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ATA 200

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Drug Profile

ATA 200

Alternative Names: ATA-200; GNT-0007; LGMD-R5/LGMD2C gene therapy - Atamyo Therapeutics

Latest Information Update: 01 Apr 2024

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At a glance

  • Originator Atamyo Therapeutics
  • Class Gene therapies
  • Mechanism of Action Gene transference; Sarcoglycan replacements
  • Orphan Drug Status

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

    Yes - Limb girdle muscular dystrophies
  • New Molecular Entity No

Highest Development Phases

  • Preclinical Limb girdle muscular dystrophies

Most Recent Events

  • 26 Mar 2024 Italian Medicines Agency (AIFA) and French Medicines Agency (ANSM) approves a Clinical Trial Application (CTA) authorization for ATA 200 in Limb girdle muscular dystrophies in Italy and France respectively
  • 19 Sep 2023 Atamyo Therapeutics plans a phase Ib/II trial for Limb girdle muscular dystrophies (In children) in France and Italy (IV), in May 2024 (NCT05973630) (EudraCT-2023-506440-16-00)
  • 19 Sep 2023 Atmyo Therapeutics files a Clinical Trials application with the European Commission in Europe for Limb-girdle muscular dystrophy
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