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Clinical Trial 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).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05695950
Study type Interventional
Source Galapagos NV
Contact Galapagos Medical Information
Phone +3215342900
Email medicalinfo@glpg.com
Status Recruiting
Phase Phase 2
Start date February 27, 2023
Completion date March 2025

See also
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