Programmed cellular immunotherapeutic - Fate Therapeutics

Drug Profile

Programmed cellular immunotherapeutic - Fate Therapeutics

Alternative Names: FT1050/FT4145 - modulated mobilised peripheral blood; Programmed mobilised peripheral blood; ProTmune; ProTmune FT1050/FT4145 programmed mobilised peripheral blood

Latest Information Update: 19 Sep 2017

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At a glance

  • Originator The Scripps Research Institute
  • Developer Fate Therapeutics
  • Class Cell therapies
  • Mechanism of Action Immunomodulators
  • Orphan Drug Status

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

    Yes - Graft-versus-host disease
  • New Molecular Entity No

Highest Development Phases

  • Phase II Cytomegalovirus infections; Graft-versus-host disease

Most Recent Events

  • 18 Sep 2017 Phase-II clinical trials in Graft-versus-host disease and Cytomegalovirus infections (Prevention) in USA
  • 07 Oct 2016 Fate Theraeputics receives patent allowance for Programmed cellular immunotherapeutic in USA
  • 01 Oct 2016 Programmed cellular immunotherapeutic - Fate Therapeutics receives Orphan Drug status for Graft-versus-host disease (Prevention) in Europe
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