DYNE 301
Alternative Names: DYNE-301; Facioscapulohumeral muscular dystrophy therapy - Dyne TherapeuticsLatest Information Update: 28 Jul 2025
At a glance
- Originator Dyne Therapeutics
- Class Antisense oligonucleotides; Drug conjugates; Fab fragments; Immunoconjugates
- Mechanism of Action DUX4L1 protein expression inhibitors; RNA interference
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- No development reported Facioscapulohumeral muscular dystrophy
Most Recent Events
- 28 Jul 2025 No recent reports of development identified for preclinical development in Facioscapulohumeral-muscular-dystrophy in USA (Parenteral)
- 13 Oct 2021 Dyne Therapeutics announces intention to submit IND for DYNE 301 in Facioscapulohumeral muscular dystrophy (FSHD) in the second half of 2022
- 25 Jun 2021 Preclinical trials in Facioscapulohumeral muscular dystrophy in USA (Parenteral)