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Eli Lilly and Co

🇺🇸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.

Study for Participants With Advanced, Not Amenable to Surgery, or Metastatic Lung Cancer Comparing Treatment With Pemetrexed + Cisplatin + Enzastaurin Versus Pemetrexed + Cisplatin + Placebo

Phase 2
Terminated
Conditions
Lung Cancer
Interventions
First Posted Date
2007-10-03
Last Posted Date
2020-11-05
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
35
Registration Number
NCT00538681
Locations
🇷🇴

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bucharest, Romania

Trial of Paclitaxel, Bevacizumab, and Enzastaurin Versus Paclitaxel, Bevacizumab and Placebo for Breast Cancer

Phase 2
Terminated
Conditions
Breast Cancer
Interventions
First Posted Date
2007-09-28
Last Posted Date
2020-09-24
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
2
Registration Number
NCT00536939
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Omaha, Nebraska, United States

A Study Comparing Duloxetine and Placebo in Assessing Energy and Vitality in Major Depressive Disorder (MDD) Patients

Phase 4
Completed
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2007-09-27
Last Posted Date
2009-11-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
776
Registration Number
NCT00536471
Locations
🇵🇷

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Juan, Puerto Rico

Study of Pemetrexed + Carboplatin + Bevacizumab + Enzastaurin Versus Pemetrexed + Carboplatin + Bevacizumab + Placebo in Participants With Non-Small Cell Lung Cancer Who Have Not Been Previously Treated With Chemotherapy

Phase 2
Completed
Conditions
Non-small Cell Lung Cancer
Interventions
First Posted Date
2007-09-21
Last Posted Date
2021-05-13
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
40
Registration Number
NCT00533429
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Omaha, Nebraska, United States

Duloxetine - Warfarin Pharmacodynamic Study

Phase 1
Completed
Conditions
Anticoagulant Effect of Warfarin When Taken With Duloxetine.
Interventions
First Posted Date
2007-09-21
Last Posted Date
2008-10-02
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
60
Registration Number
NCT00533026
Locations
🇬🇧

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559), Mon - Fri, 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician, Leeds, West Yorkshire, United Kingdom

A Study of IMC-1121B (Ramucirumab) With or Without Dacarbazine in Metastatic Malignant Melanoma

Phase 2
Completed
Conditions
Metastatic Malignant Melanoma
Interventions
Biological: IMC-1121B (ramucirumab)
Drug: Dacarbazine
First Posted Date
2007-09-21
Last Posted Date
2014-08-01
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
106
Registration Number
NCT00533702
Locations
🇺🇸

ImClone Investigational Site, Seattle, Washington, United States

Carotid Artery Intima-Media Thickness Following Exposure to Raloxifene or Placebo

Phase 4
Completed
Conditions
Osteoporosis, Post-Menopausal
Interventions
Drug: raloxifene
Drug: Placebo
First Posted Date
2007-09-20
Last Posted Date
2007-09-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
147
Registration Number
NCT00532246
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Walnut Creek, California, United States

Study of Teriparatide in the Treatment of Postmenopausal Women With Osteoporosis

Phase 3
Completed
Conditions
Osteoporosis, Post-Menopausal
Interventions
First Posted Date
2007-09-20
Last Posted Date
2007-09-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
50
Registration Number
NCT00532207
Locations
🇷🇺

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Moscow, Russian Federation

Bone Marker Changes With Teriparatide/Postmenopausal Osteoporosis

Phase 4
Completed
Conditions
Osteoporosis, Post-Menopausal
Interventions
First Posted Date
2007-09-20
Last Posted Date
2007-09-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
45
Registration Number
NCT00532545
Locations
🇵🇷

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Juan, Puerto Rico

Long Term Effects of Raloxifene Treatment on Bone Quality

Phase 4
Completed
Conditions
Osteoporosis, Post-Menopausal
Interventions
Drug: Raloxifene
Drug: Placebo
First Posted Date
2007-09-20
Last Posted Date
2007-09-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
31
Registration Number
NCT00532428
Locations
🇪🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Oviedo, Spain

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