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A phase 1 randomized, placebo-controlled, double-blind, multiple ascending dose (MAD) clinical trial studying DYNE-302 for treatment of facioscapulohumeral muscular dystrophy (FSHD)

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Trial Profile

A phase 1 randomized, placebo-controlled, double-blind, multiple ascending dose (MAD) clinical trial studying DYNE-302 for treatment of facioscapulohumeral muscular dystrophy (FSHD)

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 05 Aug 2026

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At a glance

  • Drugs DYNE 302 (Primary)
  • Indications Facioscapulohumeral muscular dystrophy
  • Focus Adverse reactions

Most Recent Events

  • 28 Jul 2026 According to Dyne Therapeutics media release, the company received clearance from the U.S. Food and Drug Administration (FDA) for its IND application to initiate a Phase 1 clinical trial for DYNE-302 in facioscapulohumeral muscular dystrophy (FSHD).
  • 17 Jun 2024 New trial record
  • 13 Jun 2024 According to Dyne Therapeutics media release, the company is looking forward to progressing through IND/CTA-enabling studies.

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