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SAT 3247

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Drug Profile

SAT 3247

Alternative Names: SAT-3247

Latest Information Update: 12 Dec 2025

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At a glance

  • Originator Satellos Bioscience
  • Class Small molecules
  • Mechanism of Action Adaptor-associated kinase 1 inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Duchenne muscular dystrophy
  • New Molecular Entity Yes

Highest Development Phases

  • Phase II Duchenne muscular dystrophy
  • Preclinical Facioscapulohumeral muscular dystrophy; Muscle injury

Most Recent Events

  • 09 Dec 2025 Human Research Ethics Committee (HREC) accepted the Therapeutic Goods Administration’s (TGA’s) Clinical Trial Notification (CTN) scheme for regulatory authorization of SAT 3247 in Duchenne muscular dystrophy
  • 09 Dec 2025 The Medicine and Healthcare products Regulatory Agency (MHRA) granted authorization to Clinical Trial Application (CTA) for SAT 3247 in Duchenne muscular dystrophy
  • 09 Dec 2025 The Medicines and Medical Devices Agency of Serbia (ALIMS) approved CTA for SAT 3247 in Duchenne muscular dystrophy

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