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Study of SRP-1003 in Participants With Type 1 Myotonic Dystrophy

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NCT06138743 · readout in 134 d

Sponsored by Sarepta Therapeutics, Inc. (industry) · SRPT — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
78estimated
Sites
35
Countries
Australia, Belgium, Canada +8

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-03-04actualWhen the study began enrolling
Primary completion2026-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-31estimatedThe whole study's end, after follow-up
First posted2023-11-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Myotonic Dystrophy 1

Interventions

  • Drug: SRP-1003 IV Infusion — also filed as ARO-DM1 IV Infusion
  • Drug: Placebo IV Infusion
  • Drug: SRP-1003 SC Injection — also filed as ARO-DM1 SC Injection
  • Drug: Placebo SC Injection

Primary outcome

what the primary-completion date above is the date OF
Number of Participants with Treatment-emergent Adverse Events Over Time Through End of Study (EOS)
measured Single-dose phase (Part 1): Up to Day 90 (EOS); multiple-dose phase (Part 2): Up to Day 180 (EOS)

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