Eli Lilly CDR (CAD Hedged)

- Country
- 🇺🇸United States
- Ownership
- -
- Employees
- 43K
- Market Cap
- $859.4B
- Introduction
Eli Lilly & Co. engages in the discovery, development, manufacture, and sale of pharmaceutical products. The firm's products consist of diabetes, oncology, immunology, neuroscience, and other products and therapies. The company was founded by Eli Lilly in May 1876 and is headquartered in Indianapolis, IN.
Clinical Trials
3.5k
Trial Phases
6 Phases
Drug Approvals
91
Drug Approvals
Duloxetine Hydrochloride Enteric Capsules
- Product Name
- 欣百达
- Approval Number
- 国药准字HJ20150284
- Approval Date
- Aug 6, 2024
Duloxetine Hydrochloride Enteric Capsules
- Product Name
- 欣百达
- Approval Number
- 国药准字HJ20150285
- Approval Date
- Aug 6, 2024
Duloxetine Hydrochloride Enteric Capsules
- Product Name
- 欣百达
- Approval Number
- 国药准字HJ20150287
- Approval Date
- Jun 27, 2024
Duloxetine Hydrochloride Enteric Capsules
- Product Name
- 欣百达
- Approval Number
- 国药准字HJ20150286
- Approval Date
- Jun 27, 2024
Duloxetine Hydrochloride Enteric Capsules
- Product Name
- 欣百达
- Approval Number
- H20150287
- Approval Date
- Jul 3, 2019
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- 1
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Clinical Trials
Distribution across different clinical trial phases (3025 trials with phase data)• Click on a phase to view related trials
A Study of LY4167586 in Participants With Obesity or Overweight Who Are Otherwise Healthy
- Conditions
- OverweightObesity
- Interventions
- Drug: LY4167586Drug: Placebo
- First Posted Date
- 2025-11-06
- Last Posted Date
- 2025-11-06
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 84
- Registration Number
- NCT07225556
- Locations
- 🇺🇸
Fortrea Clinical Research Unit, Madison, Wisconsin, United States
🇸🇬Lilly Centre for Clinical Pharmacology, Singapore, Singapore
A Study of Brenipatide in Adults Who Quit Smoking Cigarettes and Want to Avoid Relapse
- Conditions
- Smoking
- Interventions
- Drug: BrenipatideDrug: Placebo
- First Posted Date
- 2025-11-03
- Last Posted Date
- 2025-11-04
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 222
- Registration Number
- NCT07223840
- Locations
- 🇺🇸
Coastal Carolina Research Center, North Charleston, South Carolina, United States
🇺🇸Circle Clinical Research, Sioux Falls, South Dakota, United States
🇺🇸Hillcrest Medical Research, DeLand, Florida, United States
Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease
- Conditions
- Peripheral Arterial Disease
- Interventions
- Drug: Placebo
- First Posted Date
- 2025-11-03
- Last Posted Date
- 2025-11-04
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 1205
- Registration Number
- NCT07223593
- Locations
- 🇺🇸
Floridian Clinical Research, LLC, Miami Lakes, Florida, United States
🇺🇸Deaconess Clinic- Gateway, Newburgh, Indiana, United States
🇺🇸Flourish Research - Bowie, Bowie, Maryland, United States
A Study of Baricitinib (LY3009104) for the Delay of Stage 3 Type 1 Diabetes in At-Risk Children and Adults
- Conditions
- Diabetes Mellitus, Type 1
- Interventions
- Drug: Placebo
- First Posted Date
- 2025-10-29
- Last Posted Date
- 2025-11-04
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 150
- Registration Number
- NCT07222137
- Locations
- 🇺🇸
Tallahassee Memorial HealthCare, Tallahassee, Florida, United States
🇺🇸University of South Florida, Tampa, Florida, United States
🇺🇸University of Iowa, Iowa City, Iowa, United States
A Study of Baricitinib (LY3009104) to Preserve Beta Cell Function in Children and Adults Newly Diagnosed With Type 1 Diabetes (BARICADE-PRESERVE)
- Conditions
- Diabetes Mellitus, Type 1
- Interventions
- Drug: Placebo
- First Posted Date
- 2025-10-29
- Last Posted Date
- 2025-11-04
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 300
- Registration Number
- NCT07222332
- Locations
- 🇺🇸
Barbara Davis Center for Childhood Diabetes, Aurora, Colorado, United States
🇺🇸Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania, United States
🇺🇸Driscoll Children's Hospital, Corpus Christi, Texas, United States
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- 1
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News
CMS Launches GENEROUS Model to Implement Most-Favored-Nation Pricing for Medicaid Prescription Drugs
The Centers for Medicare & Medicaid Services announced the GENEROUS Model, a voluntary pilot program launching in 2026 that will allow participating state Medicaid programs to purchase select drugs at prices aligned with those paid in other developed countries.
Foghorn Therapeutics Advances Multi-Target Protein Degrader Pipeline with FHD-909 Phase 1 Trial Progressing
Foghorn Therapeutics reported continued progress in its Phase 1 dose escalation trial of FHD-909 for SMARCA4-mutated cancers, primarily targeting non-small cell lung cancer patients.
AI Achieves Atomic Precision in Antibody Design, Revolutionizing Drug Discovery
Nobel Laureate David Baker's lab at the University of Washington has successfully used AI to design antibodies from scratch with atomic precision, compressing discovery timelines from years to weeks.
HRSA Approves Eight Drug Companies for 340B Rebate Model Pilot Program Starting January 2025
The Health Resources and Services Administration has approved eight pharmaceutical companies to participate in the 340B Rebate Model Pilot Program, which will begin on January 1, 2025.
Lilly Discontinues P2X7 Inhibitor LY3857210 for Chronic Pain After Phase II Failure
Eli Lilly has discontinued LY3857210, an oral P2X7 receptor inhibitor, after Phase II data failed to meet the company's internal success criteria for chronic pain treatment.
Eli Lilly's Tirzepatide Franchise Becomes World's Top-Selling Drug, Surpassing Keytruda
Eli Lilly's tirzepatide franchise, including Zepbound and Mounjaro, generated $10.1 billion in Q3 2024, overtaking Merck's Keytruda as the world's best-selling drug for the first time.
FDA Proposes Streamlined Approval Pathway to Accelerate Biosimilar Drug Development
The U.S. FDA released draft guidance proposing to reduce human clinical study requirements for certain biosimilar drugs and treat them more like generic medications to accelerate market availability.
Eli Lilly Partners with NVIDIA to Build Pharma's Most Powerful AI Supercomputer for Drug Discovery
Eli Lilly announced a partnership with NVIDIA to build what it claims will be the "most powerful supercomputer owned and operated by a pharmaceutical company" to accelerate drug discovery through artificial intelligence.
FDA Approves Simplified Single-Injection Maintenance Regimen for Lilly's Omvoh in Ulcerative Colitis
The FDA has approved a single-injection, once-monthly maintenance regimen for Omvoh (mirikizumab-mrkz) in adults with moderately to severely active ulcerative colitis, replacing the previous two-injection regimen.
Lilly Acquires Adverum Biotechnologies for $262M to Advance Gene Therapy for Wet AMD
Eli Lilly announced the acquisition of Adverum Biotechnologies for up to $261.7 million, including its lead gene therapy candidate Ixo-vec for wet age-related macular degeneration.
