drugset / Trial / NCT05695950

A Study Evaluating the Effects of GLPG3667 Given as Oral Treatment for up to 24 Weeks in Adults With Dermatomyositis

NCT05695950 ↗

Phase 2 Completed 40 enrolled Lakefront Biotherapeutics NV
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

EvaluationDrugModalityDoseRoute
Subject GLPG3667 Small molecule — Oral

Indications