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
41 drugs in development
By Therapeutic Area
top 6
R&D Momentum
87/100
Pipeline Velocity
64/100
Trial Completion Rate
85/100
Pipeline Concentration
14/100
Pipeline Freshness
69/100
Strategic Signals
Activity
Last 14 days
A Phase 2, Multicenter, Open-label Study of Sotorasib (AMG 510) in Subjects With Stage IV NSCLC Whose Tumors Harbor a KRAS G12C Mutation in Need of First-line Treatment (CodeBreaK 201)
A Double-blind, Randomized, Placebo-controlled, Multicenter Study Assessing Olpasiran Use to Prevent First Major Cardiovascular Events in Participants With Elevated Lipoprotein(a)
A Phase 1/1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of AMG 410 Alone and in Combination With Other Agents in Participants With KRAS Altered Advanced or Metastatic Solid Tumors
A Phase 1/1b Study Evaluating the Safety, Tolerability, and Pharmacokinetics of AMG 436 as Monotherapy and in Combination With Other Therapies in Participants With Microsatellite Instability-high (MSI-H)/Mismatch Repair Deficient (dMMR) Solid Tumors
A Phase 3, Multicenter, Double-blind, Randomized Controlled Study Evaluating the Efficacy and Safety of Pegloticase Administered by Subcutaneous Injection Compared With Pegloticase Administered by Intravenous Injection, Both Administered Concurrently With Methotrexate Weekly, in Participants With Uncontrolled Gout
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, Open Label, Multicenter, Randomized Study of First Line Tarlatamab in Combination With Durvalumab, Carboplatin and Etoposide Versus Durvalumab, Carboplatin and Etoposide in Untreated Extensive Stage Small-Cell Lung Cancer (DeLLphi-312)
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Impact of Maridebart Cafraglutide on Cardiovascular Outcomes in Participants With Atherosclerotic Cardiovascular Disease and Overweight or Obesity
A Phase 1/2, Randomized, Double-Masked, Placebo-Controlled, Multicenter Study to Assess the Safety, Pharmacokinetics, and Efficacy of AMG 732 in Healthy Subjects and Subjects With Moderate-to-Severe Active Thyroid Eye Disease
A Phase 2 Open-label Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Inebilizumab in Children From 2 Years to Less Than 18 Years of Age With Generalized Myasthenia Gravis (gMG)
Phase 2a Study Evaluating the Efficacy, Safety, Tolerability and Pharmacokinetics of Tarlatamab in Chinese Subjects With Advanced Small Cell Lung Cancer After Two or More Prior Lines of Treatment (DeLLphi-307)
Details
Company Overview
$165.0B
Mkt Cap
$23.7B
Revenue
$12.0B
Cash
Therapeutic Focus
Recent SEC Filings
AMGEN INC (AMGN) (CIK 0000318154)
Pipeline
Regulatory
Sensipar — SENSIPAR
Application NDA021688 (NDA)
Vectibix — VECTIBIX
Application BLA125147 (BLA)
NPLATE — NPLATE
Application BLA125268 (BLA)
Prolia — PROLIA
Application BLA125320 (BLA)
Blincyto — BLINCYTO
Application BLA125557 (BLA)
Otezla — OTEZLA
Application NDA205437 (NDA)
Repatha — REPATHA
Application BLA125522 (BLA)
Corlanor — CORLANOR
Application NDA206143 (NDA)
MVASI — MVASI
Application BLA761028 (BLA)
Aimovig — AIMOVIG
Application BLA761077 (BLA)
Corlanor — CORLANOR
Application NDA209964 (NDA)
RIABNI — RIABNI
Application BLA761140 (BLA)
TEZSPIRE — TEZSPIRE
Application BLA761224 (BLA)
Tavneos — TAVNEOS
Application NDA214487 (NDA)
Lumakras — LUMAKRAS
Application NDA214665 (NDA)
Prolia — WYOST
Application BLA761362 (BLA)
Otezla — OTEZLA XR
Application NDA210745 (NDA)
Prolia — BILPREVDA
Application BLA761444 (BLA)
Prolia — CONEXXENCE
Application BLA761398 (BLA)
Prolia — OSPOMYV
Application BLA761392 (BLA)
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)