- Trials with a EudraCT protocol (4,649)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4,649 result(s) found for: Liver Disease.
Displaying page 10 of 233.
| EudraCT Number: 2009-010806-12 | Sponsor Protocol Number: COLO400A2430 | Start Date*: 2009-07-22 | ||||||||||||||||
| Sponsor Name:Novartis Farmacéutica S.A | ||||||||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, abierto, controlado para comparar la Respuesta Virológica Sostenida durante el tratamiento con Sandimmun Neoral® o tacrolimus en el mantenimiento de receptores ... | ||||||||||||||||||
| Medical condition: pacientes con trasplante hepático con infección recurrente por Hepatitis C | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) BE (Completed) IT (Completed) HU (Completed) FR (Completed) DE (Completed) AT (Completed) GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-010396-25 | Sponsor Protocol Number: PREDESCI | Start Date*: 2009-05-28 | |||||||||||
| Sponsor Name:Càndid Villanueva | |||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, doble-ciego, controlado con placebo, sobre la eficacia del tratamiento con beta-bloqueantes pra aprevenir la descompenzación de la cirrosis con hipertensión po... | |||||||||||||
| Medical condition: Cirrosis hepática con hipertensión portal clínicamente significativa (mayor o igual a 10 mm Hg) sin descompensaciones como varíces esofágicas, ascitis, o encefalopatía hepática. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012592-10 | Sponsor Protocol Number: 09-057 | Start Date*: 2009-07-23 | |||||||||||
| Sponsor Name:CHU Caen | |||||||||||||
| Full Title: Méthode d’évaluation de l’aptitude à la conduite chez des patients souffrant de pathologies de l’éveil: cirrhose avec ou sans encéphalopathie (AutoSoP "foie"). | |||||||||||||
| Medical condition: cirrhose | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012919-17 | Sponsor Protocol Number: P071220 | Start Date*: 2009-11-12 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude multicentrique randomisée en double insu des effets de l'administration de norfloxacine ou d'un placebo sur la survie des malades atteints de cirrhose avec une insuffisance hépatocellulaire | |||||||||||||
| Medical condition: Malades atteints de cirrhose avec une insuffisance hépatocellulaire de grade C de Child-Pugh | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024306-36 | Sponsor Protocol Number: 1 | Start Date*: 2011-04-07 | ||||||||||||||||
| Sponsor Name:Västra Götalandsregionen | ||||||||||||||||||
| Full Title: An exploratory study of sorafenib for patients listed for transplantation due to HCC | ||||||||||||||||||
| Medical condition: Patients >18 years with hepatocellular carcinoma, on waiting list for liver transplantation | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001690-62 | Sponsor Protocol Number: HE2016 | Start Date*: 2014-09-16 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: A randomised phase II clinical trial of conditioning cyclophosphamide and chemoembolisation with or without vaccination with dendritic cells pulsed with HepG2 lysate ex vivo in patients with Hepato... | |||||||||||||
| Medical condition: Hepatocellular carcinoma | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004708-20 | Sponsor Protocol Number: RIFSYS | Start Date*: 2014-03-27 | ||||||||||||||||
| Sponsor Name:King's College London [...] | ||||||||||||||||||
| Full Title: A placebo controlled single centre double blind randomised trial to investigate the efficacy of rifaximin versus placebo in improving systemic inflammation and neutrophil malfunction in patients wi... | ||||||||||||||||||
| Medical condition: Cirrhosis and chronic hepatic encephalopathy | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-001985-86 | Sponsor Protocol Number: JX594-HEP024 | Start Date*: 2016-09-29 | |||||||||||
| Sponsor Name:SillaJen Inc. | |||||||||||||
| Full Title: A Phase 3 Randomized, Open-Label Study Comparing Pexa-Vec (Vaccinia GM-CSF / Thymidine Kinase-Deactivated Virus) Followed by Sorafenib Versus Sorafenib in Patients with Advanced Hepatocellular Carc... | |||||||||||||
| Medical condition: Advanced Hepatocellular Carcinoma (HCC) without prior systemic therapy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) PT (Prematurely Ended) PL (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017080-41 | Sponsor Protocol Number: GWMD09112 | Start Date*: 2010-04-19 | |||||||||||
| Sponsor Name:GW Pharma Ltd. | |||||||||||||
| Full Title: A randomised, partially-blind, placebo-controlled, pilot, dose-ranging study to assess the effect of cannabidiol (CBD) on liver fat levels in subjects with fatty liver disease. | |||||||||||||
| Medical condition: Subjects with fatty liver disease (≥ 5% liver fat levels). | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003561-38 | Sponsor Protocol Number: APHP220729 | Start Date*: 2023-08-23 | |||||||||||
