DT 200
Alternative Names: DT-200; G 100192; GLPG-0492; SARMs - Galapagos NVLatest Information Update: 16 Oct 2025
At a glance
- Originator ProSkelia
- Developer Akashi Therapeutics; Galapagos NV
- Class Small molecules
- Mechanism of Action Selective androgen receptor modulators
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Orphan Drug Status
No
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Phase I Duchenne muscular dystrophy
- Discontinued Cachexia
Most Recent Events
- 16 Oct 2025 Phase-I clinical trials in Duchenne muscular dystrophy (In volunteers) in United Kingdom (PO), prior to October 2025(EudraCT2016-004100-62)(Akashi Therapeutics pipeline, October 2025)
- 22 Feb 2023 Preclinical development in Duchenne muscular dystrophy is ongoing in USA (PO) (Akashi therapeutics pipeline, February 2023)
- 28 Oct 2018 No recent reports of development identified for preclinical development in Duchenne muscular dystrophy in USA (PO)