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Research programme: mucopolysaccharidosis II therapy - Immusoft

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Drug Profile

Research programme: mucopolysaccharidosis II therapy - Immusoft

Alternative Names: Hunter syndrome therapy - Immusoft; MPS II therapy - Immusoft

Latest Information Update: 28 Sep 2024

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At a glance

  • Originator Immusoft
  • Class Cell therapies; Gene therapies
  • Mechanism of Action Cell replacements; Gene transference
  • Orphan Drug Status

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

    No
  • New Molecular Entity No

Highest Development Phases

  • No development reported Mucopolysaccharidosis II

Most Recent Events

  • 28 Sep 2024 No recent reports of development identified for preclinical development in Mucopolysaccharidosis-II in USA (Parenteral, Injection)
  • 26 Aug 2020 Preclinical trials in Mucopolysaccharidosis II in USA (Parenteral) (Immusoft pipeline, August 2020)
  • 05 Sep 2018 Immusoft receives SBIR grant from the National Institutes of Health for advancement of its B cell modification platform

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