- Trials with a EudraCT protocol (980)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
980 result(s) found for: Chronic liver disease.
Displaying page 1 of 49.
EudraCT Number: 2018-001334-18 | Sponsor Protocol Number: CarPAs | Start Date*: 2020-09-10 | ||||||||||||||||
Sponsor Name:Associazione Italiana Pazienti Leucemia Mieloide Cronica (AIPLMC) | ||||||||||||||||||
Full Title: Cardiovascular assessment of Ponatinib as treatment option in chronic phase chronic myeloid leukemia after failure of Imatinib and Bosutinib (CarPAs) | ||||||||||||||||||
Medical condition: Chronic Myeloid Leukemia (CML) in Chronic Phase (CP) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003780-50 | Sponsor Protocol Number: B1871008 | Start Date*: 2008-07-30 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc, a wholly owned subsidiary of Pfizer Inc, 500 Arcola Road, Collegeville, PA 19426 USA | |||||||||||||
Full Title: A Phase 3 Randomized, Open-Label Study of Bosutinib Versus Imatinib in Subjects With Newly Diagnosed Chronic Phase Philadelphia Chromosome Positive Chronic Myelogenous Leukemia | |||||||||||||
Medical condition: Chronic myelogenous leukemia (CML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (Completed) BE (Completed) ES (Completed) LV (Completed) LT (Completed) FR (Completed) IT (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002987-24 | Sponsor Protocol Number: 152CL201 | Start Date*: 2007-06-25 | |||||||||||
Sponsor Name:Biogen Idec Ltd | |||||||||||||
Full Title: A Randomized, Open-Label, Multicenter, Phase 2 Study to Evaluate the Safety and Efficacy of Lumiliximab in Combination with Fludarabine, Cyclophosphamide, and Rituximab Versus Fludarabine, Cyclopho... | |||||||||||||
Medical condition: Relapsed Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Prematurely Ended) ES (Completed) IT (Prematurely Ended) FR (Completed) DE (Prematurely Ended) GB (Completed) CZ (Prematurely Ended) SK (Completed) PT (Prematurely Ended) LT (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003114-12 | Sponsor Protocol Number: HBIG | Start Date*: 2022-11-04 | ||||||||||||||||
Sponsor Name:Medical University of Graz | ||||||||||||||||||
Full Title: Impact of Hepatitis B immunoglobulins in patients with chronic Hepatitis B on Hepatocellular Carcinoma – a proof of concept study | ||||||||||||||||||
Medical condition: Patients with both chronic hepatitis B and hepatocellular carcinoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-006023-33 | Sponsor Protocol Number: SIMFIB | Start Date*: 2021-10-26 | ||||||||||||||||
Sponsor Name:Institut d’Investigacions Biomèdiques August Pi i Sunyer | ||||||||||||||||||
Full Title: Efficacy of simvastatin reducing liver fibrosis in patients with advanced fibrosis due to alcohol: a randomized, double-blind, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: reduction of liver fibrosis in patients with advanced fibrosis due to alcohol | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001222-83 | Sponsor Protocol Number: HHSC/001 | Start Date*: 2005-12-09 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A phase I/II safety and tolerability dose escalation study following the autologous infusion of expanded adult haemopoietic stem cells to patients with liver insufficiency | ||||||||||||||||||
Medical condition: Chronic liver insufficiency | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2015-000963-15 | Sponsor Protocol Number: MATCH0.1 | Start Date*: 2016-01-19 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: MAcrophage Therapy for Liver Cirrhosis (MATCH) | |||||||||||||
Medical condition: Liver Cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006694-24 | Sponsor Protocol Number: IV-A05-LL-01-PR.03 | Start Date*: 2007-07-16 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Phase I/II dose-escalation study of the investigational trifunctional bispecific anti-CD20 x anti-CD3 antibody FBTA05 in relapsed or refractory chronic lymphocytic leukemia | |||||||||||||
Medical condition: relapsed or refractory Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003012-35 | Sponsor Protocol Number: HM07/8281 | Start Date*: 2012-06-12 | |||||||||||
Sponsor Name:Leeds Teaching Hospitals NHS Trust | |||||||||||||
Full Title: CLARET: CLL Levels following Alemtuzumab in Responders to Early Therapy: A randomised, phase III trial to assess alemtuzumab consolidation therapy in patients with chronic lymphocytic leukaemia (CL... | |||||||||||||
