- Trials with a EudraCT protocol (88)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
88 result(s) found for: Nonalcoholic fatty liver.
Displaying page 1 of 5.
EudraCT Number: 2008-008275-34 | Sponsor Protocol Number: Edi-Omeg3-08001 | Start Date*: 2009-08-20 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: The Effect of Omega-3 Fatty Acids on Non-Alcoholic Fatty Liver Disease | |||||||||||||
Medical condition: Non-alcoholic fatty liver disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006677-26 | Sponsor Protocol Number: 68797373 | Start Date*: 2022-06-22 | ||||||||||||||||
Sponsor Name:Maastricht University | ||||||||||||||||||
Full Title: Metabolic effects of ketohexokinase inhibition in individuals with non-alcoholic fatty liver disease | ||||||||||||||||||
Medical condition: Healthy volunteers (non-alcoholic fatty liver disease) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003164-21 | Sponsor Protocol Number: 652-2-203 | Start Date*: 2015-01-05 | |||||||||||
Sponsor Name:Tobira Therapeutics, Inc., a subsidiary of Allergan plc | |||||||||||||
Full Title: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects with Liver Fibrosis | |||||||||||||
Medical condition: Nonalcoholic Steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) IT (Completed) DE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005187-63 | Sponsor Protocol Number: FM101-CTP2-001 | Start Date*: 2021-04-14 | ||||||||||||||||
Sponsor Name:Future Medicine Co., Ltd. | ||||||||||||||||||
Full Title: A Randomized Phase 2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of FM101 in Adults with Nonalcoholic Fatty Liver Disease (NAFLD) or Nonalcoholic Steatohepatitis (NASH) | ||||||||||||||||||
Medical condition: Nonalcoholic Fatty Liver Disease (NAFLD) or Nonalcoholic Steatohepatitis (NASH) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021515-17 | Sponsor Protocol Number: N/A | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: RiFL: Rifaxamin in Fatty Liver Disease. Does Modulation of Gut Microbiota Reduce Hepatic Inflammation in Non-Alcoholic Steatohepatitis (NASH)? | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005531-28 | Sponsor Protocol Number: Urso in Obese | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name:Hanns-Ulrich Marschall | |||||||||||||
Full Title: Ursodeoxycholic Acid in Morbidly Obese Patients Before Bariatric Surgery | |||||||||||||
Medical condition: Patients with morbid obesity (MB) are investigated. MB is very frequently (90%) associated with non-alcoholic fatty liver disease (NAFLD) comprising a spectrum reaching from steatosis (NAFL) over s... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003766-26 | Sponsor Protocol Number: 25-12-59 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Southampton University Hospitals NHS Trust | |||||||||||||
Full Title: The effects of purified n-3 fatty acids on serum biomarkers and cardiovascular risk markers in a randomized placebo controlled trial in patients with non alcoholic fatty liver disease | |||||||||||||
Medical condition: Non alcoholic fatty liver disease (NAFLD). This fatty liver disease may progress to a chronic condition that sometimes deteriorates further to cirrhosis and even liver carcinoma. To date there is n... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003168-37 | Sponsor Protocol Number: CAIN457ADE15 | Start Date*: 2019-12-04 | ||||||||||||||||
Sponsor Name:Novartis Pharma GmbH | ||||||||||||||||||
Full Title: A randomized, double-blind, multicenter, 24-week study of subcutaneous secukinumab to assess anti-interleukin-17A treatment in plaque psoriasis patients with coexisting non-alcoholic fatty liver di... | ||||||||||||||||||
Medical condition: plaque psoriasis with coexisting non-alcoholic fatty liver disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003013-14 | Sponsor Protocol Number: EFC10144 | Start Date*: 2008-02-01 | |||||||||||
Sponsor Name:sanofi-aventis recherche & development | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, parallel group study of rimonabant 20 mg daily for the treatment of Type 2 diabetic patients with nonalcoholic steatohepatitis (NASH) | |||||||||||||
Medical condition: Diabetic patients with Non-Alcoholic Steato-Hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) BE (Completed) DE (Prematurely Ended) HU (Prematurely Ended) ES (Completed) IT (Prematurely Ended) FR (Suspended by CA) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003012-61 | Sponsor Protocol Number: EFC10143 | Start Date*: 2008-02-01 | |||||||||||
Sponsor Name:sanofi recherche & developpement | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, parallel group study of rimonabant 20 mg daily for the treatment of non-diabetic patients with nonalcoholic steatohepatitis (NASH) | |||||||||||||
