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Rurioctocog alfa pegol - Takeda

Drug Profile

Rurioctocog alfa pegol - Takeda

Alternative Names: Adynovate; Adynovi; BAX-855; EHL rFVIII PEG; Extended half-life recombinant FVIII; Full-length longer-acting rFVIII; LA rFVIII PEG; PEG factor VIII; PEGylated recombinant factor VIII; PEGylated rFVIII; SHP-660; TAK 660

Latest Information Update: 09 Dec 2025

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At a glance

  • Originator Baxter International; Nektar Therapeutics
  • Developer Baxter International; Nektar Therapeutics; Takeda
  • Class Antihaemorrhagics; Blood coagulation factors; Coagulants; Polyethylene glycols; Recombinant proteins
  • Mechanism of Action Factor VIII replacements
  • 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

  • Marketed Haemophilia A

Most Recent Events

  • 31 Jul 2025 Preregistration for Haemophilia A in China (IV) (Takeda pipeline, November 2025)
  • 29 Oct 2024 Takeda completes a phase III trial in Haemophilia A (In children, In infants, In neonates, Treatment-naive) in USA, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Hungary, Italy, South Korea, Spain, Malaysia, Norway, Singapore, Taiwan, Thailand, Turkey, Ukraine, United Kingdom, Netherlands (IV) (NCT02615691)
  • 05 Sep 2024 Takeda completes a phase III trial for Haemophilia A (In children, In adolescents, In adults, Treatment-experienced, Prevention) in China (IV) (NCT05707351)

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