Extension Study to Assess Effects of Non-interrupted Versus Interrupted and Long Term Treatment of Two Dose Regimes of Secukinumab in Subjects With Hidradenitis Suppurativa

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 MULTICENTER, DOUBLE-BLIND, RANDOMIZED WITHDRAWAL EXTENSION STUDY OF SUBCUTANEOUS SECUKINUMAB TO DEMONSTRATE LONG-TERM EFFICACY, SAFETY AND TOLERABILITY IN SUBJECTS WITH MODERATE TO SEVERE HIDRADENITIS SUPPURATIVA

Intervention/treatment:
COSENTYX
Medical condition:
HIDRADENITIS SUPPURATIVA
Protocol code:
CAIN457M2301E1
Control number:
235883
Status:
Closed
Approved:
March 06, 2020
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04179175
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 100 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Study Director
Organization
Novartis Pharmaceuticals
Phone:
1 862 778 8300
Sponsor
NOVARTIS PHARMACEUTICALS CANADA INC

Locations

Ontario

Novartis Investigative Site
Barrie, Ontario, L4M 7G1
Novartis Investigative Site
London, Ontario, N6H 5L5
Novartis Investigative Site
Peterborough, Ontario, K9J 5K2
Novartis Investigative Site
Waterloo, Ontario, N2J 1C4

Results

See the results from the trial NCT04179175. 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?