Thousand Oaks, CA, United States · Est. 1980 · 27,000 employees
One of the world's leading biotechnology companies.
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 5 drugs with upcoming expirations
Pipeline
By Phase
28 drugs in development
By Therapeutic Area
top 6
R&D Momentum
87/100
Pipeline Velocity
62/100
Trial Completion Rate
85/100
Pipeline Concentration
14/100
Pipeline Freshness
69/100
Strategic Signals
Activity
Last 14 days
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy and Living With Overweight or Obesity
A Phase 3, Randomized, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of Romiplostim Plus Predniso(lo)ne vs. Predniso(lo)ne Alone for the Treatment of Adults With Previously Untreated Primary Immune Thrombocytopenia (ITP).
A Randomized, Double-masked, Comparative Clinical Study Evaluating the Efficacy, Safety, and Immunogenicity of ABP 938 8 mg Versus EYLEA® HD (Aflibercept) Delivered Via Intravitreal Injection in Participants With Neovascular Age-related Macular Degeneration
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight
A Phase 3, Open-Label, Multicenter, Randomized Study of Subcutaneous vs Intravenous Tarlatamab in Participants With Relapsed Extensive-Stage Small Cell Lung Cancer After Platinum-based First-line Chemotherapy (DeLLphi-315)
A Phase 4, Randomized, Double-blind, Multicenter Non-inferiority Trial Evaluating the Efficacy and Safety of Intravenous KRYSTEXXA® (Pegloticase) Administered Every 4 Weeks Compared With KRYSTEXXA Administered Every 2 Weeks With Co-administration of Weekly Doses of Methotrexate, Followed by an Open-label Extension, in Participants With Uncontrolled Refractory Gout (FORWARD II)
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Maridebart Cafraglutide on Mortality and Morbidity in Participants Living With Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity (MARITIME-HF)
A Phase 1b, Open-label Study of Xaluritamig (AMG 509) in Adults With Metastatic Castration-resistant Prostate Cancer
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Dazodalibep in Participants With Sjögren's Syndrome With Moderate-to-severe Systemic Disease Activity
AMG 335 Expanded Access Program for IgG4-Related Disease
A Phase 3, Open-label, Multicenter, Randomized Study of Xaluritamig Plus Abiraterone Versus Investigator's Choice in Participants With Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer
Details
Company Overview
$165.0B
Mkt Cap
$23.7B
Revenue
$12.0B
Cash
Therapeutic Focus
Recent SEC Filings
8-K
8-K
AMGEN INC (AMGN) (CIK 0000318154)
Pipeline
Regulatory
Aimovig — AIMOVIG
Application BLA761077
Corlanor — CORLANOR
Application NDA209964 (NDA)
RIABNI — RIABNI
Application BLA761140 (BLA)
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
TEZSPIRE — TEZSPIRE
Application BLA761224 (BLA)
Tavneos — TAVNEOS
Application NDA214487 (NDA)
Tavneos — TAVNEOS
Application NDA214487
Lumakras — LUMAKRAS
Application NDA214665 (NDA)
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
Tavneos — TAVNEOS
Application NDA214487
Otezla — OTEZLA XR
Application NDA210745 (NDA)
Aimovig — AIMOVIG
Application BLA761077
Aimovig — AIMOVIG
Application BLA761077
8-K
Accession: 0000318154-26-000124
8-K
Accession: 0000318154-26-000119
AMGEN INC (AMGN) (CIK 0000318154)
Accession: 001-37702
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)