A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa

Running, not enrolling · Phase 3 · Has a placebo group

Conditions studied: Hidradenitis Suppurativa

In brief

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).

Key facts

Study ID
NCT06840392
Run by
Novartis Pharmaceuticals
People needed
565
Starts
2025-03-20
Expected to finish
2027-10-21
Last updated by the study team
2026-06-05

Who can join

Age: 12 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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