- Trials with a EudraCT protocol (1,498)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,498 result(s) found for: Hepatitis.
Displaying page 29 of 75.
| EudraCT Number: 2005-002455-41 | Sponsor Protocol Number: | Start Date*: 2006-02-15 |
| Sponsor Name:Karolinska Institutet | ||
| Full Title: Clinical, morphological and biochemical effects of antioxidant treatment of patients with chronic hepatitis C. | ||
| Medical condition: Chronic hepatitis C with moderate to severe liver damage. The patients should not be suitable for standard medical treatment or refuse standard medical treatment for personal reasons. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002351-34 | Sponsor Protocol Number: V1.0 | Start Date*: 2013-02-21 |
| Sponsor Name:Medizinische Universitaet Wien, Univ.Klinik f.Innere Medizin III, Abteilung fuer Gastroenterologie und Hepatologie | ||
| Full Title: Effects of oral and intravenous lipid load on Hepatitis C virus concentrations in serum and lipoprotein subfractions | ||
| Medical condition: chronic hepatitis C | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003534-17 | Sponsor Protocol Number: 1241.30 | Start Date*: 2013-04-05 |
| Sponsor Name:Boehringer Ingelheim España S.A | ||
| Full Title: A phase II randomised, double-blind and placebo-controlled study of BI 207127 in combination with faldaprevir and ribavirin in patients with moderate hepatic impairment (Child-Pugh B) with genotype... | ||
| Medical condition: Chronic Hepatitis C Infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) DE (Completed) GB (Prematurely Ended) IT (Prematurely Ended) IE (Prematurely Ended) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005816-26 | Sponsor Protocol Number: AI463-028 | Start Date*: 2007-08-30 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: Evaluation of the Pharmacokinetics, Safety, Tolerability and Efficacy of Entecavir (ETV) in Pediatric Subjects with Chronic Hepatitis B Virus (HBV) Infection who are HBeAg-Positive. Revised Pro... | |||||||||||||
| Medical condition: Chronic Hepatitis B Virus (HBV) Infection | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002413-11 | Sponsor Protocol Number: PRI01C | Start Date*: 2012-02-07 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur MSD S.N.C | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase III open-label randomised study, to evaluate the immunogenicity and safety of the concomitant administration of V419 (PR5I) given at 2, 3 and 4 months of age with two types of meningococcal... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: PR5I is developed to provide active immunization against diphtheria, tetanus, pertussis, poliomyelitis (caused by poliovirus Types 1, 2 and 3), invasive disease caused by Haemophilus influenza ty... | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-003538-11 | Sponsor Protocol Number: 1220.5 | Start Date*: 2008-10-01 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: Antiviral effect, safety and pharmacokinetics of BI 201335 NA in hepatitis C virus genotype 1 infected treatment-naïve and treatment-experienced patients for 24 weeks as combination therapy with pe... | |||||||||||||
| Medical condition: chronic hepatitis C infection of genotype 1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) FR (Completed) NL (Completed) PT (Completed) GB (Completed) AT (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002171-33 | Sponsor Protocol Number: HEPVACHIV | Start Date*: 2005-09-14 |
| Sponsor Name:Aalborg Sygehus Syd | ||
| Full Title: Hepatitis vaccination til patienter med HIV infektion. Betydning af adjuverende interleukin-2 | ||
| Medical condition: Patienter med Hiv infektion har øget risiko for hepatitis A og hepatitis B. Sundhedsmyndigheder anbefaler vaccination. Effekt er imidlertid mindre end for raske personer. Forsøget tester om adjuver... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001344-22 | Sponsor Protocol Number: 116640 | Start Date*: 2013-02-19 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase II, randomised, single-blind study to develop read-outs aimed at detecting and characterising the early and adaptive immune responses and to evaluate the kinetics of the early response and ... | ||
| Medical condition: Healthy volunteers (Hepatitis B surface antigen (HBsAg) vaccine administered in hepatitis B virus (HBV) naive adult subjects aged between 18 and 45 years old, inclusive, in good general health.) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016773-15 | Sponsor Protocol Number: HepVac | Start Date*: 2010-01-13 | |||||||||||
| Sponsor Name:Matti Ristola | |||||||||||||
| Full Title: A Randomized, Controlled, Open-label Study of Comparing Immunogenicity of Sequential Hepatitis B and Hepatitis A Vaccination vs Vaccination with a Dual Hepatitis B and Hepatitis A Vaccine among HI... | |||||||||||||
| Medical condition: Immunisaatio A- ja B-hepatiittia vastaan HIV-infektoituneilla henkilöillä | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-000687-77 | Sponsor Protocol Number: 0305 | Start Date*: 2005-06-28 |
| Sponsor Name:Uni-Zentrum naturheilkunde | ||
| Full Title: Pilotstudie zur Verträglichkeit und Effektivität eines Artischockenpräparates bei Patienten mit chronischer Hepatitis C | ||
