This Was a Study of Efficacy and Safety of Two Secukinumab Dose Regimens in Subjects With Moderate to Severe Hidradenitis Suppurativa (HS).

Last updated:
2026-09-12
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, MULTICENTER STUDY ASSESSING SHORT (16 WEEKS) AND LONG-TERM EFFICACY (UP TO 1 YEAR), SAFETY, AND TOLERABILITY OF 2 SUBCUTANEOUS SECUKINUMAB DOSE REGIMENS IN ADULT PATIENTS WITH MODERATE TO SEVERE HIDRADENITIS SUPPURATIVA (SUNSHINE)

Intervention/treatment:
COSENTYX (SECUKINUMAB (RECOMBINANT MONOCLONAL ANTI-HUMAN IL-17A ANTIBODY OF THE IGG1/K-CLASS)
Medical condition:
HIDRADENITIS SUPPURATIVA
Protocol code:
CAIN457M2301
Control number:
222153
Status:
Closed
Approved:
December 24, 2018
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03713619
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
Novarts Pharmaceuticals
Phone:
+1 (862) 778-8300
Sponsor
NOVARTIS PHARMACEUTICALS CANADA INC

Locations

Ontario

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 NCT03713619. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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