CHMP adopts positive opinion of haemophilia B treatment, Alprolix
Posted: 26 February 2016 | | No comments yet
Alprolix is a recombinant clotting factor therapy developed for haemophilia B by fusing factor IX to the Fc portion of immunoglobulin G subclass 1…
Swedish Orphan Biovitrum (Sobi) and Biogen have received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommending that marketing authorisation be granted for Alprolix (rFIXFc) for the treatment of haemophilia B.
Alprolix is a recombinant clotting factor therapy developed for haemophilia B by fusing factor IX to the Fc portion of immunoglobulin G subclass 1, or IgG1 (a protein commonly found in the body). This enables Alprolix to use a naturally occurring pathway to prolong the time the therapy remains in the body. While Fc fusion has been used for more than 15 years, Sobi and Biogen are the first companies to utilise it in the treatment of haemophilia.
If approved, Alprolix would be among the first therapies in the European Union (EU) to offer people living with haemophilia B prolonged protection against bleeding episodes with prophylactic dosing intervals.
Seeing the benefits Fc fusion technology can offer
“This positive opinion marks an important step in our efforts to bring treatment innovation to people with haemophilia in Europe and around the world,” said Krassimir Mitchev, M.D., Ph.D., vice president and medical therapeutic area head of Haemophilia at Sobi. “We are already seeing the benefits that Fc fusion technology can offer through our recent EU launch of Elocta for people with haemophilia A. We are excited at the prospect of also offering the possibility for prolonged protection and reduced treatment burden to the haemophilia B community with Alprolix.”
The positive opinion was based on results from two global, Phase 3 clinical trials that demonstrated the efficacy, safety and pharmacokinetics of Alprolix for haemophilia B: the pivotal B-LONG study for previously treated adults and adolescents, and the Kids B-LONG study for previously treated children under age 12. The CHMP’s recommendation is now referred to the European Commission (EC), which grants marketing authorisation for medicines in the EU.
“Therapies that offer prolonged protection from bleeds are changing the way many approach treatment of haemophilia,” said Gilmore O’Neill, M.D., senior vice president, Drug Innovation Units at Biogen. “We are proud to work with Sobi to continue bringing to Europe these innovative Fc fusion therapies, which are grounded in the most robust real-world experience of any prolonged circulation factor therapies to date.”