drugset / Trial / NCT05695950
A Study Evaluating the Effects of GLPG3667 Given as Oral Treatment for up to 24 Weeks in Adults With Dermatomyositis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the efficacy, safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of orally administered GLPG3667 once daily for 24 weeks in adult participants with dermatomyositis (DM), followed by an open-label extension (OLE) period until Week 48.
Timeline
- Start
- 2023-02-27
- Primary completion
- 2025-10-13
- Completion
- 2026-04-20
Outcome
Met primary endpoint
release “The GALARISSO DM study met its primary endpoint, showing that GLPG3667” lakefrontbio.com ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GLPG3667 | Small molecule | — | Oral |