Leverkusen, North Rhine-Westphalia, Germany · Est. 1863 · 100,000 employees
Bayer is a multinational pharmaceutical and life sciences company focused on human and animal health, crop science, and consumer health products.
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 15 drugs with upcoming expirations
Pipeline
By Phase
29 drugs in development
By Therapeutic Area
top 6
R&D Momentum
85/100
Pipeline Velocity
64/100
Trial Completion Rate
92/100
Pipeline Concentration
37/100
Pipeline Freshness
76/100
Strategic Signals
Activity
Last 14 days
A Randomized, Double-blind, Placebo-controlled, Parallel Group Phase 2a Study With an Extension Phase to Evaluate the Efficacy and Safety of BAY 3401016 in Participants Aged 18 to 45 With Alport Syndrome
An 18-month, Open-label, Single-arm Safety Extension Study of an age-and Bodyweight-adjusted Oral Finerenone Regimen, in Addition to an ACEI or ARB, for the Treatment of Children and Young Adults From 1 to 18 Years of Age With Chronic Kidney Disease and Proteinuria
Open-label Study of Androgen Receptor Inhibition With dArolutamide Plus Androgen Deprivation Therapy (ADT) Versus ADT in Men With Metastatic Hormone-Sensitive Prostate Cancer Using an External Control Arm
A Prospective, Longitudinal, Multi-center, Observational Study of Acoramidis In Patients With Wild-type or Variant Transthyretin Amyloid Cardiomyopathy (ATTR-CM): MOSAIC-TTR Study
A First-in-human Study to Evaluate the Safety, Tolerability and Pharmacokinetics, Pharmacodynamics and Preliminary Clinical Activity of BAY 3713372, a Novel 2nd Generation PRMT5 Inhibitor, in Participants With MTAP-deleted Solid Tumors.
A Prospective, Single-arm, Phase 4 Study to Evaluate the Course of Serum Transthyretin (TTR) Level With Acoramidis in Adult Patients With Variant or Wild-type Transthyretin Amyloidosis With Cardiomyopathy (ATTR-CM) Previously Treated With Tafamidis
A Phase 3 Open-label, Randomized, Active-controlled, Multicenter Trial to Evaluate the Efficacy and Safety of Orally Administered BAY 2927088 Compared With Standard of Care as a First-line Therapy in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) With HER2-activating Mutations
Special Drug Investigation of Kovaltry in Hemophilia A Patients
A Placebo-controlled, Parallel-group, Double Blind, Randomized, Multi-cohort Phase 2 Study to Investigate Efficacy, Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of BAY 3670549 in Adult Participants With Atrial Fibrillation.
Details
Company Overview
$55.0B
Mkt Cap
$46.0B
Revenue
—
Cash
Therapeutic Focus
Pipeline
Regulatory
Kerendia — KERENDIA
Application NDA215341 (NDA)
Vitrakvi — VITRAKVI
Application NDA210861
Vitrakvi — VITRAKVI
Application NDA210861
Vitrakvi — VITRAKVI
Application NDA211710
Vitrakvi — VITRAKVI
Application NDA211710
Vitrakvi — VITRAKVI
Application NDA210861
Vitrakvi — VITRAKVI
Application NDA211710
Kerendia — KERENDIA
Application NDA215341
Vitrakvi — VITRAKVI
Application NDA210861
Vitrakvi — VITRAKVI
Application NDA211710
Hyrnuo — HYRNUO
Application NDA219972 (NDA)
Lynkuet — LYNKUET
Application NDA219469 (NDA)
Lotrimin — CLOTIC
Application NDA217628 (NDA)
Gyne-Lotrimin 3 Combination Pack — CLOTIC
Application NDA217628 (NDA)
Kerendia — KERENDIA
Application NDA215341
Vitrakvi — VITRAKVI
Application NDA210861
Vitrakvi — VITRAKVI
Application NDA211710
Stivarga — STIVARGA
Application NDA203085
Ambelvist — AMBELVIST
Application NDA219627 (NDA)
Stivarga — STIVARGA
Application NDA203085
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)