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Boehringer Ingelheim USA Corporation

🇺🇸United States
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

2.6k

Active:177
Completed:2074

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:1110
Phase 2:363
+3 more phases

Drug Approvals

92

PPB:51
SFDA:39
EMA:2

Drug Approvals

Synjardy

Authorization Status
Authorised
Approval Date
May 27, 2015
EMA

Synjardy

Authorization Status
Authorised
Approval Date
May 27, 2015
EMA

Clinical Trials

Distribution across different clinical trial phases (2077 trials with phase data)• Click on a phase to view related trials

Phase 1
1110 (53.4%)
Phase 3
446 (21.5%)
Phase 2
363 (17.5%)
Phase 4
134 (6.5%)
Not Applicable
22 (1.1%)
Early Phase 1
1 (0.0%)
phase_2_3
1 (0.0%)

A Study in Healthy People to Test How Itraconazole Influences the Amount of BI 3031185 in the Blood

Not Applicable
Not yet recruiting
Conditions
Healthy
Interventions
First Posted Date
2025-10-08
Last Posted Date
2025-10-08
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
14
Registration Number
NCT07211425
Locations
🇩🇪

Humanpharmakologisches Zentrum Biberach, Biberach, Germany

A Study to Test Whether Nerandomilast Can Help Slow Down Changes in the Lung in People With a Family History of Pulmonary Fibrosis

Not Applicable
Not yet recruiting
Conditions
Familial Pulmonary Fibrosis
Interstitial Lung Abnormalities
Interstitial Lung Diseases
Interventions
Drug: Placebo
First Posted Date
2025-10-01
Last Posted Date
2025-10-02
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
80
Registration Number
NCT07201922
Locations
🇺🇸

University of California Los Angeles, Los Angeles, California, United States

🇺🇸

University of Michigan Health System, Ann Arbor, Michigan, United States

🇫🇷

HOP Louis Pradel, Bron, France

and more 37 locations

Beamion LUNG-3: A Study to Test Whether Zongertinib Helps People With Surgically Removed, Non-small Cell Lung Cancer With HER2 Mutations Compared With Standard Treatment

Not Applicable
Not yet recruiting
Conditions
Non-small Cell Lung Cancer
Interventions
First Posted Date
2025-09-29
Last Posted Date
2025-10-07
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
400
Registration Number
NCT07195695
Locations
🇺🇸

Community Cancer Trials of Utah, Ogden, Utah, United States

🇺🇸

Premier Cancer Care, Fresno, California, United States

🇺🇸

University of California Los Angeles, Santa Monica, California, United States

and more 154 locations

A Study to Test How Well Different Doses of BI 1831169 in Combination With an Anti-PD1 Antibody Are Tolerated in Japanese People With Different Advanced Cancers

Not Applicable
Not yet recruiting
Conditions
Solid Tumors
Interventions
First Posted Date
2025-09-16
Last Posted Date
2025-09-16
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
46
Registration Number
NCT07176975
Locations
🇯🇵

National Cancer Center Hospital East, Chiba, Kashiwa, Japan

A Study in Healthy People to Test How 2 Different Formulations of a Combination Treatment (Vicadrostat and Empagliflozin) Are Taken up in the Body and How Food Influences the Amount of the Medicines in the Blood

Not Applicable
Recruiting
Conditions
Healthy
Interventions
Drug: vicadrostat / empagliflozin combination 1
Drug: vicadrostat / empagliflozin 2
First Posted Date
2025-08-21
Last Posted Date
2025-09-19
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
32
Registration Number
NCT07133399
Locations
🇩🇪

CRS Clinical Research Services Mannheim GmbH, Mannheim, Germany

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News

Boehringer Ingelheim Acquires First-in-Class Oncology Asset from Accent Therapeutics Targeting High ISG Expression Tumors

Boehringer Ingelheim has acquired a potentially first-in-class preclinical small molecule program from Accent Therapeutics targeting tumors with high interferon-stimulated gene (ISG) expression.

Qurient and Synaffix Partner to Develop First-in-Class CDK7 Dual-Payload ADC for Refractory Cancers

Qurient has signed a licensing agreement with Synaffix to develop a dual-payload ADC combining Qurient's CDK7 inhibitor mocaciclib with Synaffix's exatecan-based technology.

TegMine Therapeutics Partners with Boehringer Ingelheim to Develop Next-Generation ADCs Using Novel 2-Factor Antibody System

TegMine Therapeutics has entered a strategic research collaboration with Boehringer Ingelheim to develop safer, more selective antibody-drug conjugates using TegMine's proprietary 2-Factor Antibody System.

Roche Acquires 89bio for $3.5 Billion to Strengthen MASH Treatment Pipeline

Roche announced a definitive merger agreement to acquire 89bio for $14.50 per share in cash plus contingent value rights, totaling up to $3.5 billion.

UPC Court of Appeal Grants First Pharmaceutical Preliminary Injunction, Setting New Standard for Generic Drug Market Entry

The Unified Patent Court's Court of Appeal granted its first preliminary injunction in the pharmaceutical sector, blocking Zentiva from launching generic versions of Boehringer Ingelheim's Ofev across 17 European territories.

FDA Accepts First Non-Invasive Surrogate Endpoint for MASH Clinical Trials

The FDA has accepted Echosens' Letter of Intent to qualify liver stiffness measurement by FibroScan® as the first non-invasive surrogate endpoint for MASH clinical trials.

DAPA ACT HF-TIMI 68 Trial Shows Promise for In-Hospital SGLT2 Inhibitor Initiation Despite Missing Primary Endpoint

The DAPA ACT HF-TIMI 68 trial failed to show significant improvement in cardiovascular death or worsening heart failure when starting dapagliflozin during acute heart failure hospitalization, with 10.9% of treated patients versus 12.7% of placebo patients experiencing events at 60 days.

Controlled Release Drug Delivery Market Expands with Major Pharma Investment in Precision Medicine Technologies

Major pharmaceutical companies including AbbVie, AstraZeneca, and Merck are actively developing controlled drug release systems to enhance treatment of chronic diseases, cancer, and neurological disorders.

Boehringer Ingelheim Partners with AnGes for HGF Gene Therapy Manufacturing Ahead of FDA Filing

Boehringer Ingelheim has signed a contract development and manufacturing agreement with AnGes for the drug substance of their investigational hepatocyte growth factor gene therapy targeting peripheral arterial disease.

Molecular Partners Appoints Martin Steegmaier as Chief Scientific Officer to Advance DARPin Therapeutics Pipeline

Molecular Partners has appointed Martin Steegmaier, Ph.D. as Chief Scientific Officer effective October 1, 2025, bringing extensive oncology drug development experience from senior roles at Roche, MorphoSys, Boehringer Ingelberg, and SOTIO Biotech.

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