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
- Prev
- 1
- 2
- Next
Clinical Trials
Distribution across different clinical trial phases (2988 trials with phase data)• Click on a phase to view related trials
A Study of LY3549492 in Chinese Participants With Type 2 Diabetes Mellitus
- First Posted Date
- 2025-07-18
- Last Posted Date
- 2025-07-18
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 36
- Registration Number
- NCT07073170
- Locations
- 🇨🇳
Peking University First Hospital, Dongcheng District, Beijing, China
🇨🇳West China Hospital of Sichuan University, Chengdu, Sichuan, China
🇨🇳Peking University People's Hospital, Beijing, China
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
- 2025-07-18
- Lead Sponsor
- Eli Lilly and Company
- Target Recruit Count
- 240
- Registration Number
- NCT07046923
- Locations
- 🇺🇸
The Ohio State University (OSU) Wexner Medical Center, Columbus, Ohio, United States
🇺🇸START Mountain Region, West Valley City, Utah, United States
🇺🇸Stanford Cancer Center, Stanford, California, 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
- Prev
- 1
- 2
- 3
- 4
- 5
- 393
- Next
News
IXICO Secures Full Data Rights to Landmark Bio-Hermes-002 Alzheimer's Study Through Strategic GAP Partnership
IXICO has deepened its collaboration with the Global Alzheimer's Platform Foundation through an agreement securing full data usage rights to the Bio-Hermes-002 study, one of the most prominent global studies in Alzheimer's disease research.
Eli Lilly Advances LOXO-435 in Phase 1 FORAGER-1 Study for FGFR3-Altered Advanced Cancers
Eli Lilly's FORAGER-1 Phase 1 study is evaluating LOXO-435 (LY3866288) as both monotherapy and combination treatment for locally advanced or metastatic solid tumors with FGFR3 gene alterations.
Livzon's Dual-Target IL-17A/F Antibody LZM012 Outperforms Secukinumab in Phase III Psoriasis Trial
Livzon Pharmaceutical's LZM012, the first domestic dual-target IL-17A/F monoclonal antibody, achieved superior efficacy compared to Secukinumab in a Phase III trial for moderate to severe plaque psoriasis.
Omega Funds Closes Oversubscribed $647M Fund VIII to Accelerate Life Sciences Innovation
Omega Funds successfully closed its eighth fund with $647 million in capital commitments, exceeding its $600 million target despite challenging fundraising conditions.
Bristol Myers Squibb and Pfizer Launch Direct-to-Patient Eliquis Program with 40% Price Discount
Bristol Myers Squibb and Pfizer announced a new direct-to-patient purchasing option for Eliquis (apixaban) through their Eliquis 360 Support program, offering eligible patients a cash price more than 40% below the current $606 list price.
FDA Implements Major Workforce Reduction and Policy Changes Amid Regulatory Overhaul
Up to 3,500 FDA staffers received termination notices following a Supreme Court ruling that found the government's HHS overhaul to be lawful.
Hengrui and Kailera's Dual GLP-1/GIP Obesity Drug Achieves 18% Weight Loss in Phase 3 Trial
Hengrui Pharma and Kailera Therapeutics' dual-acting obesity drug HRS9531 demonstrated 18% weight loss in a Phase 3 trial in China, significantly outperforming placebo by 16%.
Illimis Therapeutics Secures $42M Series B to Advance GAIA Platform for Alzheimer's and Immune Disease Treatments
Illimis Therapeutics closed a $42 million Series B funding round with participation from 18 investors to accelerate development of its GAIA platform targeting Alzheimer's disease and immune disorders.
Cipla Plans Entry into India's Weight Management Market as Obesity Becomes Strategic Priority
Cipla is preparing to enter India's weight management segment to address rising demand for effective obesity solutions, as announced by CEO Umang Vohra in the company's 2024-25 annual report.
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.