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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:1475
Completed:1718

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 (3028 trials with phase data)• Click on a phase to view related trials

Phase 1
1705 (56.3%)
Phase 3
602 (19.9%)
Phase 2
488 (16.1%)
Phase 4
175 (5.8%)
Not Applicable
56 (1.8%)
Early Phase 1
1 (0.0%)
phase_2_3
1 (0.0%)

A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight

Not Applicable
Not yet recruiting
Conditions
Obesity
Overweight
Interventions
Drug: Placebo
First Posted Date
2025-11-18
Last Posted Date
2025-11-18
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
250
Registration Number
NCT07232719
Locations
🇺🇸

Artemis Institute for Clinical Research, Riverside, California, United States

🇺🇸

JEM Research Institute, Atlantis, Florida, United States

🇺🇸

Headlands Research Orlando, Orlando, Florida, United States

and more 29 locations

A Study of LY3549492 in Healthy Participants and Participants With Overweight or Obesity

Not Applicable
Recruiting
Conditions
Healthy
Obesity
Overweight
Interventions
First Posted Date
2025-11-18
Last Posted Date
2025-11-18
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
60
Registration Number
NCT07232732
Locations
🇺🇸

Fortrea Clinical Research Unit, Madison, Wisconsin, United States

A Study of LY4584180 in Adult Participants With Previously Treated Blood Cancers

Not Applicable
Not yet recruiting
Conditions
Lymphoma, Non-Hodgkin's
Lymphoma, Diffuse Large B-Cell
Follicular Lymphoma
Interventions
Drug: LY4584180
First Posted Date
2025-11-12
Last Posted Date
2025-11-14
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
360
Registration Number
NCT07226843
Locations
🇺🇸

City of Hope, Duarte, California, United States

🇺🇸

University of California, San Francisco (UCSF) - Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States

🇺🇸

University of Miami - Sylvester Cancer Center, Miami, Florida, United States

and more 6 locations

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

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
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News

Vanda's Tradipitant Reduces GLP-1 Induced Vomiting by 50% in Phase 2 Trial

Vanda Pharmaceuticals reported positive Phase 2 results showing tradipitant, an oral NK-1 receptor antagonist, reduced vomiting by 50% in patients receiving GLP-1 therapy for obesity.

Nxera Pharma Announces Strategic Restructuring with 15% Workforce Reduction to Focus on GPCR Pipeline

Nxera Pharma announced a focused restructuring plan targeting ≥JPY50 billion in net sales and ≥30% operating profit margin by 2030, with a 15% global workforce reduction affecting approximately 60 jobs.

Mangoceuticals Launches Direct Access Programs for Zepbound and Wegovy Through Eli Lilly and Novo Nordisk Partnerships

Mangoceuticals has launched MangoRx Direct and PeachesRx Direct programs providing direct access to FDA-approved GLP-1 medications Zepbound and Wegovy through partnerships with Eli Lilly and Novo Nordisk.

Gate Bioscience Raises $65 Million Series B to Advance Novel Oral Molecular Gate Therapies into Clinical Trials

Gate Bioscience closed a $65 million oversubscribed Series B financing led by Forbion, with participation from Eli Lilly and Company and existing investors, bringing total capital raised to $135 million.

Medicxi Closes €500M Fund V to Accelerate Asset-Centric Biotech Investments

Medicxi successfully raised €500 million ($581 million) for its sixth fund, demonstrating strong investor confidence in its asset-centric investment approach.

ABL Bio Secures $2.6 Billion Deal and $180 Million Strategic Investment from Eli Lilly for Grabbody Platform

ABL Bio signed a $2.6 billion technology transfer and joint development agreement with Eli Lilly for its Grabbody double antibody platform, marking one of the largest biotech deals in South Korea's history.

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.

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