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Eli Lilly CDR (CAD Hedged)

Eli Lilly CDR (CAD Hedged) logo
🇺🇸United States
Ownership
-
Employees
43K
Market Cap
$859.4B
Website
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

Active:1471
Completed:1717

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:1705
Phase 2:488
+3 more phases

Drug Approvals

91

SFDA:39
FDA:38
NMPA:13
+1 more agencies

Drug Approvals

Donanemab Injection

Product Name
记能达
Approval Number
国药准字SJ20240047
Approval Date
Dec 17, 2024
NMPA

Ixekizumab Injection

Product Name
拓咨
Approval Number
国药准字SJ20190034
Approval Date
Sep 10, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150284
Approval Date
Aug 6, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150285
Approval Date
Aug 6, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150287
Approval Date
Jun 27, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150286
Approval Date
Jun 27, 2024
NMPA

Ramucirumab Injection

Product Name
希冉择
Approval Number
国药准字SJ20220011
Approval Date
Mar 16, 2022
NMPA

Ramucirumab Injection

Product Name
希冉择
Approval Number
国药准字SJ20220012
Approval Date
Mar 16, 2022
NMPA

Ixekizumab Injection

Product Name
拓咨
Approval Number
S20190034
Approval Date
Aug 29, 2019
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
H20150287
Approval Date
Jul 3, 2019
NMPA
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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

Phase 1
1705 (56.4%)
Phase 3
602 (19.9%)
Phase 2
488 (16.1%)
Phase 4
175 (5.8%)
Not Applicable
53 (1.8%)
Early Phase 1
1 (0.0%)
phase_2_3
1 (0.0%)

A Study of LY4167586 in Participants With Obesity or Overweight Who Are Otherwise Healthy

Not Applicable
Not yet recruiting
Conditions
Overweight
Obesity
Interventions
Drug: LY4167586
Drug: 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

Not Applicable
Not yet recruiting
Conditions
Smoking
Interventions
Drug: Brenipatide
Drug: 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

and more 23 locations

Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease

Not Applicable
Not yet recruiting
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

and more 103 locations

A Study of Baricitinib (LY3009104) for the Delay of Stage 3 Type 1 Diabetes in At-Risk Children and Adults

Not Applicable
Not yet recruiting
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

and more 101 locations

A Study of Baricitinib (LY3009104) to Preserve Beta Cell Function in Children and Adults Newly Diagnosed With Type 1 Diabetes (BARICADE-PRESERVE)

Not Applicable
Not yet recruiting
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

and more 126 locations
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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.

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