- 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 3 of 54.
| EudraCT Number: 2016-004675-52 | Sponsor Protocol Number: I4V-MC-JAHA | Start Date*: 2017-07-11 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, 24 Week Study Followed by Long-Term Treatment for Evaluation of Efficacy and Safety of Baricitinib in Patients with Active Psoriatic Art... | |||||||||||||
| Medical condition: Active Psoriatic Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) ES (Prematurely Ended) HU (Completed) PL (Prematurely Ended) IT (Completed) RO (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003490-33 | Sponsor Protocol Number: H9X-MC-GBGL | Start Date*: 2018-04-23 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Parallel Arm Study of the Efficacy and Safety of Investigational Dulaglutide Doses When Added to Metformin in Patients with Type 2 Diabetes Mellitus | |||||||||||||
| Medical condition: Type 2 Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) GR (Completed) AT (Completed) HU (Completed) PL (Completed) ES (Completed) IT (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004614-18 | Sponsor Protocol Number: I6T-MC-AMAM | Start Date*: 2019-07-10 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Treat-Through Study to Evaluate the Efficacy and Safety of Mirikizumab in Patients with Moderately to Severely Acti... | |||||||||||||
| Medical condition: moderately to severely active Crohn’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) HU (Completed) FR (Completed) GB (GB - no longer in EU/EEA) DE (Completed) NL (Completed) ES (Completed) PL (Completed) DK (Completed) BE (Completed) SK (Completed) LT (Completed) CZ (Completed) LV (Completed) HR (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018759-82 | Sponsor Protocol Number: F3Z-EW-IOPT | Start Date*: 2010-06-16 |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: The Effect of Postprandial Hyperglycemia on Arterial Stiffness in Patients with Type 2 Diabetes | ||
| Medical condition: Type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003331-38 | Sponsor Protocol Number: I1F-MC-RHCD | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Multicenter, Double-Blind, Randomized, Active- and Placebo Controlled Study to Evaluate Safety, Tolerability, and Efficacy of Ixekizumab in Patients from 6 to Less than 18 Years of Age with Moderat... | |||||||||||||
| Medical condition: Moderate-to-Severe Plaque Psoriasis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) ES (Completed) PL (Completed) HU (Completed) CZ (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003791-23 | Sponsor Protocol Number: I4T-MC-JVDB | Start Date*: 2015-04-23 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Protocol I4T-MC-JVDB Randomized Phase 2 Trial Evaluating Pharmacokinetics and Safety of Four Ramucirumab Dosing Regimens in Second Line Gastric or Gastroesophageal Junction Adenocarcinoma | |||||||||||||
| Medical condition: Second Line Gastric or Gastroesophageal Junction Adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) SK (Completed) FR (Completed) PL (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002537-39 | Sponsor Protocol Number: H3E-IT-S079 | Start Date*: 2005-04-04 | |||||||||||
| Sponsor Name:ELI LILLY | |||||||||||||
| Full Title: Phase II Trial of Neoadjuvant ALIMTA plus Cisplatin followed by Surgery and Radiation in the Treatment of Pleural Mesothelioma | |||||||||||||
| Medical condition: Plaural Mesothelioma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000225-51 | Sponsor Protocol Number: ITP-NODAT | Start Date*: 2012-11-21 |
| Sponsor Name:Fundació Institut Mar d'investigacions Mediques | ||
| Full Title: Insulin Therapy for the Prevention of New Onset Diabetes after Transplantation (ITP-NODAT) Prospective Study in Non-Diabetic De Novo Kidney Transplant Recipients | ||
| Medical condition: Previously non-diabetic end stage renal disease patients undergoing kidney transplantation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012713-22 | Sponsor Protocol Number: version 28.10.2009 | Start Date*: 2010-05-06 |
| Sponsor Name:Medizinische Universität Wien, Univ. Klinik für Anästhesie, Allg. Intensivmedizin u Schmerztherapie | ||
| Full Title: Randomized Double-blind Study Comparing the Efficacy of Duloxetine with Placebo in Patients with Chronic Low Back Pain | ||
| Medical condition: efficacy of duloxetine in the treatment of patients with chronic low back pain to placebo | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003424-31 | Sponsor Protocol Number: I4V-MC-JAGA | Start Date*: Information not available in EudraCT |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: Treatment of Conditions Expected to Benefit from JAK 1/2 Inhibition: CANDLE, CANDLE-Related Conditions, SAVI, and Severe Juvenile Dermatomyositis | ||
| Medical condition: CANDLE, CANDLE-Related Conditions, SAVI, and Severe Juvenile Dermatomyositis, Aicardi-Goutieres Syndrome | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002495-13 | Sponsor Protocol Number: J1B-MC-FRCF | Start Date*: 2020-04-20 | |||||||||||
