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Clinical Trial ● Currently Recruiting Phase III NCT07486934

Efficacy, Safety, and Tolerability of Zeleciment Basivarsen (DYNE-101) in Participants With Myotonic Dystrophy Type 1

Efficacy, Safety, and Tolerability of Zeleciment Basivarsen (DYNE-101) in Participants With Myotonic Dystrophy Type 1 — Recruiting • Phase III • NCT07486934.

📅 14 Jul 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07486934
Start
2026-05-14
Completion
2028-07
ClinicaliQ Trial Snapshot
  • Efficacy, Safety, and Tolerability of Zeleciment Basivarsen (DYNE-101) in Participants With Myotonic Dystrophy Type 1 — Recruiting • Phase III • NCT07486934.
  • A drug called zeleciment basivarsen was tested to see if it safely and effectively treats myotonic dystrophy type 1.

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What This Trial Is Studying

The purpose of the study is to assess the efficacy, safety, and tolerability of zeleciment basivarsen (DYNE-101) for the treatment of myotonic dystrophy 1 (DM1). Conditions: Myotonic Dystrophy Type 1 (DM1), DM1, Myotonic Dystrophy, Steinert Disease, Steinert Interventions: zeleciment basivarsen (DYNE-101), Placebo Lead Sponsor: Dyne Therapeutics Planned Enrollment: 150 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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