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SAT 3247

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Drug Profile

SAT 3247

Alternative Names: SAT-3247

Latest Information Update: 15 Oct 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

  • 10 Oct 2025 Adverse events, pharmacokinetics and efficacy data from a phase Ia/b trial in Duchenne muscular dystrophy released by Satellos Bioscience
  • 10 Oct 2025 Satellos Bioscience plans a proof-of-concept phase II trial for Duchenne muscular dystrophy (In neonates, In infants, In adolescents, In children) in USA (PO), in 2025
  • 22 Sep 2025 Satellos Biosciences files an IND application with the USFDA, MHRA, Medicines and Medical Devices Agency of Serbia, EMA, and TGA in Duchenne muscular dystrophy

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