U.S., Jan. 30 -- ClinicalTrials.gov registry received information related to the study (NCT06799000) titled 'A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult Patients With Moderate to Severe Hidradenitis Suppurativa' on Jan. 23.
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).
Study Start Date: March 12
Study Type: INTERVENTIONAL
Condition:
Hidradenitis Suppurativa
Intervention:
DRUG: Remibrutinib Dose A
Remibrutinib Dose A (oral)
DRUG: Remibrutinib Dose B
Remibrutinib Dose B (oral)
DRUG: Placebo 1
Placebo matching t...