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
32 drugs in development
By Therapeutic Area
top 6
R&D Momentum
88/100
Pipeline Velocity
71/100
Trial Completion Rate
91/100
Pipeline Concentration
20/100
Pipeline Freshness
75/100
Strategic Signals
Activity
Last 14 days
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
DAREON™-9: A Phase Ib Open-label Dose Escalation and Dose Confirmation Safety Study of Intravenous BI 764532 in Combination With a Single Agent Chemotherapy for the Treatment of Patients With Relapsed/Refractory Small Cell Lung Cancer After Platinum-based Chemotherapy
Open-label, Randomised, 4 Parallel-group, Phase I Clinical Trial to Investigate BI 456906 Occupancy of Glucagon Receptors in Liver and Glucagon-like Peptide 1 Receptors in Pancreas in Comparison With Semaglutide After Administration of Radiolabeled Tracer in Male and Female Subjects With Obesity Using PET and MRI
EASi-HF Reduced - A Phase III Double-blind, Randomised, Parallel-group Superiority Trial to Evaluate Efficacy and Safety of the Combined Use of Oral Vicadrostat (BI 690517) and Empagliflozin Compared With Placebo and Empagliflozin in Participants With Symptomatic Chronic Heart Failure (HF: NYHA II-IV) and Left Ventricular Ejection Fraction (LVEF) < 40%
A Phase II, Randomised, Double-blind, Parallel-group, 42-week Dose-finding Trial for BI 3034701 Administered Subcutaneously Compared to Placebo in Participants With Obesity or Overweight
A Randomised, Double-blind, Placebo-controlled Trial With an Open-label Extension to Assess the Pharmacokinetics, Safety, and Efficacy of Empagliflozin Tablets in Paediatric Patients With Chronic Kidney Disease (EMPA-KIDNEY® Kids)
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
An Open-label Extension Trial of the Long-term Safety and Efficacy of BI 1015550 Taken Orally in Patients With Idiopathic Pulmonary Fibrosis (IPF) and Progressive Pulmonary Fibrosis (PPF) (FIBRONEER™-ON)
EASi-PROTKT™ - A Phase III Double-blind, Randomised, Parallel-group Superiority Trial to Evaluate Efficacy and Safety of the Combined Use of Oral Vicadrostat (BI 690517) and Empagliflozin Compared With Placebo and Empagliflozin in Participants With Type 2 Diabetes, Hypertension and Established Cardiovascular Disease
A Multi-centre, Randomised, Placebo-controlled, Double-blind, Parallel-group Trial to Evaluate Safety and Efficacy of Spesolimab (BI 655130) in Adult Patients With Ulcerative Pyoderma Gangrenosum (PG) Who Require Systemic Therapy
DAREON™-5: An Open-label, Multi-center Phase II Dose Selection Trial of Intravenous BI 764532, a DLL3-targeting T Cell Engager, in Patients With Relapsed/Refractory Extensive-stage Small Cell Lung Cancer and in Patients With Other Relapsed/Refractory Neuroendocrine Carcinomas
Details
Company Overview
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Mkt Cap
$23.8B
Revenue
—
Cash
Therapeutic Focus
Pipeline
Regulatory
Pradaxa — PRADAXA
Application NDA022512 (NDA)
Mirapex — MIRAPEX ER
Application NDA022421 (NDA)
Tradjenta — TRADJENTA
Application NDA201280 (NDA)
Viramune — VIRAMUNE XR
Application NDA201152 (NDA)
Gilotrif — GILOTRIF
Application NDA201292 (NDA)
Jardiance — JARDIANCE
Application NDA204629 (NDA)
Striverdi Respimat — STRIVERDI RESPIMAT
Application NDA203108 (NDA)
Anjeso — VIVLODEX
Application NDA207233 (NDA)
PRAXBIND — PRAXBIND
Application BLA761025 (BLA)
Spiriva — SPIRIVA RESPIMAT
Application NDA021936 (NDA)
Anjeso — QMIIZ ODT
Application NDA211210 (NDA)
Anjeso — ANJESO
Application NDA210583 (NDA)
Pradaxa — PRADAXA
Application NDA214358 (NDA)
SPEVIGO — SPEVIGO
Application BLA761244 (BLA)
Catapres — ONYDA XR
Application NDA217645 (NDA)
Catapres — JAVADIN
Application NDA220256 (NDA)
Jascayd — JASCAYD
Application NDA218764 (NDA)
Hernexeos — HERNEXEOS
Application NDA219042 (NDA)
Anjeso — XIFYRM
Application NDA218395 (NDA)
Anjeso — QAMZOVA
Application NDA217593 (NDA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)