Who Can Participate?
Adults (18+) with moderate to severe hidradenitis suppurativa (HS) may participate.
Inclusion Criteria
What Are The Benefits?
How Long Will The Study Last?
Edmonton - Alberta DermaSurgery Centre
Las Vegas - Vivida Dermatology
London - DermEffects
No Doctors Found
Similar Trials
No Similar Trials FoundThe following information is from ClinicalTrials.gov
Last Update Posted: June 10, 2025
NCT06840392
Novartis Pharmaceuticals
Brief Summary:
The purpose of this study is to establish the efficacy, safety, and tolerability of remibrutinib (LOU064) Dose A and Dose B compared to placebo in participants with moderate to severe hidradenitis suppurativa (HS).
Condition or Disease:
Hidradenitis Suppurativa
Intervention/Treatment:
Drug: Remibrutinib Dose A Drug: Remibrutinib Dose B Drug: Remibrutinib Dose B,Drug: Placebo 1,Drug: Placebo 2Phase:
PHASE3
Ages Eligible for Study:
18 Years and 100 Years (ADULT,OLDER_ADULT)
Sexes Eligible for Study:
ALL
Terms and Conditions – ClinicalTrials.gov
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Last Revised July 2024
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