Biogen Inc. (BIIB - Free Report) announced that its biosimilar version of AbbVie, Inc.’s (ABBV - Free Report) top-selling blockbuster drug, Humira has been approved by the European Commission. The biosimilar will be marketed by the trade name of Imraldi.
Imraldi (or SB5) will be used for a whole range of indications including rheumatoid arthritis, axial spondyloarthritis, ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitis, polyarticular juvenile idiopathic arthritis, active enthesitis-related arthritis, hidradenitis suppurativa and non-infectious uveitis.
We remind investors that the biosimilar was granted a positive opinion by the Committee for Medicinal Products for Human Use (CHMP) in June this year.
Biogen has a joint venture with Samsung BioLogics for biosimilars. Samsung Bioepis, the joint venture between the two companies, already marketsa couple of biosimilars in the EU – Flixabi (a biosimilar referencing J&J/Merck & Co., Inc.’s [(MRK - Free Report) ] Remicade) and Benepali (a biosimilar referencing Amgen/Pfizer’s Enbrel). This makes Imraldi the third anti-TNF biosimilar from Biogen to receive a marketing authorization in the EU.
Benepali is doing quite well, generating sales of $154 million in the first half of 2017 while Flixabi recorded sales of $2.5 million in the same period.
We note that earlier this year, Amgen, Inc. (AMGN - Free Report) gained EU approval for Amgevita, its biosimilar version of Humira.
Biogen’s shares have risen 0.6% this year so far while the industry recorded an increase of 7.9%.
Biogen carries a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
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