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Clinical Trial Active — Not Recruiting Phase III NCT06840392

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

A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa — Active Not Recruiting •…

📅 05 Jun 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase III
NCT ID
NCT06840392
Start
2025-03-20
Completion
2027-06-03
ClinicaliQ Trial Snapshot
  • A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa — Active Not Recruiting • Phase III • NCT06840392.
  • Remibrutinib reduces symptoms of severe hidradenitis suppurativa better than placebo, with acceptable safety in adults and teenagers.

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What This Trial Is Studying

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). Conditions: Hidradenitis Suppurativa Interventions: Remibrutinib Dose A, Remibrutinib Dose B, Placebo 1, Placebo 2 Lead Sponsor: Novartis Pharmaceuticals Planned Enrollment: 565 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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