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
22 drugs in development
By Therapeutic Area
top 6
R&D Momentum
73/100
Pipeline Velocity
41/100
Trial Completion Rate
75/100
Pipeline Concentration
20/100
Pipeline Freshness
74/100
Strategic Signals
Activity
Last 14 days
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 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)
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Felzartamab in Adults With IgA Nephropathy (PREVAIL)
Pediatric Patients With Spinal Muscular Atrophy in China: A Nationwide Registry
A Multicenter, Randomized, Dose-Blind, Phase 3 Long-Term Extension Study to Evaluate Continuous Safety and Efficacy of Litifilimab (BIIB059) in Adult Participants With Active Systemic Lupus Erythematosus
An Open-Label Long-Term Extension Study of Felzartamab in Participants With Antibody-Mediated Rejection or Microvascular Inflammation Previously Enrolled in TRANSCEND or TRANSPIRE
Prospective, Observational Survey Study Assessing Effectiveness of Zuranolone in Improving PPD Symptoms in the Real-world Setting
A Longitudinal Online Survey of Patient-Reported Changes in Postpartum Depression Symptoms Following Zuranolone Use
Details
Company Overview
$23.0B
Mkt Cap
$9.8B
Revenue
$2.3B
Cash
Therapeutic Focus
Recent SEC Filings
8-K
8-K
BIOGEN INC. (BIIB) (CIK 0000875045)
Pipeline
Regulatory
Spinraza — SPINRAZA
Application NDA209531
Tecfidera — TECFIDERA
Application NDA204063
Tecfidera — TECFIDERA
Application NDA204063
Tecfidera — TECFIDERA
Application NDA204063
Tecfidera — TECFIDERA
Application NDA204063
Tecfidera — TECFIDERA
Application NDA204063
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
Zurzuvae — ZURZUVAE
Application NDA217369
Spinraza — SPINRAZA
Application NDA209531
Spinraza — SPINRAZA
Application NDA209531
Tecfidera — TECFIDERA
Application NDA204063
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)