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Human plasma-derived fibrinolysin - Grifols

Drug Profile

Human plasma-derived fibrinolysin - Grifols

Alternative Names: BAY 57-9602; Fibrinolysin-human - Grifols; Plasmin - Grifols; TAL-05-00018

Latest Information Update: 02 Aug 2019

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At a glance

  • Originator Bayer
  • Developer Bausch & Lomb; Grifols
  • Class Serine endopeptidases; Thrombolytics
  • Mechanism of Action Plasmin stimulants
  • Orphan Drug Status

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

    Yes - Peripheral arterial occlusive disorders
  • New Molecular Entity Yes

Highest Development Phases

  • No development reported Peripheral arterial occlusive disorders; Stroke
  • Discontinued Eye disorders

Most Recent Events

  • 02 Aug 2019 No development reported - Phase-I/II for Stroke in United Kingdom, Germany, Slovakia, France, Austria, Spain, Serbia, Australia (Intra-arterial) (NCT01014975)
  • 02 Aug 2019 No development reported - Phase-II for Peripheral arterial occlusive disorders in Spain, Romania, Poland, Peru, India, USA, Germany, Czech Republic, Bulgaria, Slovakia, Serbia, Belgium (Intra-arterial) (NCT01222117)
  • 31 Jan 2016 Grifols Therapeutics completes phase II clinical trials in Peripheral arterial occlusive disorders in the US, Belgium, Bulgaria, Czech Republic, Germany, India, Peru, Poland, Romania, Serbia, Spain and Slovakia (Intra-arterial) (NCT01222117)
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