Ingelheim am Rhein, Germany, Germany · Est. 1885 · 52,000 employees
Boehringer Ingelheim is a privately-held pharmaceutical company developing innovative medicines across respiratory, oncology, cardiovascular, and immunological therapeutic areas.
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 12 drugs with upcoming expirations
Pipeline
By Phase
18 drugs in development
By Therapeutic Area
top 5
R&D Momentum
89/100
Pipeline Velocity
74/100
Trial Completion Rate
91/100
Pipeline Concentration
43/100
Pipeline Freshness
77/100
Strategic Signals
Activity
Last 14 days
A Phase III Double-blind, Randomised, Placebo-controlled Trial to Evaluate Liver-related Clinical Outcomes and Safety of Once Weekly Injected Survodutide in Participants With Compensated Non-alcoholic Steatohepatitis/Metabolic Dysfunction Associated Steatohepatitis (NASH/MASH) Cirrhosis
A Double-blind, Randomised, Placebo-controlled, Parallel Group, Phase IIa Trial to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of BI 765423 Administered Intravenously With or Without Standard of Care in Patients With Idiopathic Pulmonary Fibrosis
A Phase III, Randomised, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of BI 1291583 2.5 mg Administered Once Daily for up to 76 Weeks in Patients With Bronchiectasis (The AIRTIVITY™ Study)
A Phase 3, Randomised, Double-blind, Parallel-group, Event-driven, Cardiovascular Safety Study With BI 456906 Administered Subcutaneously Compared With Placebo in Participants With Overweight or Obesity With Established Cardiovascular Disease (CVD) or Chronic Kidney Disease, and/or at Least Two Weight-related Complications or Risk Factors for CVD
A Randomised, Double-blind, Placebo-controlled, Multicentre, Phase III Trial Evaluating Long-term Efficacy and Safety of Survodutide Weekly Injections in Adult Participants With Noncirrhotic Non-alcoholic Steatohepatitis/Metabolic Dysfunction-associated Steatohepatitis (NASH/MASH) and (F2) - (F3) Stage of Liver Fibrosis
Beamion LUNG-3: A Randomized, Controlled, Multi-center Trial Evaluating Zongertinib as an Adjuvant Monotherapy Compared With Standard of Care in Patients With Early-stage, Resectable Non-small Cell Lung Cancer (Stage II-IIIB) Harboring Tyrosine Kinase Domain Activating HER2 Mutations
Randomised, Placebo-controlled, Double-blind, Parallel-group Phase II Study to Evaluate the Efficacy and Safety of Oral BI 3000202 in Patients With Moderate to Severe Systemic Lupus Erythematosus (SLE)
A Multicenter, International, Randomized, Double-blind, Placebo-controlled Clinical Trial of the Aldosterone Synthase Inhibitor BI 690517 in Combination With Empagliflozin in Patients With Chronic Kidney Disease
A Double-blind, Randomised, Placebo-controlled Trial Evaluating the Efficacy and Safety of Oral Nerandomilast Treatment in Patients With Systemic Sclerosis (SSc)
A Phase III, Randomised, Double-blind, Parallel-group, 56-week Study, Evaluating the Efficacy and Safety of Survodutide (BI 456906), Compared With Placebo, in Participants With Type 2 Diabetes, as an Adjunct to Diet and Physical Activity Alone or in Combination With Either Oral Antidiabetic Medications or Insulin
A Multicentre, Randomised, Double-blind, Parallel Group, Placebo-controlled Trial to Assess the Effects of Oral TRPC6 Inhibitor BI 764198 Taken Over a 104 Week Treatment Period in Adult and Adolescent Participants With Primary Focal Segmental Glomerulosclerosis (pFSGS) or Genetic FSGS Related to TRPC6 Gene Variants
PODOMOUNT-Basket, a Phase II, Multicentre, Randomised, 2-arm Parallel-group, Double-blind, Placebo-controlled Basket Trial to Assess Safety, Tolerability, PK, and Efficacy of BI 764198 in Four Proteinuric Kidney Diseases
Details
Company Overview
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Mkt Cap
$23.8B
Revenue
—
Cash
Therapeutic Focus
Pipeline
Regulatory
Spiriva — SPIRIVA
Application NDA021395
Spiriva — SPIRIVA RESPIMAT
Application NDA021936
Catapres — ONYDA XR
Application NDA217645 (NDA)
Spevigo — SPEVIGO
Application BLA761244
Ketalar — KETALAR
Application NDA016812
Catapres — JAVADIN
Application NDA220256 (NDA)
Spevigo — SPEVIGO
Application BLA761244
Jascayd — JASCAYD
Application NDA218764 (NDA)
Hernexeos — HERNEXEOS
Application NDA219042 (NDA)
Pradaxa — PRADAXA
Application NDA214358
Pradaxa — PRADAXA
Application NDA022512
Anjeso — XIFYRM
Application NDA218395 (NDA)
Vivlodex — XIFYRM
Application NDA218395 (NDA)
Spevigo — SPEVIGO
Application BLA761244
Spevigo — SPEVIGO
Application BLA761244
Anjeso — QAMZOVA
Application NDA217593 (NDA)
Vivlodex — QAMZOVA
Application NDA217593 (NDA)
Catapres — QLONILIK
Application NDA221094 (NDA)
Ketalar — KETALAR
Application NDA016812
Ketalar — KETALAR
Application NDA016812
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)