Clinical Trials
2.5k
Trial Phases
6 Phases
Drug Approvals
53
Clinical Trials
Distribution across different clinical trial phases (2068 trials with phase data)• Click on a phase to view related trials
A Study to Test How BI 1819479 is Taken up and Processed by the Body
- Conditions
- Healthy
- Interventions
- First Posted Date
- 2025-07-15
- Last Posted Date
- 2025-07-15
- Lead Sponsor
- Boehringer Ingelheim
- Target Recruit Count
- 14
- Registration Number
- NCT07065617
SGLT2 Inhibitors and Renal Anemia in Japan: RWD
- Conditions
- Chronic Kidney Disease
- Interventions
- Drug: SGLT2 inhibitor
- First Posted Date
- 2025-07-14
- Last Posted Date
- 2025-07-14
- Lead Sponsor
- Boehringer Ingelheim
- Target Recruit Count
- 15000
- Registration Number
- NCT07063316
- Locations
- 🇯🇵
Nippon Boehringer Ingelheim Co ., Ltd., Tokyo, Japan
A Study to Test Vicadrostat (BI 690517) Taken Together With Empagliflozin in People With Type 2 Diabetes, High Blood Pressure, and Cardiovascular Disease
- Conditions
- Diabetes Mellitus, Type 2HypertensionCardiovascular Diseases
- Interventions
- First Posted Date
- 2025-07-14
- Last Posted Date
- 2025-07-14
- Lead Sponsor
- Boehringer Ingelheim
- Target Recruit Count
- 11800
- Registration Number
- NCT07064473
- Locations
- 🇺🇸
Pinnacle Research Group, LLC, Anniston, Alabama, United States
🇺🇸Eastern Shore Research Group, Fairhope, Alabama, United States
🇺🇸The Institute for Liver Health, LLC, Chandler, Arizona, United States
Real-world Study to Describe the Effectiveness and Safety Outcomes of Jardiance in Chinese Patients With Heart Failure and Preserved Ejection Fraction
- Conditions
- Heart FailurePreserved Ejection Fraction
- First Posted Date
- 2025-07-02
- Last Posted Date
- 2025-07-02
- Lead Sponsor
- Boehringer Ingelheim
- Target Recruit Count
- 3000
- Registration Number
- NCT07047508
Real-world Comparative Effectiveness and Safety of Jardiance in Chinese Patients With Heart Failure of Reduced Ejection Fraction
- Conditions
- Heart Failure of Reduced Ejection Fraction (HFrEF)
- Interventions
- Drug: non-SGLT2 inhibitors
- First Posted Date
- 2025-07-01
- Last Posted Date
- 2025-07-01
- Lead Sponsor
- Boehringer Ingelheim
- Target Recruit Count
- 7500
- Registration Number
- NCT07044700
- Locations
- 🇨🇳
Fuwai Hospital; National Center for Cardiovascular Diseases, Beijing, China
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News
BioMed X and Servier Launch First European XSeed Labs to Advance AI-Driven Bispecific Antibody Design
BioMed X and Servier have launched the first XSeed Labs in Europe at the Spartners incubator in Paris-Saclay, implementing a crowdsourcing model that embeds academic researchers within pharmaceutical R&D facilities.
Oxford BioTherapeutics and Boehringer Ingelheim Advance Third Oncology Drug Candidate to IND-Enabling Studies
Oxford BioTherapeutics announced that Boehringer Ingelheim has selected a third drug candidate targeting OB33 to advance into IND-enabling studies under their ongoing collaboration.
Maxion Therapeutics Strengthens Leadership with Appointment of Dr. Stefan Härtle as Chief Development Officer
Maxion Therapeutics has appointed Dr. Stefan Härtle as Chief Development Officer, bringing nearly 20 years of pharmaceutical R&D experience to advance the company's KnotBody® platform into clinical trials.
Solu Therapeutics Appoints Enda Moran as COO to Scale CyTAC Platform Operations
Solu Therapeutics has appointed Enda Moran, PhD, MBA as Chief Operating Officer to lead operational functions as the company advances its Phase 1 clinical trial of STX-0712.
D&D Pharmatech's DD01 Shows Rapid Liver Fat Reduction in MASH Phase 2 Trial, Matching Competitor Results in Quarter of the Time
D&D Pharmatech's DD01 achieved 75.8% of patients with at least 30% liver fat reduction in just 12 weeks, matching Boehringer Ingelheim's servodutide results that required 48 weeks of treatment.
Major PBMs Exclude Humira Biosimilars from 2025 Formularies, Favor Private-Label Products
The three largest U.S. pharmacy benefit managers have excluded nearly all marketed Humira biosimilars from their 2025 standard formularies, marking a dramatic shift from 2024 when eight products were covered.
Saniona Advances Neurological Pipeline with Strategic Partnerships and Strong Financial Position
Saniona secured SEK 115 million through warrant exercise and maintains SEK 261 million in cash, strengthening its financial runway to advance three internal neurological programs to Phase 2 trials.
Ochre Bio Strengthens Leadership with Former Eli Lilly and AstraZeneca Executive as RNA Therapeutics Company Expands
Oxford-based Ochre Bio has appointed Dr. Elaine Sullivan, former VP at Eli Lilly and AstraZeneca, as Senior Independent Non-Executive Director to support the company's RNA therapeutics development for chronic liver disease.
Boehringer Ingelheim Reports Promising Results for SIRP Inhibitors in Cancer Immunotherapy Trials
Boehringer Ingelheim's SIRP inhibitor BI 765063, when combined with PD-1 inhibitor ezabenlimab and cetuximab, showed manageable safety and promising antitumor activity in patients with recurrent/metastatic head and neck cancer.
BioMed X and Boehringer Ingelheim Complete Groundbreaking Schizophrenia Research Project
BioMed X Institute and Boehringer Ingelheim have successfully completed their second neuroscience collaboration focused on schizophrenia, with Boehringer Ingelheim acquiring the research data for further development.