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Research programme: antisense oligonucleotide therapies - NeuBase Therapeutics

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Drug Profile

Research programme: antisense oligonucleotide therapies - NeuBase Therapeutics

Alternative Names: DM1 investigational genetic therapy; NT0100; NT0200

Latest Information Update: 28 Sep 2023

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At a glance

  • Originator NeuBase Therapeutics
  • Class Antisense DNA; Antisense oligonucleotides; Antisense RNA
  • Mechanism of Action RNA interference
  • Orphan Drug Status

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

    No
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Preclinical Myotonic dystrophy
  • No development reported Huntington's disease; Neurological disorders

Most Recent Events

  • 28 Sep 2023 No recent reports of development identified for preclinical development in Huntington's-disease in USA (SC)
  • 28 Sep 2023 No recent reports of development identified for preclinical development in Myotonic dystrophy in USA (SC)
  • 28 Feb 2023 No recent reports of development identified for research development in Neurological-disorders in USA (Parenteral)

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