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Study details
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Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult Patients With Moderate to Severe Hidradenitis Suppurativa

Novartis Pharmaceuticals
NCT IDNCT06840392ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

555

Study length

about 3.6 years

Ages

12–100

Locations

36 sites in AL, AZ, CA +15

What this study is about

This trial is testing a treatment called remibrutinib compared to placebo in adults with moderate to severe hidradenitis suppurativa. The goal is to see if this treatment is effective, safe, and well-tolerated.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Placebo 1
  • 2.Take Placebo 2
  • 3.Take Remibrutinib Dose A
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Drug routes

oral (Oral Tablet)

Endpoints

Secondary: Incidence of treatment emergent adverse events and serious adverse events during the study, Percentage change from baseline in International Hidradenitis Suppurativa Severity Score System (IHS4) at Week 16, Proportion of participants with clinical response in HS related skin pain (NRS 30), at worst at Week 16