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| Novo Nordisk receives positive opinion on recombinant factor XIII |
Novo Nordisk announced that the Committee for Medicinal Products for Human Use (CHMP) under the European Medicines Agency (EMA) adopted a positive opinion on the Company's recombinant factor XIII product (rFXIII). The Committee recommended marketing authorisation for rFXIII for once-monthly replacement therapy in patients from the age of six years with congenital factor XIII A-subunit deficiency.
rFXIII is a recombinant factor XIII product, and it is the only recombinant treatment option for congenital factor XIII A-subunit deficiency. Data have shown that rFXIII prevents bleeding and that it is well tolerated. "The development of rFXIII for a very small patient community with a serious bleeding disorder demonstrates our commitment to develop a broad and innovative pipeline of molecules to fulfil unmet medical needs within haemophilia and rare bleeding disorders," says Mads Krogsgaard Thomsen, executive vice president and chief science officer at Novo Nordisk. Novo Nordisk expects to receive the final marketing authorisation from the European Commission within approximately two months. Following the Commission’s approval, Novo Nordisk expects to launch rFXIII in Europe towards end of the year.
About Congenital factor XIII deficiency
About rFXIII rFXIII has also been filed for regulatory review with the FDA (U.S. Food and Drug Administration), Health Canada and SwissMedic.
About Novo Nordisk |




Novo Nordisk announced that the Committee for Medicinal Products for Human Use (CHMP) under the European Medicines Agency (EMA) adopted a positive opinion on the Company's recombinant factor XIII product (rFXIII). The Committee recommended marketing authorisation for rFXIII for once-monthly replacement therapy in patients from the age of six years with congenital factor XIII A-subunit deficiency.
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