| Medical condition: chronische Hepatitis C | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-000706-36 | Sponsor Protocol Number: P05498 | Start Date*: 2008-09-30 | |||||||||||
| Sponsor Name:Hannover Medical School; Competence Network Viral Hepatitis (Hep-Net) | |||||||||||||
| Full Title: Optimization of treatment for patients with chronic hepatitis C infected with HCV-genotype 2 or 3: 12 vs. 24 weeks of treatment extension for patients without rapid virological response | |||||||||||||
| Medical condition: chronic hepatitis c infection genotype 2/3 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016635-36 | Sponsor Protocol Number: 113615 | Start Date*: 2010-03-04 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase II, open-label, randomised, multicentre study to evaluate the safety and immunogenicity of GlaxoSmithKline Biologicals’ DTPa-HBV-IPV/Hib-MenC-TT vaccine, when given to healthy infants at 2,... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Primary and booster immunisation of healthy infants in the first year of life against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis, Haemophilus influenzae type b, serogroup C meningoc... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2004-001469-16 | Sponsor Protocol Number: TPL102357 | Start Date*: 2005-10-20 |
| Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
| Full Title: A double-blind, randomized, placebo-controlled, multi-centre, dose-ranging, parallel group, phase II study to assess efficacy, safety/tolerability, and pharmacokinetics of a thrombopoietin receptor... | ||
| Medical condition: Thrombocytopenia caused by hepatitis-C | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001819-36 | Sponsor Protocol Number: Sci-B-Vac–001 | Start Date*: 2018-02-02 | |||||||||||
| Sponsor Name:VBI Vaccines Inc. | |||||||||||||
| Full Title: A Phase 3 Double-Blind Randomized Controlled Trial to Compare the Immunogenicity and Safety of a Three-dose Regimen of Sci-B-Vac™ to a Three-dose Regimen of Engerix-B® in Adults (PROTECT) | |||||||||||||
| Medical condition: Hepatitis B vaccination in healthy adults | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001956-31 | Sponsor Protocol Number: 2015-001956-31 | Start Date*: 2015-06-09 | |||||||||||
| Sponsor Name:Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre. | |||||||||||||
| Full Title: Direct acting antiviral therapy of hepatitis C in Denmark: treatment response, adverse events and resistance associated variants | |||||||||||||
| Medical condition: Patients with chronic hepatitis C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004830-81 | Sponsor Protocol Number: FIL_BArT | Start Date*: 2015-12-24 | ||||||||||||||||
| Sponsor Name:FONDAZIONE ITALIANA LINFOMI ONLUS | ||||||||||||||||||
| Full Title: A multicenter study to evaluate the anti-viral activity of an interferon-free treatment with ledipasvir/sofosbuvir (G1 and G4) and sofosbuvir/velpatasvir (G2 and G3) for patients with hepatitis C v... | ||||||||||||||||||
| Medical condition: Patients with hepatitis C virus-associated indolent B-cell lymphomas | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-002446-19 | Sponsor Protocol Number: TRIC-1 | Start Date*: 2005-09-10 |
| Sponsor Name:Hospital de Valme | ||
| Full Title: Insuline resistance treatment effect in patients with genotype 1 hepatitis C treated with peginterferon alfa-2a plus ribavirin in usual clinical practice Efecto del tratamiento de la resistencia a ... | ||
| Medical condition: Treatment effect of insuline resistance in patients with genotype 1 hepatitis C treated with peginterferon alfa 2a plus ribavirin in usual clinical practice | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005849-19 | Sponsor Protocol Number: RHM MED 0673 | Start Date*: 2006-07-06 |
| Sponsor Name:Southampton University Hospitals NHS Trust | ||
| Full Title: Finite duration treatment in pre-cirrhotic chronic hepatitis B virus (HBV) infection: Phase IV study of Lamivudine priming of Pegasys treatment in HBeAg positive patients | ||
| Medical condition: pre-cirrhotic chronic hepatitis B virus (HBV) infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001413-34 | Sponsor Protocol Number: VIHCREC01 | Start Date*: 2005-04-21 |
| Sponsor Name:Bonaventura Clotet Sala | ||
| Full Title: ESTUDIO DE UNA DOBLE ESTRATEGIA PARA INDUCIR Y EXPANDIR EL REPERTORIO DE CÉLULAS T BASADA EN LA ADMINISTRACIÓN DE HORMONA DE CRECIMIENTO Y VACUNA EN PACIENTES CON INFECCIÓN POR EL VIH 1 | ||
| Medical condition: HIV-1 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-004455-29 | Sponsor Protocol Number: 112115 | Start Date*: 2008-12-05 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase II, randomized, multicentre, observer-blind study to compare and characterize the immunoginicity and safety parameters induced by various GSK Biologicals’ Adjuvant Systems in combination wi... | ||
| Medical condition: Hepatitis B surface antigen (HBsAg) vaccine administred in HBV naïve adult subjects aged between 18 and 45 years old, inclusive, in good general health. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) DE (Completed) | ||
| Trial results: View results | ||
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