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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:1479
Completed:1695

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:1703
Phase 2:488
+3 more phases

Drug Approvals

51

FDA:38
NMPA:13

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 (2987 trials with phase data)• Click on a phase to view related trials

Phase 1
1703 (57.0%)
Phase 3
602 (20.2%)
Phase 2
488 (16.3%)
Phase 4
175 (5.9%)
Not Applicable
17 (0.6%)
Early Phase 1
1 (0.0%)
phase_2_3
1 (0.0%)

A Study of Remternetug (LY3372993) in Healthy Participants

Not Applicable
Recruiting
Conditions
Healthy
Interventions
Drug: Remternetug (Test)
Drug: Remternetug (Reference)
First Posted Date
2025-07-09
Last Posted Date
2025-07-09
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
72
Registration Number
NCT07056309
Locations
🇺🇸

Fortrea Clinical Research Unit, Dallas, Texas, United States

🇺🇸

QPS Missouri, Springfield, Missouri, United States

A Study of LY4175408 in Participants With Advanced Cancer

Not Applicable
Not yet recruiting
Conditions
Neoplasm Metastasis
Triple Negative Breast Cancer
Carcinoma, Non-Small-Cell Lung
Small Cell Lung Carcinoma
Endometrial Neoplasms
Interventions
First Posted Date
2025-07-02
Last Posted Date
2025-07-02
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
240
Registration Number
NCT07046923
Locations
🇺🇸

Stanford Cancer Center, Stanford, California, United States

🇺🇸

Florida Cancer Specialists - Lake Nona - Sarah Cannon Research Institute, Orlando, Florida, United States

🇺🇸

Florida Cancer Specialists - Sarasota, Sarasota, Florida, United States

and more 18 locations

A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY4066708 in Healthy Participants

Not Applicable
Recruiting
Conditions
Healthy
Cancer
Interventions
Drug: LY4066708
Drug: Placebo
First Posted Date
2025-07-01
Last Posted Date
2025-07-01
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
104
Registration Number
NCT07046559
Locations
🇬🇧

Fortrea Clinical Research Unit, Holbeck, Leeds, United Kingdom

A Study of Multiple Olomorasib (LY3537982) Capsules in Healthy Participants

Not Applicable
Not yet recruiting
Conditions
Healthy
Interventions
First Posted Date
2025-06-29
Last Posted Date
2025-06-29
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
120
Registration Number
NCT07044271
Locations
🇺🇸

ICON Early Phase Services, San Antonio, Texas, United States

🇺🇸

ICON, Salt Lake City, Utah, United States

A Study of [14C]-LY4065967 in Healthy Participants

Phase 1
Not yet recruiting
Conditions
Healthy
Interventions
Radiation: [14C]-LY4065967 Oral
Radiation: [14C]-LY4065967 IV
First Posted Date
2025-06-26
Last Posted Date
2025-06-26
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
16
Registration Number
NCT07039045
Locations
🇺🇸

Fortrea Clinical Research Unit, Madison, Wisconsin, United States

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News

Empagliflozin Demonstrates Cost-Effectiveness in Chronic Kidney Disease Treatment, EMPA-KIDNEY Analysis Shows

A new analysis from the EMPA-KIDNEY trial demonstrates that empagliflozin is cost-effective for chronic kidney disease treatment, improving quality-adjusted life years while reducing healthcare costs.

BeyondSpring's Plinabulin Shows Promise in Reversing Checkpoint Inhibitor Resistance Through Dendritic Cell Activation

BeyondSpring's Plinabulin combined with radiation and PD-1 inhibitors achieved a 23% overall response rate and 54% disease control rate in patients who failed prior checkpoint inhibitor therapy.

Scottish Health Authority Approves Theramex's Abaloparatide for High-Risk Osteoporosis Treatment

The Scottish Medicines Consortium has recommended Theramex's Eladynos (abaloparatide) for treating osteoporosis in postmenopausal women at very high risk of fracture through NHS Scotland.

Biocon Races to Launch First Generic Semaglutide in Canada as Wegovy Patents Expire

Biocon Ltd. is seeking regulatory approval for generic versions of Novo Nordisk's Ozempic and Wegovy, targeting Canada as its first major market entry by 2026.

Protagonist Therapeutics Advances PN-477 Triple Agonist for Obesity Treatment, Targeting Same Mechanism as Eli Lilly's Retatrutide

Protagonist Therapeutics has selected PN-477, a novel triple agonist peptide targeting GLP-1, GIP, and GCG receptors, as a development candidate for obesity treatment with both oral and injectable formulations.

AbbVie Acquires In Vivo CAR-T Developer Capstan Therapeutics for Up to $2.1 Billion

AbbVie has agreed to acquire cell therapy developer Capstan Therapeutics in a deal worth up to $2.1 billion in cash, gaining access to innovative in vivo CAR-T technology.

Laverock Therapeutics Raises £20M in Expanded Seed Funding, Reports Positive Data for Cancer Cell Therapy Programs

Laverock Therapeutics has expanded its seed funding round to more than £20 million, with the latest £6.5 million extension led by Calculus Capital and including participation from Eli Lilly and Company.

Karnataka Government Seeks DCGI Investigation Into HCG Clinical Trial Ethics Violations

Karnataka's Health and Family Welfare Department has formally requested the Drug Controller General of India to investigate alleged ethical violations in clinical trials at HealthCare Global Enterprises Ltd (HCG) in Bengaluru.

Alzheimer's Drug Market Sees 780% Investment Surge Following Leqembi and Kisunla Approvals

Total M&A deal value in Alzheimer's disease jumped from $2 billion in 2022 to $18 billion in 2024, representing a 780% increase following the approval of disease-modifying treatments.

Longeveron Appoints Than Powell as Chief Business Officer to Lead Alzheimer's and HLHS Program Strategy

Longeveron Inc. has appointed Than Powell as Chief Business Officer effective July 7, 2025, to oversee partnering efforts for Alzheimer's disease and international strategy for hypoplastic left heart syndrome programs.

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