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Study details
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A Phase 3 Trial of Remibrutinib for Hidradenitis Suppurativa

Novartis Pharmaceuticals
NCT IDNCT06799000ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

555

Study length

about 3.7 years

Ages

12–100

Locations

36 sites in AR, AZ, CA +18

What this study is about

This trial is testing whether remibrutinib, a medication, is effective and safe in treating moderate to severe hidradenitis suppurativa. Participants will receive either placebo or different doses of remibrutinib over 1358 days.

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