- Trials with a EudraCT protocol (4,648)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (12)
4,648 result(s) found for: Liver Disease.
Displaying page 7 of 233.
EudraCT Number: 2012-000454-58 | Sponsor Protocol Number: S53657 | Start Date*: 2012-04-18 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Prospective, monocentre phase I study of sequential infusion of Y90-labeled microspheres and Mitomycine C in patients with chemorefractory liver metastases from breast carcinoma | ||
Medical condition: chemorefractory liver metastases from breast carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001177-32 | Sponsor Protocol Number: HEP101 | Start Date*: 2016-08-09 | ||||||||||||||||
Sponsor Name:Promethera Biosciences | ||||||||||||||||||
Full Title: Multicenter Phase II Safety and Preliminary Efficacy Study of 2 dose regimens of HepaStem in Patients with Acute on Chronic Liver Failure | ||||||||||||||||||
Medical condition: The study will recruit cirrhotic patients who are hospitalized for Acute-on-chronic liver failure (ACLF) or Acute Decompensation at risk of developing ACLF. ACLF combines an acute deterioration of... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001552-29 | Sponsor Protocol Number: 1271/2014 | Start Date*: 2014-06-20 |
Sponsor Name:Medizinische Universität Wien, Abteilung für Anästhesie und allgemeine Intensivmedizin | ||
Full Title: Determination of the minimal alveolar concentration of Sevoflurane in patient with end stage liver disease | ||
Medical condition: Orthotopic liver transplantation (OLT) is the only therapy for patients with liver failure. These patients have reduced anesthetic requirements compared with healthy patients. Sevoflurane has prove... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004594-44 | Sponsor Protocol Number: NN9931-4553 | Start Date*: 2021-06-28 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: The effect of semaglutide in subjects with non-cirrhotic non-alcoholic steatohepatitis | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) DE (Ongoing) IE (Trial now transitioned) CZ (Trial now transitioned) GR (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) SK (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) BG (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) HR (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001002-26 | Sponsor Protocol Number: MPSA-153-001 | Start Date*: 2020-08-12 | |||||||||||
Sponsor Name:NERVIANO MEDICAL SCIENCES SRL | |||||||||||||
Full Title: Phase I/II study on safety and efficacy of NMS-01940153E in adult patients with unresectable hepatocellular carcinoma (HCC) previously treated with systemic therapy. | |||||||||||||
Medical condition: Unresectable hepatocellular carcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003606-53 | Sponsor Protocol Number: CA224106 | Start Date*: 2022-06-14 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2, Safety Confirmation and Double-blind, Placebo-controlled, Randomized Study of Relatlimab in Combination with Nivolumab and Bevacizumab in Treatment-naive Advanced/Metastatic Hepatocell... | |||||||||||||
Medical condition: Advanced/metastatic hepatocellular carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) ES (Temporarily Halted) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006637-14 | Sponsor Protocol Number: A6181170 | Start Date*: 2008-09-01 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, 10017 | |||||||||||||
Full Title: A MULTINATIONAL, RANDOMIZED, OPEN-LABEL, PHASE 3 STUDY OF SUNITINIB MALATE VERSUS SORAFENIB IN PATIENTS WITH ADVANCED HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) FR (Completed) DE (Prematurely Ended) BE (Completed) IT (Prematurely Ended) SE (Prematurely Ended) HU (Completed) CZ (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000673-30 | Sponsor Protocol Number: HAN-HCC-001 | Start Date*: 2007-06-01 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: Placebo kontrollierte Phase II Studie zur Therapie des fortgeschrittenen HCC mit Viscum fraxini | |||||||||||||
Medical condition: Advanced hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002166-20 | Sponsor Protocol Number: AMELIORATE | Start Date*: 2012-02-08 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Treatment of hepatorenal syndrome with terlipressin infusion adjusted to hemodynamic response | ||||||||||||||||||
Medical condition: Hepatorenal syndrome (HRS) type 1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000752-41 | Sponsor Protocol Number: E7050-701 | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:Eisai Inc. | |||||||||||||
Full Title: An Open-Label, Multicenter, Randomized, Phase Ib/II Study of E7050 in Combination with Sorafenib versus Sorafenib Alone as First Line Therapy in Patients with Hepatocellular Carcinoma | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024651-86 | Sponsor Protocol Number: TEHYLIC | Start Date*: 2011-05-30 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Randomized Trial, Masked, and Placebo Controlled to Assess the Effects of Sapropterin on Hepatic and Systemic Hemodynamics in Patients With Liver Cirrhosis and Portal Hypertension | ||||||||||||||||||
Medical condition: Cirrosis hepática, Hipertensión portal | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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: 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: 2009-018034-11 | Sponsor Protocol Number: 2010vanco.psc | Start Date*: 2013-04-29 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Open pilot study of treatment with vancomycin to children and adolescents with primary sclerosing cholangitis | ||
Medical condition: Primary Sclerosing Cholangitis (PSC) is a progressive disease of the biliary system which might lead to increased risk of cholangiocancer. PSC constitutes a common indication for adult liver transp... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000525-30 | Sponsor Protocol Number: A6181055 | Start Date*: 2006-06-14 | |||||||||||
Sponsor Name:Pfizer Hellas A.E. | |||||||||||||
Full Title: AN OPEN LABEL INTERNATIONAL MULTI-CENTER PHASE 2 ACTIVITY AND SAFETY STUDY OF SU011248 IN PATIENTS WITH UNRESECTABLE HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: Histologically confirmed diagnosis of hepatocellular carcinoma. Patients with the fibrolamellar histology or a mixed histology are not eligible. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000144-18 | Sponsor Protocol Number: CDKO-125a-010 | Start Date*: 2017-08-01 | |||||||||||
Sponsor Name:Tiziana Life Sciences Plc | |||||||||||||
Full Title: Phase IIA Exploratory Study of Oral Milciclib Maleate in Patients with Unresectable or Metastatic Hepatocellular Carcinoma | |||||||||||||
Medical condition: Uunresectable or metastatic hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000369-54 | Sponsor Protocol Number: 60725 | Start Date*: 2018-06-27 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Intra-arterial Lutetium-177- dotatate for treatment of patients with neuroendocrine tumor liver metastases | ||
Medical condition: Patients with neuro-endocrine tumors with liver metastases with an indication for treatment with lutetium-177-dotatate | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003629-13 | Sponsor Protocol Number: PROFIT | Start Date*: 2018-01-31 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: A Prospective, randomised placebo controlled feasibility trial of Faecal Microbiotica Transplantation in cirrhosis | |||||||||||||
Medical condition: Cirrhosis of the liver | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001103-32 | Sponsor Protocol Number: HEPCOViVac | Start Date*: 2021-04-26 |
Sponsor Name:Medical University of Graz | ||
Full Title: The HEPCOViVac Registry - Immunological response in patients with liver disease vaccinated against COVID-19 | ||
Medical condition: Cirrhotic chronic liver disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005679-33 | Sponsor Protocol Number: KKSH-042 | Start Date*: 2011-01-20 | ||||||||||||||||
Sponsor Name:Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg | ||||||||||||||||||
Full Title: Influence of the selective endothelin receptor-blocker Ambrisetan on the portal pressure in patients with cirrhosis | ||||||||||||||||||
Medical condition: Portal hypertension and hepatic cirrhosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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