Omigapil

Drug Profile

Omigapil

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

Latest Information Update: 04 Nov 2017

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At a glance

  • Originator Novartis
  • Developer Novartis; Santhera Pharmaceuticals
  • Class 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

  • Phase I Muscular dystrophies
  • Discontinued Amyotrophic lateral sclerosis; Motor neuron disease; Parkinson's disease

Most Recent Events

  • 04 Nov 2017 No recent reports of development identified for preclinical development in Muscular-dystrophies in Switzerland (PO)
  • 15 Dec 2016 Biomarkers information updated
  • 01 May 2016 Omigapil receives Fast Track designation for Muscular dystrophies [PO] (In adolescents, In children) in USA
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