Phase IIB Dose Ranging Study in Subjects With Moderate to Severe Rheumatoid Arthritis

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 PHASE IIB, RANDOMIZED, MULTI-CENTER, DOUBLE-BLIND, DOSE-RANGING STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CLAZAKIZUMAB IN SUBJECTS WITH MODERATE TO SEVERE ACTIVE RHEUMATOID ARTHRITIS WHO HAVE EXPERIENCED AN INADEQUATE RESPONSE TO TNF INHIBITORS

Intervention/treatment:
BMS-945429; ALD-518 (CLAZAKIZUMAB)/METHOTREXATE
Medical condition:
RHEUMATOID ARTHRITIS
Protocol code:
IM133-066
Control number:
170073
Status:
Closed
Approved:
December 13, 2013
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT02015520
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
Study Director
Organization
CSL Behring
Phone:
610-878-4000
Sponsor
BRISTOL-MYERS SQUIBB CANADA

Locations

Ontario

Cividino Medicine Professional Corporation
Hamilton, Ontario, L8N 2B6
Credit Valley Rheumatology
Mississauga, Ontario, L5M 2V8

Saskatchewan

Dr. Latha Naik Medical Professional Corporation
Saskatoon, Saskatchewan, S7K 3H3

Results

See the results from the trial NCT02015520. 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?