Medical condition: Chronic lymphocytic leukaemia (CLL). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001824-30 | Sponsor Protocol Number: BEN-CAM | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:Associazione Malattie Sangue Onlus | |||||||||||||
Full Title: Phase II study of the combination Bendamustine and sc Alemtuzumab for patients with refractory or relapsed B-cell chronic lynphocytic leukemia | |||||||||||||
Medical condition: patients whit LLC | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001454-24 | Sponsor Protocol Number: IPSS B025-L | Start Date*: 2005-06-08 | |||||||||||
Sponsor Name:RIEMSER Arzneimittel AG | |||||||||||||
Full Title: An Open Labelled, Clinical Phase II Study With Oral Cis-U-Hydroxy-L-Proline (CHP) in 45 Patients With: - Chronic viral hepatitis - Chronic alcoholic liver diseases without cirrhosis - Compens... | |||||||||||||
Medical condition: Chronic viral hepatitis, Chronic alcoholic liver diseases without cirrhosis, Compensated alcoholic liver cirrhosis, Primary Billiary Cirrhosis or Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004672-11 | Sponsor Protocol Number: SNOXA12C201 | Start Date*: 2012-03-05 | |||||||||||
Sponsor Name:NOXXON Pharma AG | |||||||||||||
Full Title: A multi-centre, open label, uncontrolled, Phase IIa clinical trial evaluating the safety and efficiacy of NOX-A12 in combination with a background therapy of bendamustine and rituximab (BR) in prev... | |||||||||||||
Medical condition: Relapsed chronic lymphocytic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) IT (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001677-15 | Sponsor Protocol Number: 08/H0808/2 | Start Date*: 2008-07-21 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: The effect of intraoperative N-acetylcysteine on hepatocellular injury during laparoscopic bariatric surgery. A randomised controlled trial. | |||||||||||||
Medical condition: Non-Alcoholic Fatty Liver Disease in patients undergoing weight-loss (bariatric) surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019695-76 | Sponsor Protocol Number: MKI113006 | Start Date*: 2010-11-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-centre, Dose Ranging Study to Evaluate the Efficacy and Safety of Losmapimod (GW856553) Tablets Administered Twice Daily compar... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010808-28 | Sponsor Protocol Number: HBV BID | Start Date*: 2010-02-10 | ||||||||||||||||
Sponsor Name:Kings College Hospital NHS Foundation Trust [...] | ||||||||||||||||||
Full Title: Role of Non-invasive test in detecting fibrosis in chronic hepatitis B patients | ||||||||||||||||||
Medical condition: Level of fibrosis in patients with chronic Hepatitis B(HBV). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001805-18 | Sponsor Protocol Number: Emera003 | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:NBMI Science AB | |||||||||||||
Full Title: A randomised, placebo-controlled, blinded, cross-over, pilot study to explore safety and efficacy of NBMI treatment of patients with mild, moderate and severe Chronic Obstructive Pulmonary Disease ... | |||||||||||||
Medical condition: Patients with Chronic Obstructive Pulmonary Disease (COPD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003547-36 | Sponsor Protocol Number: NRL972-09/2008- (CHBC) | Start Date*: 2009-02-12 | |||||||||||
Sponsor Name:Norgine Ltd | |||||||||||||
Full Title: An open study to investigate the effects of chronic hepatitis B or C on the pharmacokinetics of cholyl-lysyl-fluorescein (NRL972) before, during and after standard treatment | |||||||||||||
Medical condition: In-vivo diagnostic marker for liver dysfunction. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004339-19 | Sponsor Protocol Number: UTX-TGR-204 | Start Date*: 2017-02-16 | |||||||||||
Sponsor Name:TG Therapeutics | |||||||||||||
Full Title: A Multi-Center, Open-Label, Compassionate Use Extension Study of Ublituximab (TG-1101) in Combination with Umbralisib (TGR-1202) for Patients Previously Enrolled in Protocol UTX-TGR-304 | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002992-27 | Sponsor Protocol Number: 201496 | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: 201496: A Study to Evaluate the Efficacy and Safety of 15mg BID Losmapimod (GW856553) Compared to Placebo in Frequently Exacerbating Subjects with Chronic Obstructive Pulmonary Disease (COPD). | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) DE (Completed) BG (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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