Study of Pembrolizumab (MK-3475) Plus Chemotherapy Versus Placebo Plus Chemotherapy in Participants With Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma (MK-3475-585/KEYNOTE-585)

Last updated:
2026-09-26
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, DOUBLE-BLIND, CLINICAL TRIAL OF PEMBROLIZUMAB (MK-3475) PLUS CHEMOTHERAPY (XP OR FP) VERSUS PLACEBO PLUS CHEMOTHERAPY (XP OR FP) AS NEOADJUVANT/ADJUVANT TREATMENT FOR SUBJECTS WITH GASTRIC AND GASTROESOPHAGEAL JUNCTION (GEJ) ADENOCARCINOMA (KEYNOTE-585)

Intervention/treatment:
KEYTRUDA / CISPLATIN / FLUOROURACIL / CAPECITABINE
Medical condition:
GASTROESOPHAGEAL JUNCTION CANCER
Protocol code:
585-00
Control number:
206882
Status:
Closed
Approved:
July 21, 2017
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03221426
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 0033)
Edmonton, Alberta, T6G 1Z2

New Brunswick

Moncton Hospital - Horizon Health Network ( Site 0038)
Moncton, New Brunswick, E1C 6Z8

Ontario

Sunnybrook Research Institute ( Site 0032)
Toronto, Ontario, M4N 3M5

Quebec

CHU de Quebec - Hotel-Dieu de Quebec ( Site 0042)
Quebec, Quebec, G1R 2J6
CISSS de la Monteregie-Centre ( Site 0039)
Greenfield Park, Quebec, J4V 2H1
CIUSSS de l Est de L Ile de Montreal - Hopital Maisonneuve-Rosemont ( Site 0040)
Montreal, Quebec, H1T 2M4
CIUSSS de l Estrie - CHUS - Centre Hosp. Univ. Sherbrooke ( Site 0035)
Sherbrooke, Quebec, J1H 5N4
Jewish General Hospital ( Site 0034)
Montreal, Quebec, H3T 1E2

Results

See the results from the trial NCT03221426. 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?