Lintuzumab Ac-225 - Actinium Pharmaceuticals

Drug Profile

Lintuzumab Ac-225 - Actinium Pharmaceuticals

Alternative Names: 225Ac-HuM-195; 225Ac-lintuzumab; AC225 MOAB M195; Ac225 monoclonal antibody M195; Actimab-A; Actimab-M; Actimab-MDS; Actinium-225 (225Ac)-Lintuzumab; Actinium-225-labelled HuM195; HuM195-Ac-225

Latest Information Update: 15 Mar 2018

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At a glance

  • Originator PDL BioPharma
  • Developer Actinium Pharmaceuticals; Baylor Research Institute; Memorial Sloan-Kettering Cancer Center; University of Texas M. D. Anderson Cancer Center
  • Class Antineoplastics; Immunoconjugates; Monoclonal antibodies; Radiopharmaceuticals
  • Mechanism of Action Ionising radiation emitters
  • Orphan Drug Status

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

    Yes - Acute myeloid leukaemia
  • New Molecular Entity No
  • Available For Licensing Yes - Cancer

Highest Development Phases

  • Phase II Acute myeloid leukaemia
  • Phase I Multiple myeloma

Most Recent Events

  • 13 Mar 2018 US FDA approves IND application for Lintuzumab Ac-225 in Acute myeloid leukaemia (Combination therapy, Second-line therapy or greater) in USA
  • 12 Feb 2018 Actinium Pharmaceuticals files an IND application with the FDA in USA for Acute myeloid leukaemia
  • 06 Feb 2018 Actinium Pharmaceuticals intends to file an IND application with the US FDA in USA for Myelodysplastic syndrome in the first half of 2018
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