Study of Pembrolizumab Given Prior to Surgery and in Combination With Radiotherapy Given Post-surgery for Advanced Head and Neck Squamous Cell Carcinoma (MK-3475-689)

Last updated:
2026-08-01
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 PHASE III, RANDOMIZED, OPEN-LABEL STUDY TO EVALUATE PEMBROLIZUMAB AS NEOADJUVANT THERAPY AND IN COMBINATION WITH STANDARD OF CARE AS ADJUVANT THERAPY FOR STAGE III-IVA RESECTABLE LOCOREGIONALLY ADVANCED HEAD AND NECK SQUAMOUS CELL CARCINOMA (LA HNSCC)

Intervention/treatment:
KEYTRUDA / CISPLATIN / FLUDEOXYGLUCOSE 18F
Medical condition:
SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK
Protocol code:
689
Control number:
210521
Status:
Active, not recruiting
Approved:
November 22, 2017
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03765918
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
Senior Vice President, Global Clinical Development
Organization
Merck Sharp & Dohme LLC
Phone:
1-800-672-6372
Sponsor
MERCK CANADA INC

Locations

Alberta

Cross Cancer Institute ( Site 0201)
Edmonton, Alberta, T6G 1Z2

Ontario

Princess Margaret Cancer Centre ( Site 0202)
Toronto, Ontario, M5G 2M9
Sunnybrook Research Institute ( Site 0211)
Toronto, Ontario, M4N 3M5

Quebec

Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Univer ( Site 0209)
Sherbrooke, Quebec, J1H 5N4
McGill University Health Centre ( Site 0210)
Montreal, Quebec, H4A 3J1

Results

See the results from the trial NCT03765918. 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?