Medical condition: Non diabetic patients with Non-Alcoholic Steato-Hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) DE (Prematurely Ended) BE (Completed) ES (Completed) HU (Prematurely Ended) IT (Prematurely Ended) FR (Suspended by CA) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000813-37 | Sponsor Protocol Number: OCABSGS | Start Date*: 2012-05-16 | |||||||||||
Sponsor Name:Sahlgrenska Academy | |||||||||||||
Full Title: Effects of obeticholic acid on hepatic fatty acid/triglyceride metabolism and hepatobiliary detoxification/elimination in morbidly obese and gallstone patients. | |||||||||||||
Medical condition: Fatty liver disease, morbid obesity, gallstone disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001975-36 | Sponsor Protocol Number: 201200197536 | Start Date*: 2012-05-24 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Evaluation on the efficacy of docosahexaenoic acid for the treatment of nonalcoholic fatty liver disease in children | |||||||||||||
Medical condition: Nonalcoholic steatohepatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004605-38 | Sponsor Protocol Number: NUC-4/NAS | Start Date*: 2015-02-11 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase II dose-finding study comparing different doses of norursodeoxycholic acid capsules with placebo in the treatment of non-alcoholic fatty liver di... | |||||||||||||
Medical condition: Non-alcoholic fatty liver disease (NAFLD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015166-62 | Sponsor Protocol Number: EME-08/43/15 | Start Date*: 2010-11-16 | |||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial of Losartan as an anti-fibrotic agent in non-alcoholic steatohepatitis. | |||||||||||||
Medical condition: Fibrosis in patients with non-alcoholic steatohepatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000645-12 | Sponsor Protocol Number: GFT505-219-8 | Start Date*: 2019-09-03 | |||||||||||
Sponsor Name:GENFIT SA | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Cross-over Phase II Study to Evaluate the Effect of a 6-week Elafibranor (120mg) treatment administered once daily on hepatic lipid composition in subjects with ... | |||||||||||||
Medical condition: Subjects with Nonalcoholic Fatty Liver (NAFL) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001046-19 | Sponsor Protocol Number: ORA-D-N01B | Start Date*: 2020-08-13 |
Sponsor Name:Oramed Ltd. | ||
Full Title: An Open-Label Multi-Center Study to Assess the Safety and Potential of Oral Insulin to Reduce Liver Fat Content in Type 2 Diabetes Patients with Nonalcoholic Steatohepatitis (NASH) | ||
Medical condition: Type 2 Diabetes Patients with Nonalcoholic Steatohepatitis (NASH) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021368-13 | Sponsor Protocol Number: MTQ-LD-001 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:Antipodean Pharmaceuticals | |||||||||||||
Full Title: A Double-blind Randomised Placebo-controlled Multicentre Study of 40mg MitoQ and Placebo for the Treatment of Participants with Raised Liver Enzymes due to Non-Alcoholic Fatty Liver Disease (NAFLD) | |||||||||||||
Medical condition: Raised Liver Enzymes due to Non-Alcoholic Fatty Liver Disease (NAFLD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002560-16 | Sponsor Protocol Number: 747-303 | Start Date*: 2015-12-10 | |||||||||||
Sponsor Name:Intercept Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, Long-Term, Placebo-Controlled, Multicenter Study Evaluating the Safety and Efficacy of Obeticholic Acid in Subjects with Nonalcoholic Steatohepatitis | |||||||||||||
Medical condition: Nonalcoholic steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) AT (Completed) SE (Completed) BE (Completed) DK (Completed) ES (Completed) FI (Completed) PT (Prematurely Ended) HU (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002253-29 | Sponsor Protocol Number: CEC-11/NAS | Start Date*: 2022-03-08 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase II dose-finding study comparing different doses of ZED1227 capsules with placebo in the treatment of non-alcoholic fatty liver disease (NAFLD) wi... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002325-37 | Sponsor Protocol Number: H80-MC-O008 | Start Date*: 2008-07-08 | |||||||||||
Sponsor Name:Department of Medicine I, University Hospital St. Josef-Hospital, Ruhr University Bochum | |||||||||||||
Full Title: Effects of Exenatide (Byetta®) on biochemical and histological parameters of liver function in patients with Nonalcoholic Steatohepatitis (NASH) – a randomized, placebo-controlled, parallel-group t... | |||||||||||||
Medical condition: Non alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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