Biogen Inc. discovers, develops, manufactures, and delivers therapies in the United States, Europe, Germany, Asia, and internationally. The company provides TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, and TYSABRI for multiple sclerosis (MS); SPINRAZA for spinal muscular atrophy; SKYCLARYS to treat Friedreich's Ataxia; QALSODY for treating amyotrophic lateral sclerosis; FUMADERM to treat plaque psoriasis; BENEPALI, an etanercept biosimilar referencing ENBREL; IMRALDI, an adalimumab biosimilar referencing HUMIRA; FLIXABI, an infliximab biosimilar referencing REMICADE. It offers LEQEMBI for the treatment of Alzheimer's disease; ZURZUVAE for the treatment of postpartum depression; RITUXAN to treat non-Hodgkin's lymphoma, chronic lymphocytic leukemia (CLL), rheumatoid arthritis, two forms of ANCA-associated vasculitis, and pemphigus vulgaris; RITUXAN HYCELA for non-Hodgkin's lymphoma and CLL; GAZYVA to treat CLL and follicular lymphoma; OCREVUS for relapsing MS and primary progressive MS; LUNSUMIO to treat relapsed or refractory follicular lymphoma; glofitamab for aRelapsed or refractory diffuse large B-cell lymphoma; and other anti-CD20 therapies. Biogen Inc. has collaboration and license agreements with Merz Therapeutics; Alkermes Pharma Ireland Limited; Denali Therapeutics Inc.; UCB; Eisai Co., Ltd.; Genentech, Inc.; Neurimmune SubOne AG; Ionis Pharmaceuticals, Inc.; Samsung Bioepis; and Sage Therapeutics, Inc., as well as collaborations with Stoke Therapeutics, Inc. for the development and commercialization of zorevunersen, a disease modifying medicine for the treatment of Dravet syndrome; Dayra Therapeutics, Inc. to develop oral macrocyclic peptides; Vanqua Bio, Inc. for developing Vanqua's preclinical oral C5aR1 antagonist compound; City Therapeutics, Inc. to develop select novel RNAi therapies. The company was founded in 1978 and is headquartered in Cambridge, Massachusetts. Show more
225 Binney Street, Cambridge, MA, 02142, United States
Market Cap
28.81B
52 Wk Range
$110.04 - $202.41
Previous Close
$196.34
Open
$196.03
Volume
709,349
Day Range
$194.43 - $198.72
Enterprise Value
28.45B
Cash
3.816B
Avg Qtr Burn
N/A
Insider Ownership
0.26%
Institutional Own.
97.84%
Qtr Updated
12/31/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
QALSODY™ BIIB067 (tofersen) Details Amyotrophic lateral sclerosis | Approved Update | |
ADUHELM™ / Aducanumab (Aβ mAb) Details Alzheimer’s disease | Approved Quarterly sales | |
Leqembi (Lecanemab) (Aβ mAb) Details Alzheimer's disease | Approved Quarterly sales | |
Leqembi (Lecanemab) IV Maintenance Dosing Details Alzheimer's disease | Approved Quarterly sales | |
SKYCLARYS™ (Omavaloxolone) Details Friedreich’s Ataxia | Approved Quarterly sales | |
ZURZUVAE BIIB125 (zuranolone) Details Postpartum depression | Approved Quarterly sales | |
TOFIDENCE (BIIB800) (tocilizumab) Details Polyarticular juvenile idiopathic arthritis, Rheumatoid arthritis | Approved Quarterly sales | |
Leqembi (Lecanemab) SC formulation Details Alzheimer's disease | PDUFA Approval decision | |
Nusinersen (SPINRAZA) Details Spinal muscular atrophy | PDUFA Approval decision | |
SKYCLARYS® (Omavaloxolone) Details Friedreich’s Ataxia | Phase 3 Data readout | |
Felzartamab Details Primary Membranous Nephropathy | Phase 3 Data readout | |
Litifilimab (BIIB059) (BDCA2 Antibody) Details Cutaneous Lupus Erythematosus | Phase 3 Data readout | |
Zorevunersen Details Dravet Syndrome | Phase 3 Data readout | |
Felzartamab Details Late antibody-mediated rejection in adult kidney transplant recipients | Phase 3 Update | |
Dapirolizumab pegol Details Systemic lupus erythematosus | Phase 3 Update | |
BIIB124 Details Essential tremor | Phase 2b Data readout | |
BIIB080 (tau ASO) Details Alzheimer's disease | Phase 2 Data readout | |
IONS582 /BIIB121 Details Angelman Syndrome | Phase 1b Data readout | |
BIIB113 Details Alzheimer's disease | Phase 1 Update | |
BIIB093 (IV glibenclamide) Details Acute myocardial infarction | Failed Discontinued | |
ATXN2 ASO (BIIB105) Details Amyotrophic lateral sclerosis | Failed Discontinued | |
BIIB074 (vixotrigine) Details no known indication | Failed Discontinued | |
SB15 (biosimilar referencing EYLEA®) Details no known indication | Failed Discontinued |
