drugset / Trial / NCT05437263

A Study to Investigate the Efficacy and Safety of Brepocitinib in Adults With Dermatomyositis

NCT05437263 ↗

Phase 3 Completed 241 enrolled Priovant Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a phase 3, multicenter, randomized, placebo-controlled, double-blind study of treatment with brepocitinib (TYK2/JAK1 inhibitor) in adults with dermatomyositis (DM). The primary objective of this study is to assess the efficacy of two dose levels of brepocitinib in comparison to placebo, as measured by differences in the Total Improvement Score (TIS). After 52 weeks of double-blind treatment, participants have the option to continue therapy in a 52 week open-label extension phase where all participants will receive brepocitinib.

Timeline

Start
2022-10-31
Primary completion
2025-07-17
Completion
2026-09-09

Outcome

Met primary endpoint

paper difference with brepocitinib 30 mg vs. placebo, 15.3; 95% confidence interval [CI], 6.7 to 24.0; P<0.001 PMID 41910335 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Brepocitinib Small molecule 15 mg Oral
Subject Brepocitinib Small molecule 30 mg Oral

Indications