| Sponsor Name:Assistance publique - Hôpitaux de Paris | |||||||||||||
| Full Title: Durvalumab/Tremelimumab in neoadjuvant and adjuvant setting in patients with HCC treated by electroporation ablation in curative intent: French multicenter phase 2 therapeutic DUMELEP trial (DUMELEP) | |||||||||||||
| Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001983-31 | Sponsor Protocol Number: GT-031 | Start Date*: 2021-05-04 | ||||||||||||||||
| Sponsor Name:Galectin Therapeutics Inc. | ||||||||||||||||||
| Full Title: A Seamless, Adaptive, Phase 2b/3, Double-Blind, Randomized, Placebo-controlled, Multicenter, International Study Evaluating the Efficacy and Safety of Belapectin (GR MD-02) for the Prevention of Es... | ||||||||||||||||||
| Medical condition: Esophageal Varices in NASH Cirrhosis | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-001381-42 | Sponsor Protocol Number: IMMULAB | Start Date*: 2019-01-25 | |||||||||||
| Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH am Krankenhaus Nordwest | |||||||||||||
| Full Title: IMMULAB – A phase II trial of immunotherapy with pembrolizumab in combination with local ablation for patients with early stage hepatocellular carcinoma (HCC) | |||||||||||||
| Medical condition: early stage hepatocellular carcinoma (HCC) | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (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 | |||||||||||||
|
|||||||||||||
| 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: 2012-005730-11 | Sponsor Protocol Number: K419 | Start Date*: 2015-02-11 |
| Sponsor Name:KRANKENHAUS SALEM DER EVANG. STADTMISSION HEIDELBERG GGMBH | ||
| Full Title: Effect of Clomethiazole (Distraneurin®) on CYP2E1 Activity, transaminases, Liver fat content, and liver stiffness during Alcohol Detoxification – a pilot Study | ||
| Medical condition: Alcoholic liver disease in patients hospitalised for alcohol detoxification. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001001-91 | Sponsor Protocol Number: XL184-309 | Start Date*: 2013-08-12 | |||||||||||
| Sponsor Name:Exelixis, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Controlled Study of Cabozantinib (XL184) vs Placebo in Subjects with Hepatocellular Carcinoma Who Have Received Prior Sorafenib. | |||||||||||||
| Medical condition: Subjects with Hepatocellular Carcinoma | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) IT (Completed) DE (Completed) NL (Ongoing) ES (Completed) IE (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004882-26 | Sponsor Protocol Number: ND-L02-s0201-002 | Start Date*: 2015-03-25 | |||||||||||
| Sponsor Name:Nitto Denko Corporation | |||||||||||||
| Full Title: A Phase 1b/2, Open Label, Randomized, Repeat Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, Biological Activity and Pharmacokinetics of ND L02 s0201 Injection, a Vitamin A-couple... | |||||||||||||
| Medical condition: Moderate to extensive progressive hepatic fibrosis (METAVIR F3-4) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002347-28 | Sponsor Protocol Number: 62202-255 | Start Date*: 2013-08-21 |
| Sponsor Name:ACROSS: Associació Catalana per a la Recerca Oncològica i les seves implicacions sanitàries i Socials | ||
| Full Title: Phase II interventional trial for the assessment of histological responses in all resected colorectal cancer liver metastases after preoperative cetuximab-based chemotherapy. | ||
| Medical condition: Metastatic colorectal cancer in patients resectable or potentially resectable KRAS wild. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| 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 | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-003094-21 | Sponsor Protocol Number: 2831 | Start Date*: 2021-02-11 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Strategy Option in Combined locoregional treatment (Strategy CHemoEMbolization & Ablation) of patients with hepatocellular carcinoma: A Non-inferiority Randomized Multicenter Trial | |||||||||||||
| Medical condition: Uninodular or multinodular (maximum 3 nodules) HCC with target lesion(s) = 3 cm and < 7 cm in size, not suitable for surgery, with unilobar Disease, with liver cirrhosis classified as Child-Pugh sc... | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002332-17 | Sponsor Protocol Number: RL06/7640 | Start Date*: 2007-04-18 |
| Sponsor Name:The Leeds Teaching Hospitals NHS Trust | ||
| Full Title: Prospective, randomised trial comparing the use of Tisseel versus no fibrin sealant in preventing postoperative fluid complications following liver resection | ||
| Medical condition: Patients who are undergoing liver resection. The surgery can be performed for any reason: usually primary or secondary carcinoma but may be performed for other non malignant abnormality or liver di... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.