- Trials with a EudraCT protocol (1,061)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,061 result(s) found for: eli lilly.
Displaying page 16 of 54.
| EudraCT Number: 2011-005217-37 | Sponsor Protocol Number: I4O-MC-BACC(b) | Start Date*: 2012-08-22 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Assessment of Safety, Tolerability, and Pharmacodynamic Effects of LY2886721 in Patients with Mild Cognitive Impairment Due to Alzheimer’s Disease or Mild Alzheimer's Disease | |||||||||||||
| Medical condition: Mild Cognitive Impairment Due to Alzheimer’s Disease or Mild Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001473-24 | Sponsor Protocol Number: F3Z-MC-IOQL | Start Date*: 2014-02-05 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: An Individualized treatMent aPproach for oldER patIents: A randomized, controlled stUdy in type 2 diabetes Mellitus | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003552-21 | Sponsor Protocol Number: I7I-MC-XNAA | Start Date*: 2014-05-27 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Comparison of the Oxyntomodulin Analog, LY2944876, to Once-Weekly Exenatide and to Placebo in Patients with Type 2 Diabetes. | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) PL (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005273-47 | Sponsor Protocol Number: I8F-MC-GPIG | Start Date*: 2022-11-21 | ||||||||||||||||
| Sponsor Name:Eli Lilly and Company | ||||||||||||||||||
| Full Title: Tirzepatide Study of Renal Function in People with Overweight or Obesity and Chronic Kidney Disease with or without Type 2 Diabetes: Focus on Kidney Hypoxia in Relation to Fatty Kidney Disease usin... | ||||||||||||||||||
| Medical condition: Obesity and Chronic Kidney disease | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) DK (Trial now transitioned) AT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-000077-25 | Sponsor Protocol Number: I5T-MC-AACI | Start Date*: 2020-07-13 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Assessment of Safety, Tolerability, and Efficacy of Donanemab in Early Symptomatic Alzheimer’s Disease | |||||||||||||
| Medical condition: Early Symptomatic Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) NL (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002933-12 | Sponsor Protocol Number: DRM06-AD05 | Start Date*: 2020-10-12 | |||||||||||
| Sponsor Name:Dermira, a wholly owned subsidiary of Eli Lilly and Company | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF LEBRIKIZUMAB IN PATIENTS WITH MODERATE-TO-SEVERE ATOPIC DERMATITIS | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BG (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005441-38 | Sponsor Protocol Number: F1K-MC-EVDP | Start Date*: 2008-03-07 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Efficacy and Safety of Drotrecogin Alfa (Activated) in Adult Patients with Septic Shock | |||||||||||||
| Medical condition: Septic shock | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) NL (Completed) FR (Completed) BE (Completed) IT (Completed) PT (Completed) FI (Completed) CZ (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006315-68 | Sponsor Protocol Number: B3D-EW-GHDH | Start Date*: 2007-05-07 |
| Sponsor Name:Eli Lilly and Company Limited | ||
| Full Title: Comparison of the Effects of Teriparatide with those of Risendronate on Lumbar Spine Volumetric Bone Mineral Density in GLucocorticpid-Induced Osteoporosis in Men | ||
| Medical condition: Males with glucocorticoid-induced osteoporosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Completed) GR (Completed) ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004418-40 | Sponsor Protocol Number: H9H-MC-JBAL | Start Date*: 2012-02-23 | |||||||||||
| Sponsor Name:Lilly S.A, | |||||||||||||
| Full Title: A Phase 2 Study of LY2157299 Monohydrate Monotherapy or LY2157299 Monohydrate plus Lomustine Therapy compared to Lomustine Monotherapy in Patients with Recurrent Glioblastoma | |||||||||||||
| Medical condition: Glioblastoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002649-69 | Sponsor Protocol Number: I1F-EW-RHBZ | Start Date*: 2015-12-09 | |||||||||||
| Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
| Full Title: A 24-Week Multicenter, Randomized, Open-Label, Parallel Group Study Comparing the Efficacy and Safety of Ixekizumab to Fumaric Acid Esters and Methotrexate in Patients with Moderate-to-Severe Plaqu... | |||||||||||||
| Medical condition: Moderate-to-Severe Plaque Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002374-39 | Sponsor Protocol Number: I8B-MC-ITSI | Start Date*: 2017-12-27 | |||||||||||
| Sponsor Name:Lilly S.A. | |||||||||||||
