SANTA MONICA, Calif.--(BUSINESS WIRE)--GoodRx (NASDAQ: GDRX), a leading consumer-focused digital healthcare platform, today announced a collaboration with Biogen (NASDAQ: BIIB) that aims to improve the patient and healthcare provider (HCP) experience when initiating a new specialty therapy. HCPs who have decided to start patients with relapsing forms of multiple sclerosis (MS) on VUMERITY® (diroximel fumarate) may now find the enrollment form and submit to the specialty hub through Provider Mode. Announced today, GoodRx’s Provider Mode is a new experience built specifically for HCPs to help them access solutions for the medications they prescribe.
The SMC has approved VUMERITY (diroximel fumarate), a next-generation oral fumarate for the treatment of adults living with relapsing-remitting multiple sclerosis (RRMS). There are currently 15,000 people living with MS in Scotland.
The MHRA has granted marketing authorisation for diroximel fumarate as noral treatment for relapsing-remitting multiple sclerosis.
Biogen has announced that the European Commission (EC) has granted marketing authorisation for Vumerity® (diroximel fumarate) to treat adults with relapsing-remitting multiple sclerosis (MS).
CAMBRIDGE, Mass., Nov. 16, 2021 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) today announced that the European Commission (EC) has granted marketing authorization for VUMERITY®n(diroximel fumarate) to treat adults with relapsing-remitting multiple nsclerosis (MS). VUMERITY is a next-generation fumarate that offers the nconvenience of an oral medication with the established efficacy and nwell-characterized safety of TECFIDERA® (dimethyl fumarate). nGlobally, an estimated 2.8 million people live with MS, with more than 1nmillion people in Europe living with the disease.1,2
CAMBRIDGE, Mass., Oct. 13, 2021 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) today announced new data from its industry-leading portfolio of multiple sclerosis (MS) therapies. These data include additional results from the NOVA study on the efficacy of every six-week (Q6W) 300mg natalizumab intravenous (IV) administration, results from a comparative real-world evaluation of TYSABRI® (natalizumab) when compared to
The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended nine medicines including Biogen’s Vumerity (diroximel fumarate) and Roche’s Gavreto (pralsetinib) for approval.
Biogen Inc. (Nasdaq: BIIB) today announced that the Committee for Medicinal Products for Human Use (CHMP), part of the European Medicines Agency (EMA), issued a positive opinion and has recommended granting marketing authorization for VUMERITY® (diroximel fumarate) in the European Union (EU). VUMERITY is a next-generation oral fumarate for the treatment of adults with relapsing-remitting multiple sclerosis (RRMS). An estimated 2.8 million people live with MS across the globe, with some European countries demonstrating the highest prevalence of MS in the world.
Biogen’s Vumerity hit the market late last year, but eight months into the launch, the new multiple sclerosis drug is yet to take off.Biogen’s Vumerity hit the market late last year, but eight months into the launch, the new multiple sclerosis drug is yet to take off.
Alkermes plc has received a $150 million milestone payment from Biogen triggered by the U.S. FDA approval of VUMERITY (diroximel fumarate), a novel oral fumarate for the treatment of relapsing forms of multiple sclerosis, and Alkermes' transfer to Biogen.