- 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 A.
Displaying page 8 of 75.
| EudraCT Number: 2010-020033-14 | Sponsor Protocol Number: CDEB025A2210 | Start Date*: 2010-09-03 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A multicentre, randomized, double-blind, placebocontrolled, parallel-group phase II study on efficacy and safety of DEB025 combined with peg-IFN alfa-2a and ribavirin in chronic hepatitis C genotyp... | |||||||||||||
| Medical condition: Chronic Hepatitis C Genotype 1 patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) HU (Completed) DE (Completed) FR (Completed) ES (Completed) BE (Completed) IT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012579-90 | Sponsor Protocol Number: 1220.40 | Start Date*: 2009-08-04 | |||||||||||||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||||||||||||
| Full Title: Antiviral effect and safety of once daily BI 201335 NA in hepatitis C virus genotype 1 infected treatment-naïve patients for 12 or 24 weeks as combination therapy with pegylated interferon-α 2a and... | |||||||||||||||||||||||
| Medical condition: chronic hepatitis C | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) FR (Completed) AT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-003593-85 | Sponsor Protocol Number: VX-950HPC3005 | Start Date*: 2012-04-26 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: Multicenter, Open-Label Study of Telaprevir in Combination With Peginterferon Alfa and Ribavirin in Human Immunodeficiency Virus/Genotype 1 Chronic Hepatitis C Coinfected Subjects With Severe Fibro... | |||||||||||||
| Medical condition: Chronic hepatitis C infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) IT (Completed) AT (Completed) DE (Completed) GB (Completed) PT (Completed) HU (Completed) IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002771-33 | Sponsor Protocol Number: MK3034-113-00 | Start Date*: 2012-12-22 | |||||||||||
| Sponsor Name:MSD ITALIA S.R.L. | |||||||||||||
| Full Title: An open label study assessing SVR and Viral Resistance profile with Boceprevir plus PEG-IFN plus Ribavirin triple therapy in HCV-1 infected patients with insulin resistance who have failed PEG-IFN ... | |||||||||||||
| Medical condition: HCV-1 with insulin resistance | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021337-31 | Sponsor Protocol Number: TMC435-TiDP16-C212 | Start Date*: 2011-11-03 | |||||||||||
| Sponsor Name:Janssen R&D Ireland | |||||||||||||
| Full Title: A Phase III open-label study to evaluate the safety, tolerability and efficacy of TMC435 plus PegIFNα-2a (Pegasys) and ribavirin (Copegus) triple therapy in chronic hepatitis C genotype-1 infected ... | |||||||||||||
| Medical condition: Hepatitis C and co-infected with HIV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001682-27 | Sponsor Protocol Number: GS-US-342-1140 | Start Date*: 2014-08-19 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks with Sofosbuvir and Ribavirin for 24 Weeks in Subje... | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IT (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-012344-17 | Sponsor Protocol Number: CICL670AIT06T | Start Date*: 2009-10-13 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
| Full Title: A randomized, open label, single center, phase IIa controlled trial to assess tolerability, safety and effect of treatment with deferasirox plus standard antiviral therapy versus standard antivira... | |||||||||||||
| Medical condition: Chronic hepatitis C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012459-96 | Sponsor Protocol Number: CIN-VHC-01 | Start Date*: 2010-06-08 | |||||||||||
| Sponsor Name:Dr Calleja Panero | |||||||||||||
| Full Title: VALORACIÓN INTENSIVA DE LA CINÉTICA DEL RNA DEL VIRUS DE LA HEPATITIS C COMO PREDICTOR PRECOZ DE AUSENCIA DE RESPUESTA VIROLÓGICA SOSTENIDA EN PACIENTES CON HEPATITIS CRÓNICA POR VHC TRATADOS CON I... | |||||||||||||
| Medical condition: HEPATITIS C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-007296-24 | Sponsor Protocol Number: 08/01 | Start Date*: 2009-01-21 | |||||||||||
| Sponsor Name:AISF - ASSOCIAZIONE ITALIANA PER LO STUDIO DEL FEGATO | |||||||||||||
| Full Title: Multicenter open-label, phase IIB study with 0.5 mg / day Entecavir (BARACLUDE ) in patients with positive HBsAg solid or hematologic malignancies undergoing chemotherapy (ChemET) (ChemET) | |||||||||||||
| Medical condition: Subject with new diagnosis of solid or haematological cancer in inactive carrier in chronic virus B infected patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000923-33 | Sponsor Protocol Number: HepB/APAP/2011 | Start Date*: 2011-07-14 | ||||||||||||||||
| Sponsor Name:Rijksinstituut voor Volksgezondheid en Milieu (RIVM) | ||||||||||||||||||
| Full Title: Effects of paracetamol use on the immune response after hepatitis B vaccination | ||||||||||||||||||
| Medical condition: No medical conditions will be studied. The association between timing of the use of paracetamol during hepatitis B vaccination and the development of an antibody response will be studied in student... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-005448-17 | Sponsor Protocol Number: TMC435HPC1010 | Start Date*: 2015-04-09 | |||||||||||
| Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
| Full Title: A Phase 1, open-label, randomized, 2-panel, 3-way crossover study in healthy adult subjects to assess the relative bioavailability of simeprevir following single dose administration of age-appropri... | |||||||||||||
| Medical condition: Chronic Hepatitus C Virus (HCV) Infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000557-21 | Sponsor Protocol Number: HEPBARE-2015-01 | Start Date*: 2015-06-12 | ||||||||||||||||||||||||||
| Sponsor Name:Vall de Hebron Hospital | ||||||||||||||||||||||||||||
| Full Title: Immunogenicity and efficacy of the vaccine against Hepatitis B virus in immunosuppressed patients antiHBc positive with low titers of anti-HBs. Assessment of clinical usefulness in preventing react... | ||||||||||||||||||||||||||||
| Medical condition: Patients under immunosuppressant therapy with past hepatitis B infection (HBsAg -/antiHBc +) but low antiHBs titers. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-001050-16 | Sponsor Protocol Number: GS-US-330-1508 | Start Date*: 2016-06-23 | |||||||||||
| Sponsor Name:GILEAD SCIENCES INCORPORATED | |||||||||||||
| Full Title: A Long Term Follow-up Registry of Subjects Treated in A Gilead-Sponsored Trial in Subjects with Chronic Hepatitis B Infection. | |||||||||||||
| Medical condition: Chronic Hepatitis B virus infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004556-71 | Sponsor Protocol Number: P05514 | Start Date*: 2009-05-25 | ||||||||||||||||||||||||||
| Sponsor Name:Schering-Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
| Full Title: Estudio de un solo grupo para facilitar tratamiento con boceprevir a sujetos con el genotipo 1 del virus de la hepatitis C crónica que no han respondido a peginterferón/ribavirina en estudios previ... | ||||||||||||||||||||||||||||
| Medical condition: Hepatitis C Crónica | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Completed) FR (Completed) DE (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2017-001024-21 | Sponsor Protocol Number: nc5317 | Start Date*: 2018-02-23 | ||||||||||||||||
| Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | ||||||||||||||||||
| Full Title: innovative model for the eradication of HCV in a population at high risk of irregular immigrants and low-income refugees | ||||||||||||||||||
| Medical condition: Chronic HCV hepatitis, all fibrosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-004939-39 | Sponsor Protocol Number: GS-EU-174-1403 | Start Date*: 2015-05-26 | |||||||||||
| Sponsor Name:Gilead Sciences International Ltd. | |||||||||||||
| Full Title: Pharmacoepidemiology study to define the long-term safety profile of tenofovir disoproxil fumarate (Tenofovir DF, Viread®) and describe the management of Tenofovir DF-associated renal and bone toxi... | |||||||||||||
| Medical condition: Chronic Hepatitis B | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Prematurely Ended) ES (Prematurely Ended) BG (Prematurely Ended) GR (Completed) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003650-20 | Sponsor Protocol Number: V232-060-02 | Start Date*: 2007-02-19 | |||||||||||
| Sponsor Name:Merck & Co Inc., | |||||||||||||
| Full Title: A Study in Renal Predialysis and Dialysis Patients of the Safety, Tolerability, and Immunogenicity of Recombinant Hepatitis B Vaccine Manufactured with a Modified Process | |||||||||||||
| Medical condition: Hepatitis B | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002446-23 | Sponsor Protocol Number: GS-US-342-1143 | Start Date*: 2017-01-19 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 2, Open-Label, Multicenter, Multi-cohort Study to Investigate the Safety and Efficacy of Sofosbuvir/Velpatasvir in Adolescents and Children with Chronic HCV Infection | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) BE (Completed) Outside EU/EEA IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-003950-10 | Sponsor Protocol Number: 116722 | Start Date*: 2013-04-16 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: An open, phase IV, single-group, multicentre study to assess the long-term persistence of antibodies against hepatitis B and the immune response to a challenge dose of Engerix™-B Kinder in adolesce... | |||||||||||||
| Medical condition: Hepatitis | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004564-30 | Sponsor Protocol Number: VX11-950-118 | Start Date*: 2013-02-12 | |||||||||||
| Sponsor Name:Vertex Pharmaceuticals | |||||||||||||
| Full Title: A Two-Part, Open-Label, Single-Arm Phase 1/2 Study of Safety, Pharmacokinetics, and Efficacy of Telaprevir in Combination With Peginterferon alfa-2b and Ribavirin in Pediatric Subjects Aged 3 to 17... | |||||||||||||
| Medical condition: genotype 1 Hepatitis C Virus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) BE (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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