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Actoxumab/bezlotoxumab - Merck & Co

Drug Profile

Actoxumab/bezlotoxumab - Merck & Co

Alternative Names: 3D8; Bezlotoxumab/actoxumab; CDA-1/CDA-2; GS-CDA-1/MDX-1388; MBL-CDA1/MBL-CDB1; MDX-066 + MDX-1388; MDX-066/MDX-1388; MK-3415 + MK-6072; MK-3415/MK-6072; MK-3415A

Latest Information Update: 24 Jan 2018

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At a glance

  • Originator Medarex; University of Massachusetts Medical School
  • Developer Bristol-Myers Squibb; Merck & Co; University of Massachusetts Medical School
  • Class Antidiarrhoeals; Monoclonal antibodies
  • Mechanism of Action Bacterial toxin inhibitors
  • 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 Clostridium difficile infections

Most Recent Events

  • 24 Jan 2018 No recent reports on development identified - Phase-III for Clostridium difficile infections in Japan, Finland, Sweden, Poland, Greece, Belgium, Italy, Czech Republic, United Kingdom, Austria, Spain, Portugal, Denmark, Germany and USA (IV)
  • 20 Sep 2015 Merck announces intention to submit regulatory applications in USA, European Union and Canada in 2015
  • 20 Sep 2015 Efficacy and adverse events data from the phase III MODIFY I and II trials in Clostridium difficile infections released by Merck
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