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Omigapil - Santhera Pharmaceuticals

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Drug Profile

Omigapil - Santhera Pharmaceuticals

Alternative Names: CGP 3466; CGP 3466 maleate; CGP 3466B; SNT 317; TCH 346

Latest Information Update: 28 Feb 2021

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At a glance

  • Originator Novartis
  • Developer Novartis; Santhera Pharmaceuticals
  • Class Antiparkinsonians; Neuroprotectants; Oxepins; Small molecules
  • Mechanism of Action Apoptosis inhibitors; Glyceraldehyde 3 phosphate dehydrogenase inhibitors
  • Orphan Drug Status

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

    Yes - Muscular dystrophies
  • New Molecular Entity Yes

Highest Development Phases

  • No development reported Muscular dystrophies
  • Discontinued Amyotrophic lateral sclerosis; Motor neuron disease; Parkinson's disease

Most Recent Events

  • 28 Feb 2021 No recent reports of development identified for phase-I development in Muscular-dystrophies(In adolescents, In children) in USA (PO, Liquid)
  • 05 Apr 2018 Interim pharmacokinetic and adverse events data from the phase I CALLISTO trial in Muscular-dystrophies released by Santhera Pharmaceuticals
  • 05 Apr 2018 Santhera Pharmaceuticals completes the phase I CALLISTO trial in Muscular-dystrophies in USA (NCT01805024)
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