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Efzimfotase alfa - Alexion AstraZeneca Rare Disease

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Drug Profile

Efzimfotase alfa - Alexion AstraZeneca Rare Disease

Alternative Names: ALXN-1850

Latest Information Update: 28 Aug 2024

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At a glance

  • Originator Alexion Pharmaceuticals
  • Developer Alexion AstraZeneca Rare Disease
  • Class Recombinant fusion proteins
  • Mechanism of Action Alkaline phosphatase stimulants
  • 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

  • Phase III Hypophosphatasia

Most Recent Events

  • 28 Aug 2024 No recent reports of development identified for phase-I development in Hypophosphatasia in USA (IV, Infusion)
  • 28 Aug 2024 No recent reports of development identified for phase-I development in Hypophosphatasia in USA (SC, Injection)
  • 24 Jul 2024 Alexion AstraZeneca Rare Disease intends to submit a regulatory application for Hypophosphatasia in 2025

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