Phase 1/2 MAD clinical study of ENTR-601-50 in ambulatory patients living with DMD
Latest Information Update: 22 Jan 2026
At a glance
- Drugs ENTR 601 50 (Primary)
- Indications Duchenne muscular dystrophy
- Focus Adverse reactions
- Acronyms ELEVATE-50-201
Most Recent Events
- 22 Jan 2026 New trial record
- 08 Jan 2026 According to Entrada Therapeutics media release, company expects to submit regulatory applications in the EU for ENTR-601-50 in the second half of 2026 and initiate the study by the end of 2026.
- 08 Jan 2026 According to Entrada Therapeutics media release, company has received regulatory authorization from the U.K.s Medicines and Healthcare Products Regulatory Agency (MHRA) and Research Ethics Committee to initiate a Phase 1/2 MAD clinical study of ENTR-601-50 in ambulatory patients living with DMD who are amenable to exon 50 skipping.