| Sponsor Name:Eli Lilly & Company | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Crossover Study to Evaluate the Efficacy and Safety of LY3454738 in Adults with Chronic Spontaneous Urticaria Inadequately Contr... | |||||||||||||
| Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001194-25 | Sponsor Protocol Number: H6D-MC-LVJJ | Start Date*: 2013-09-25 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Tadalafil for Duchenne Muscular Dystrophy | |||||||||||||
| Medical condition: Duchenne Muscular Dystrophy | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: GB (Prematurely Ended) IT (Prematurely Ended) DE (Completed) ES (Prematurely Ended) BE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004585-25 | Sponsor Protocol Number: I1F-MC-RHCF | Start Date*: 2017-05-26 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A 52-Week Multicenter, Randomized, Open-Label, Parallel-Group Study Evaluating the Efficacy and Safety of Ixekizumab versus Adalimumab in Patients with Psoriatic Arthritis Who Are Biologic Disease-... | |||||||||||||
| Medical condition: Psoriatic Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) FI (Completed) DE (Completed) NL (Completed) BE (Completed) AT (Completed) SE (Completed) DK (Completed) ES (Completed) GB (Completed) FR (Completed) IT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004092-31 | Sponsor Protocol Number: I6T-MC-AMAP | Start Date*: 2018-06-25 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: I6T-MC-AMAP A Phase 3, Multicenter, Open-Label Extension Study to Evaluate the Long- Term Efficacy and Safety of Mirikizumab in Patients with Moderately to Severely Active Ulcerative Colitis (LU... | |||||||||||||
| Medical condition: moderately to severely active Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) LT (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) DK (Trial now transitioned) LV (Trial now transitioned) PL (Trial now transitioned) FR (Trial now transitioned) DE (Completed) ES (Ongoing) AT (Trial now transitioned) SK (Trial now transitioned) HR (Prematurely Ended) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003339-53 | Sponsor Protocol Number: I8H-MC-BDCL | Start Date*: 2020-09-22 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2, Parallel, Comparator-Controlled Trial to Evaluate the Safety and Efficacy of LY3209590 in Insulin-Naïve Patients with Type 2 Diabetes Mellitus | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004243-23 | Sponsor Protocol Number: J1S-MS-JV02 | Start Date*: 2021-05-10 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Open-Label Phase 2 Study Evaluating Ramucirumab in Pediatric Patients and Young Adults with relapsed, Recurrent, or Refractory Synovial Sarcoma. | |||||||||||||
| Medical condition: Synovial Sarcoma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) BE (Completed) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004242-42 | Sponsor Protocol Number: J1S-MC-JV01 | Start Date*: 2021-05-12 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Open-Label Phase 2 Study Evaluating Ramucirumab in Pediatric Patients and Young Adults with Relapsed, Recurrent, or Refractory Desmoplastic Small Round Cell Tumor. | |||||||||||||
| Medical condition: Desmoplastic small round cell tumour (DSRCT) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000079-35 | Sponsor Protocol Number: J2J-OX-JZLC | Start Date*: 2021-11-02 |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: EMBER-3: A Phase 3, Randomized, Open-Label Study of Imlunestrant, Investigator’s Choice of Endocrine Therapy, and Imlunestrant plus Abemaciclib in Patients with Estrogen Receptor Positive, HER2 Neg... | ||
| Medical condition: Breast Neoplasms, Neoplasm Metastasis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) DE (Ongoing) CZ (Completed) FR (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) GR (Trial now transitioned) NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004737-33 | Sponsor Protocol Number: 5706 | Start Date*: 2018-05-16 | ||||||||||||||||
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||||||||||||||||||
| Full Title: A prospective, multicenter, randomized, open-label study of 12 week duration to evaluate the effect of VILDagliptin added to insulin on glycaemic control in haemoDIALyzed patients with type 2 diabe... | ||||||||||||||||||
| Medical condition: haemodialyzed patients with type 2 diabetes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003365-34 | Sponsor Protocol Number: I4V-MC-JAIV | Start Date*: 2019-05-02 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Proof-of-Concept Study Evaluating the Efficacy and Safety of Baricitinib (LY3009104) in Patients with Primary Biliary Cholangitis Who Have an Inadeq... | |||||||||||||
| Medical condition: Primary Biliary Cholangitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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