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; and ALTEOGEN Inc. to develop subcutaneous (SC) formulations of biologics utilizing ALT-B4. The company was founded in 1978 and is headquartered in Cambridge, Massachusetts. Show more
225 Binney Street, Cambridge, MA, 02142, United States
Market Cap
26.97B
52 Wk Range
$110.04 - $202.41
Previous Close
$183.78
Open
$181.46
Volume
1,339,297
Day Range
$176.39 - $182.23
Enterprise Value
29.73B
Cash
3.816B
Avg Qtr Burn
N/A
Insider Ownership
0.17%
Institutional Own.
98.04%
Qtr Updated
12/31/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
Nusinersen (SPINRAZA) Details Spinal muscular atrophy | Approved Update | |
QALSODY™ BIIB067 (tofersen) Details Amyotrophic lateral sclerosis | Approved Update | |
Leqembi (Lecanemab) (Aβ mAb) 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 | |
ADUHELM™ / Aducanumab (Aβ mAb) Details Alzheimer’s disease | Approved Quarterly sales | |
Leqembi (Lecanemab) IV Maintenance Dosing Details Alzheimer's disease | Approved Quarterly sales | |
Leqembi (Lecanemab) SC formulation Details Alzheimer's disease | PDUFA Approval decision | |
Felzartamab Details Primary Membranous Nephropathy | Phase 3 Data readout | |
SKYCLARYS® (Omavaloxolone) Details Friedreich’s Ataxia | Phase 3 Data readout | |
Litifilimab (BIIB059) (BDCA2 Antibody) Details Cutaneous Lupus Erythematosus | Phase 3 Data readout | |
Zorevunersen Details Dravet Syndrome | Phase 3 Data readout | |
Dapirolizumab pegol Details Systemic lupus erythematosus | Phase 3 Update | |
Felzartamab Details Late antibody-mediated rejection in adult kidney transplant recipients | Phase 3 Update | |
Salanersen (BIIB115) (Antisense Oligonucleotide) Details Spinal Muscular Atrophy | Phase 3 Initiation | |
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 | |
BIIB074 (vixotrigine) Details no known indication | Failed Discontinued | |
ATXN2 ASO (BIIB105) Details Amyotrophic lateral sclerosis | Failed Discontinued | |
SB15 (biosimilar referencing EYLEA®) Details no known indication | Failed Discontinued |
