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
51
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
- Prev
- 1
- 2
- Next
Clinical Trials
Distribution across different clinical trial phases (2987 trials with phase data)• Click on a phase to view related trials
A Study of Remternetug (LY3372993) in Healthy Participants
- 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
- Conditions
- Neoplasm MetastasisTriple Negative Breast CancerCarcinoma, Non-Small-Cell LungSmall Cell Lung CarcinomaEndometrial 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
A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY4066708 in Healthy Participants
- Conditions
- HealthyCancer
- Interventions
- Drug: LY4066708Drug: 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
- 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
- Conditions
- Healthy
- Interventions
- 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
- Prev
- 1
- 2
- 3
- 4
- 5
- 393
- Next
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.