Cambridge, MA, United States · Est. 1978 · 7,500 employees
Pioneer in neuroscience, advancing innovative therapies.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 6 drugs with upcoming expirations
Pipeline
By Phase
21 drugs in development
By Therapeutic Area
top 6
R&D Momentum
74/100
Pipeline Velocity
45/100
Trial Completion Rate
75/100
Pipeline Concentration
20/100
Pipeline Freshness
73/100
Strategic Signals
Activity
Last 14 days
A Phase 3 Randomized, Placebo-Controlled Trial With a Longitudinal Natural History Run-In and Open-Label Extension to Evaluate BIIB067 Initiated in Clinically Presymptomatic Adults With a Confirmed Superoxide Dismutase 1 Mutation
An Open-Label Long-Term Extension Study of Felzartamab in Participants With Antibody-Mediated Rejection or Microvascular Inflammation Previously Enrolled in TRANSCEND or TRANSPIRE
A Double-Blind, Placebo-Controlled, Multicenter, Randomized Phase 2 Trial Evaluating the Efficacy and Safety of Felzartamab in Recipients of Kidney Transplants With Late Isolated Microvascular Inflammation (MVI)
A Phase 4 Study of Nusinersen (BIIB058) Among Patients With Spinal Muscular Atrophy Who Received Onasemnogene Abeparvovec
A Placebo-Controlled, Multicenter, Randomized Phase 2 Trial Evaluating the Efficacy and Safety of Felzartamab Compared to Placebo in Adult Participants With Graves' Disease
8-K
A Randomized, Double-Blind, Placebo-Controlled MAD Study With Open-Label Extension to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of BIIB147 Administered Intrathecally to Adult Participants With ALS
An Observational Study Utilising Data From Big MS Data Registries to Evaluate the Long-Term Safety of Vumerity and Tecfidera
A Multicenter, Observational, Postmarketing Surveillance Study of Spinraza Injection (Nusinersen Sodium) When Used in Routine Medical Practice in Korea
A Randomized, Blinded, Placebo-Controlled, Phase 1 Single Ascending Dose Study in Healthy Adult Male Volunteers and an Open-Label Multiple Ascending Dose Study With Long-Term Extension in Pediatric SMA Participants Previously Treated With Onasemnogene Abeparvovec (Zolgensma™) to Evaluate the Safety, Tolerability, and Pharmacokinetics of BIIB115
A 2-Part Seamless Part A (Phase 2)/Part B (Phase 3) Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of BIIB059 in Participants With Active Subacute Cutaneous Lupus Erythematosus and/or Chronic Cutaneous Lupus Erythematosus With or Without Systemic Manifestations and Refractory and/or Intolerant to Antimalarial Therapy (AMETHYST)
An Open-Label Study to Assess the Efficacy and Safety of Multiple Doses of Salanersen (BIIB115) Delivered Intrathecally to Treatment-Naïve, Presymptomatic Infants With Genetically Diagnosed Spinal Muscular Atrophy
Details
Company Overview
$23.0B
Mkt Cap
$9.8B
Revenue
$2.3B
Cash
Therapeutic Focus
Recent SEC Filings
8-K
8-K
8-K
BIOGEN INC. (BIIB) (CIK 0000875045)
Pipeline
Regulatory
Vumerity — VUMERITY
Application NDA211855
Vumerity — VUMERITY
Application NDA211855
Vumerity — VUMERITY
Application NDA211855
Tecfidera — TECFIDERA
Application NDA204063
Zurzuvae — ZURZUVAE
Application NDA217369 (NDA)
Zurzuvae — ZURZUVAE
Application NDA217369
Qalsody — QALSODY
Application NDA215887 (NDA)
Qalsody — QALSODY
Application NDA215887
Skyclarys — SKYCLARYS
Application NDA216718 (NDA)
Spinraza — SPINRAZA
Application NDA209531
Tecfidera — TECFIDERA
Application NDA204063
Vumerity — VUMERITY
Application NDA211855
Vumerity — VUMERITY
Application NDA211855
Zurzuvae — ZURZUVAE
Application NDA217369
Spinraza — SPINRAZA
Application NDA209531
Spinraza — SPINRAZA
Application NDA209531
Vumerity — VUMERITY
Application NDA211855
Tecfidera — TECFIDERA
Application NDA204063
8-K
Accession: 0000875045-26-000094
8-K
Accession: 0000875045-26-000073
8-K
Accession: 0000875045-26-000068
Zurzuvae — ZURZUVAE
Application NDA217369
BIOGEN INC. (BIIB) (CIK 0000875045)
Accession: 000-19311
Spinraza — SPINRAZA
Application NDA209531
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)