| Full Title: Protocol I8B-MC-ITSI A Prospective, Randomized, Double-Blind, Crossover Comparison Evaluating Compatibility and Safety of LY900014 and Insulin Lispro with an External Continuous Subcutaneous Insuli... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000748-14 | Sponsor Protocol Number: H6Q-MC-S042 | Start Date*: 2008-05-30 |
| Sponsor Name:Eli Lilly and Company limited | ||
| Full Title: An Open Label, Multicenter Phase 2 Study of Single-Agent Enzastaurin HCl in Previously Treated Waldenstrom’s Macroglobulinemia or Multiple Myeloma | ||
| Medical condition: Waldenstrom’s Macroglobulinemia or Multiple Myeloma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002112-99 | Sponsor Protocol Number: F1K-MC-EVDK | Start Date*: 2006-09-26 | |||||||||||
| Sponsor Name:Eli Lilly & Company Limited | |||||||||||||
| Full Title: A Phase 2 Study to Evaluate Dose and Duration of Treatment of Drotrecogin Alfa (Activated) Using Serial Measurements of Protein C in Patients with Severe Sepsis and Multiple Organ Dysfunction | |||||||||||||
| Medical condition: severe sepsis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) SE (Prematurely Ended) FR (Completed) FI (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011739-11 | Sponsor Protocol Number: H3E-EW-S128 | Start Date*: 2009-08-04 | ||||||||||||||||
| Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
| Full Title: Phase 2 Study of Pemetrexed and Cisplatin as Induction, Followed by Pemetrexed and Cisplatin with Concurrent Thoracic Radiotherapy, in Patients with Unresectable Locally-Advanced Stage III, Non-Squ... | ||||||||||||||||||
| Medical condition: Non-small Cell Lung Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) ES (Completed) IT (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000622-55 | Sponsor Protocol Number: I5S-MC-EFJE | Start Date*: 2013-07-31 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2 Efficacy and Safety Dose-Ranging Study of LY3015014 in Patients with Primary Hypercholesterolemia | |||||||||||||
| Medical condition: Primary hypercholesterolaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) NL (Completed) PL (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000900-15 | Sponsor Protocol Number: B7A-MC-MBCU | Start Date*: 2005-08-19 |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: The effect of Ruboxistaurin on Clinically Significant Macular Edema in Patients with Diabetes Mellitus, as assessed by Optical Coherence Tomography | ||
| Medical condition: Diabetic Macular Edema (DME), is the most common cause of visual impairment in patients with diabetic retinopathy (DR). It is the accumulation of extracellular fluid in the retinal tissues of the m... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DK (Completed) DE (Completed) ES (Completed) LT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004866-16 | Sponsor Protocol Number: I5E-MC-TSAT | Start Date*: 2013-06-06 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Parallel Study with an Open-Label Extension to Assess the Impact of Testosterone Solution on Total Testosterone, Sex Drive and Energy in Hypogonadal Men. | |||||||||||||
| Medical condition: Male hypogonadism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004630-41 | Sponsor Protocol Number: H6Q-MC-JCBJ | Start Date*: 2006-04-26 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 3 Clinical Study to Investigate the Prevention of Relapse in Lymphoma Using Daily Enzastaurin | |||||||||||||
| Medical condition: high-risk diffuse large B-cell lymphoma (DLBCL ) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) HU (Completed) ES (Prematurely Ended) DK (Prematurely Ended) BE (Prematurely Ended) PT (Prematurely Ended) DE (Prematurely Ended) GR (Prematurely Ended) IT (Completed) GB (Prematurely Ended) CZ (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000167-95 | Sponsor Protocol Number: Protocol F1J-MC-HMDI | Start Date*: 2005-03-03 |
| Sponsor Name:Eli Lilly and Company Limited | ||
| Full Title: Duloxetine Versus Placebo in the Prevention of Recurrence of Major Depressive Disorder | ||
| Medical condition: Major Depressive Disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) IT (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-005156-94 | Sponsor Protocol Number: I3Y-MC-JPCE | Start Date*: 2016-06-15 | ||||||||||||||||
| Sponsor Name:Eli Lilly and Company | ||||||||||||||||||
| Full Title: Protocol I3Y-MC-JPCE A Phase 1b Study of Abemaciclib in Combination with Pembrolizumab for Patients with Stage IV Non-Small Cell Lung Cancer or Hormone Receptor Positive, HER2 Negative Breast Cancer | ||||||||||||||||||
| Medical condition: Stage IV Non-Small Cell Lung Cancer or Hormone Receptor Positive, HER2 Negative Breast Cancer | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Trial now transitioned) ES (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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