PGN EDODM1
Alternative Names: EDODM1; PGN-EDODM1Latest Information Update: 16 Aug 2024
At a glance
- Originator Pepgen Corporation
- Class Antisense oligonucleotides; Drug conjugates; Morpholines; Peptide drug conjugates
- Mechanism of Action RNA interference; RNA splicing modulators
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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
- Phase I Myotonic dystrophy
Most Recent Events
- 08 Aug 2024 Health Canada and the United Kingdom Medicines and Healthcare products Regulatory Agency approves Clinical trial application (CTA) for the FREEDOM2 trial of PGN EDODM1 in Myotonic dystrophy type 1 (DM1)
- 08 Aug 2024 PepGen plans a phase II FREEDOM2-DM1 trial in Myotonic dystrophy type 1 in Canada, the UK, and in the US, subject to regulatory clearance, in the second half of 2024
- 06 Mar 2024 Phase-I clinical trials in Myotonic dystrophy in USA, and United Kingdom (IV)