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BAYER AG

BAYER AG logo
🇩🇪Germany
Ownership
Public
Established
1863-08-01
Employees
99.7K
Market Cap
$30.1B
Website
http://www.bayer.com

Clinical Trials

2.6k

Active:863
Completed:1521

Trial Phases

5 Phases

Phase 1:1170
Phase 2:277
Phase 3:365
+2 more phases

Drug Approvals

280

CIMA_AEMPS:104
NMPA:61
SFDA:55
+2 more agencies

Drug Approvals

Aflibercept Intravitreous Injection

Product Name
艾力雅
Approval Number
国药准字SJ20255004
Approval Date
May 19, 2025
NMPA

Rivaroxaban Tablets

Product Name
拜瑞妥
Approval Number
国药准字HJ20181086
Approval Date
Nov 30, 2023
NMPA

Rivaroxaban Tablets

Product Name
拜瑞妥
Approval Number
国药准字HJ20181085
Approval Date
Nov 30, 2023
NMPA

Rivaroxaban Tablets

Product Name
拜瑞妥
Approval Number
国药准字HJ20181087
Approval Date
Nov 30, 2023
NMPA

Rivaroxaban Tablets

Product Name
拜瑞妥
Approval Number
国药准字HJ20181084
Approval Date
Nov 30, 2023
NMPA

Recombinant human interferon beta-1b for injection

Product Name
倍泰龙
Approval Number
国药准字SJ20130094
Approval Date
Aug 24, 2023
NMPA

Iloprost Solution for Inhalation

Product Name
万他维
Approval Number
国药准字HJ20140940
Approval Date
Apr 25, 2023
NMPA

Iloprost Solution for Inhalation

Product Name
万他维
Approval Number
国药准字HJ20140941
Approval Date
Apr 25, 2023
NMPA

Iloprost Solution for Inhalation

Product Name
万他维
Approval Number
国药准字HJ20140939
Approval Date
Apr 25, 2023
NMPA

Aflibercept Intravitreous Injection

Product Name
艾力雅
Approval Number
国药准字SJ20180010
Approval Date
Apr 10, 2023
NMPA
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Clinical Trials

Distribution across different clinical trial phases (2060 trials with phase data)• Click on a phase to view related trials

Phase 1
1170 (56.8%)
Phase 3
365 (17.7%)
Phase 2
277 (13.4%)
Phase 4
126 (6.1%)
Not Applicable
121 (5.9%)
phase_2_3
1 (0.0%)

BAY3401016; Biomarker Study Alport

Not Applicable
Not yet recruiting
Conditions
Alport Syndrome
Interventions
First Posted Date
2025-10-08
Last Posted Date
2025-10-08
Lead Sponsor
Bayer
Target Recruit Count
60
Registration Number
NCT07211685
Locations
🇺🇸

Nephrology Clinic at The Kirklin Clinic of UAB Hospital, Birmingham, Alabama, United States

🇺🇸

The Peggy and Harold Katz Family Drug Discovery Center - Nephrology, Miami, Florida, United States

🇺🇸

Center for Advanced Pediatrics - Nephrology, Atlanta, Georgia, United States

and more 57 locations

A Study to Learn More About How Safe Finerenone is, When it is Taken for a Longer Time With Standard Treatment, in Children and Young Adults With Heart Failure and Left Ventricular Systolic Dysfunction

Not Applicable
Not yet recruiting
Conditions
Left Ventricular Systolic Dysfunction
Heart Failure (Pediatric)
Interventions
First Posted Date
2025-09-25
Last Posted Date
2025-09-25
Lead Sponsor
Bayer
Target Recruit Count
117
Registration Number
NCT07192952
Locations
🇺🇸

Children's Hospital Colorado - Anschutz Medical Campus - Cardiology, Aurora, Colorado, United States

🇺🇸

Nemours Children's Hospital -Delaware, Wilmington, Delaware, United States

🇺🇸

UF Health Shands Hospital - Pediatric Cardiology, Gainesville, Florida, United States

and more 127 locations

A Study to Learn More About How Well Finerenone Works, How Safe it is, and How it Moves Into, Through, and Out of the Body Compared to Placebo When Taken With Standard Treatment in Children With Heart Failure and Left Ventricular Systolic Dysfunction

Not Applicable
Not yet recruiting
Conditions
Left Ventricular Systolic Dysfunction
Heart Failure (Pediatric)
Interventions
First Posted Date
2025-09-23
Last Posted Date
2025-09-23
Lead Sponsor
Bayer
Target Recruit Count
111
Registration Number
NCT07188805
Locations
🇺🇸

Children's Hospital Colorado - Anschutz Medical Campus - Cardiology, Aurora, Colorado, United States

🇺🇸

Nemours Children's Hospital -Delaware, Wilmington, Delaware, United States

🇺🇸

UF Health Shands Hospital - Pediatric Cardiology, Gainesville, Florida, United States

and more 129 locations

A Study to Assess the Safety and Effects of Different Doses of an Investigational Drug, BAY 3389934, in Healthy Japanese Volunteers.

