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Research programme: rare disease therapeutics - Spyre Therapeutics

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Drug Profile

Research programme: rare disease therapeutics - Spyre Therapeutics

Latest Information Update: 26 Dec 2023

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At a glance

  • Originator Aeglea Biotherapeutics
  • Developer Spyre Therapeutics
  • Class Enzymes; Recombinant proteins
  • Mechanism of Action Enzyme 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 Yes

Highest Development Phases

  • Research Unspecified

Most Recent Events

  • 29 Nov 2022 Early research in Unspecified in USA (unspecified route), prior to November 2022 (Aeglea BioTherapeutics pipeline, November 2022)

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