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Research programme: congenital muscular dystrophy gene therapy - SEAL Therapeutics/Santhera Pharmaceuticals

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Drug Profile

Research programme: congenital muscular dystrophy gene therapy - SEAL Therapeutics/Santhera Pharmaceuticals

Latest Information Update: 28 Jun 2023

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At a glance

  • Originator Biozentrum, University of Basel; Rutgers
  • Developer Santhera Pharmaceuticals; SEAL Therapeutics
  • Class Gene therapies
  • Mechanism of Action Gene transference; Laminin alpha 2 replacements
  • Orphan Drug Status

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

    No
  • New Molecular Entity No

Highest Development Phases

  • No development reported Muscular dystrophies

Most Recent Events

  • 28 Jun 2023 No recent reports of development identified for preclinical development in Muscular-dystrophies in Switzerland (Parenteral)
  • 28 Feb 2022 Santhera Pharmaceuticals terminates a licensing agreement with Biozentrum,University of Basel for development of gene therapy for Muscular dystrophies
  • 28 Feb 2022 Santhera Pharmaceuticals terminates a licensing agreement with Rutgers for development of gene therapy for Muscular dystrophies

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