Not Applicable
Recruiting
Conditions
Sepsis Associated Disseminated Intravascular Coagulation (DIC)
Interventions
Drug: Matching Placebo / Diluent
First Posted Date
2025-09-16
Last Posted Date
2025-10-03
Lead Sponsor
Bayer
Target Recruit Count
16
Registration Number
NCT07176728
Locations
🇯🇵

SOUSEIKAI Fukuoka Mirai Hospital, Fukuoka, Fukuoka Pref, Japan

An Observational Study to Learn More About the Safety of Rivaroxaban in Participants With Peripheral Arterial Disease Who Had Surgery to Improve Blood Flow to Their Legs

Active, not recruiting
Conditions
Peripheral Arterial Disease (PAD)
First Posted Date
2025-08-27
Last Posted Date
2025-10-08
Lead Sponsor
Bayer
Target Recruit Count
1500
Registration Number
NCT07142655
Locations
🇯🇵

Medical Data Vision Co., Ltd, Tokyo, Japan

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News

Irish Court Invalidates Bayer's Rivaroxaban Dosing Patent in €3.5 Billion Xarelto Challenge

The High Court of Ireland ruled that Bayer's patent protecting once-daily dosing of rivaroxaban (Xarelto) was invalid for lack of inventive step, affecting a product worth €3.5 billion globally in 2024.

Federal Circuit Upholds Generic Challenge to Bayer's Xarelto Patent Protection

The Federal Circuit rejected Bayer's appeal to dismiss a patent validity challenge from three generic drug makers targeting the blockbuster blood-thinning drug Xarelto.

Shilpa Medicare Receives EMA Approval for Generic Rivaroxaban Orodispersible Films

Shilpa Medicare Limited has secured European Medicine Agency approval for its generic Rivaroxaban Orodispersible Films, a bioequivalent alternative to Bayer's Xarelto tablets.

European Regulators Recommend Approval for Novo Nordisk's Weekly Diabetes Combination Therapy Kyinsu

The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended approval of Novo Nordisk's once-weekly injectable diabetes treatment Kyinsu for adults with type 2 diabetes.

Advanced Liver Cancer Pipeline Shows Robust Growth with 50+ Companies Developing Novel Therapies

DelveInsight's 2025 pipeline report reveals over 50 active companies developing 52+ advanced liver cancer therapies, indicating strong industry commitment to addressing this challenging malignancy.

Alnylam Pharmaceuticals Joins Alliance for Genomic Discovery to Accelerate RNAi Drug Development

Alnylam Pharmaceuticals has joined the Alliance for Genomic Discovery as the ninth member, gaining access to a comprehensive clinical genomic database containing 250,000 whole-genomes to accelerate RNA interference therapeutic development.

AskBio Completes Enrollment in Phase 1 Gene Therapy Trial for Rare Neurological Disease MSA-P

AskBio has completed enrollment of 11 participants in its Phase 1 REGENERATE MSA-101 trial testing AB-1005 gene therapy for multiple system atrophy-parkinsonian type (MSA-P), a rare neurodegenerative disease affecting approximately 400,000 people worldwide.

Berlin Center for Gene and Cell Therapies Breaks Ground, Creating European Hub for Advanced Therapeutics

Bayer AG, Charité – Universitätsmedizin Berlin, and the Berlin Institute of Health officially began construction of the Berlin Center for Gene and Cell Therapies in September 2025, marking a significant milestone in European biotechnology infrastructure.

Australian Court Denies Preliminary Injunction Against Sandoz Aflibercept Biosimilar Launch

The Federal Court of Australia denied Regeneron and Bayer's preliminary injunction application against Sandoz's aflibercept biosimilars, allowing the launch of Afqlir and Enzeevu to proceed as planned.

Roivant Sciences Gains Orphan Drug Designation in Japan for Mosliciguat in Pulmonary Hypertension

Roivant Sciences' subsidiary Pulmovant received orphan drug designation from Japan's Ministry of Health, Labour and Welfare for mosliciguat, an inhaled soluble guanylate cyclase activator.

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