Mepolizumab as Add-on Treatment IN Participants With COPD Characterized by Frequent Exacerbations and Eosinophil Level

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 MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, PLACEBO-CONTROLLED STUDY OF MEPOLIZUMAB 100 MG SC AS ADD-ON TREATMENT IN PARTICIPANTS WITH COPD EXPERIENCING FREQUENT EXACERBATION AND CHARACTERIZED BY EOSINOPHIL LEVELS

Intervention/treatment:
MEPOLIZUMAB (SB240563)
Medical condition:
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
Protocol code:
208657
Control number:
233198
Status:
Closed
Approved:
November 28, 2019
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04133909
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

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

Contacts and locations

Contact
Name
GSK Response Center
Organization
GlaxoSmithKline
Phone:
866-435-7343
Sponsor
GLAXOSMITHKLINE INC

Locations

British Columbia

GSK Investigational Site
Vancouver, British Columbia, V5Z 4E1

Nova Scotia

GSK Investigational Site
Truro, Nova Scotia, B2N 1L2

Ontario

GSK Investigational Site
Ajax, Ontario, L1S 2J5
GSK Investigational Site
Newmarket, Ontario, L3Y 5G8
GSK Investigational Site
Sarnia, Ontario, N7T 4X3
GSK Investigational Site
Windsor, Ontario, N8X 1T3

Quebec

GSK Investigational Site
Saint-Charles-Borromée, Quebec, J6E 2B4

Results

See the results from the trial NCT04133909. 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?