
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol title:

A RANDOMIZED, MULTICENTER, OPEN-LABEL, TWO-ARM, PHASE III NEOADJUVANT STUDY EVALUATING TRASTUZUMAB EMTANSINE PLUS PERTUZUMAB COMPARED WITH CHEMOTHERAPY PLUS TRASTUZUMAB AND PERTUZUMAB FOR PATIENTS WITH HER-2 POSITIVE BREAST CANCER

Intervention/treatment:
KADCYLA/ PERTUZUMAB/ TRASTUZUMAB/ DOCETAXEL/ CARBOPLATIN/ SODIUM PERTECHNETATE TC-99M
Medical condition:
BREAST CANCER HER2-POSITIVE
Protocol code:
BO28408/TRIO021
Control number:
173473
Status:
Closed
Approved:
April 30, 2014
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02131064
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Medical Communications
Organization
Hoffmann-La Roche
Phone:
800 821-8590
Sponsor
HOFFMANN-LA ROCHE LIMITED

Locations

CHU de Québec - Hôpital du Saint-Sacrement / ONCOLOGY
Québec, G1S 4L8

Alberta

Cross Cancer Institute ; Dept of Medical Oncology
Edmonton, Alberta, T6G 1Z2

Ontario

St. Michael'S Hospital
Toronto, Ontario, M5B 1W8
Sunnybrook Health Sciences Centre
Toronto, Ontario, M4N 3M5

Quebec

Chum Hospital Notre Dame
Montreal, Quebec, H2L 4M1
McGill University; Sir Mortimer B Davis Jewish General Hospital; Oncology
Montreal, Quebec, H3T 1E2

Results

See the results from the trial NCT02131064. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?