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GLM 101

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Drug Profile

GLM 101

Alternative Names: GLM-101

Latest Information Update: 24 Sep 2024

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At a glance

  • Originator Glycomine
  • Class Sugar phosphates
  • Mechanism of Action Mannose replacements
  • Orphan Drug Status

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

    Yes - Congenital disorder of glycosylation type 1A
  • New Molecular Entity Yes

Highest Development Phases

  • Phase II Congenital disorder of glycosylation type 1A

Most Recent Events

  • 18 Sep 2024 GLM 101 receives Fast Track designation for Congenital disorder of glycosylation type 1A [IV,Infusion] (In adolescents, In children, In infants, In neonates, In adults) in USA
  • 04 Mar 2024 Interim efficacy and adverse events data from phase II clinical trials in Congenital disorder of glycosylation type 1A released by Glycomine
  • 29 Nov 2022 Phase-II clinical trials in Congenital disorder of glycosylation type 1A (In adolescents, In adults, In children, In infants, In neonates) in USA (IV) (NCT05549219) (EudraCT2022-000565-40)

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