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 660Latest Information Update: 09 Dec 2025
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
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Orphan Drug Status
No
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- 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)