- Trials with a EudraCT protocol (185)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
185 result(s) found for: Acute hepatitis.
Displaying page 1 of 10.
EudraCT Number: 2014-002264-33 | Sponsor Protocol Number: AH01 | Start Date*: 2014-08-25 | |||||||||||
Sponsor Name:Ole Hamberg | |||||||||||||
Full Title: Rifaximin in alcoholic hepatitis: effects on inflammatory and metabolic markers. | |||||||||||||
Medical condition: Alcoholic hepatitis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002221-37 | Sponsor Protocol Number: PA-IT72-2012 | Start Date*: 2018-11-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA POLICLINICO “PAOLO GIACCONE” DI PALERMO | |||||||||||||
Full Title: Glecaprevir/ pibrentasvir plus fixed-dose combination for 6 weeks in patients with acute hepatitis C virus: a pilot study. | |||||||||||||
Medical condition: Acute HCV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000515-80 | Sponsor Protocol Number: RIFA-AAH | Start Date*: 2012-08-29 | |||||||||||
Sponsor Name:Juan Córdoba | |||||||||||||
Full Title: Effects of rifaximin administration in patients with severe acute alcoholic hepatitis. Comparative pilot study. | |||||||||||||
Medical condition: Acute alcoholic hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000699-91 | Sponsor Protocol Number: RACHE | Start Date*: 2015-09-14 | |||||||||||
Sponsor Name:Fundació Hospital Vall Hebron Institut de Recerca | |||||||||||||
Full Title: Two treatment strategies with Ribavirin for Chronic Hepatitis E and severe acute forms randomized study | |||||||||||||
Medical condition: Chronic Hepatitis E | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005987-94 | Sponsor Protocol Number: GAHB-Study | Start Date*: 2006-07-17 | |||||||||||
Sponsor Name:University of Leipzig | |||||||||||||
Full Title: Double-blind placebo-controlled randomised trial of lamivudine in the treatment of acute hepatitis B | |||||||||||||
Medical condition: Acute Hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002837-19 | Sponsor Protocol Number: RD-5103-037-05 | Start Date*: 2007-04-16 | |||||||||||
Sponsor Name:DERBY HOSPITALS NHS FOUNDATION TRUST | |||||||||||||
Full Title: A DOUBLE BLIND PLACEBO CONTROLLED TRIAL OF TERLIPRESSIN IN THE MANAGEMENT OF SEVERE ALCOHOLIC HEPATITIS – A PRELIMINARY STUDY | |||||||||||||
Medical condition: Severe alcoholic hepatitis as judged by a Maddrey score >32 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005023-18 | Sponsor Protocol Number: V232-054-00 | Start Date*: 2005-06-09 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: Study in Healthy Young Adults to Assess the Safety, Tolerability, and Immunogenicity of a Recombinant Hepatitis B Vaccine Manufactured by a Process Upgrade | |||||||||||||
Medical condition: Acute hepatitis B without delta-agent and without hepatic coma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021716-42 | Sponsor Protocol Number: 1220.30 | Start Date*: 2011-03-11 | |||||||||||
Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||
Full Title: A phase III, randomised, double-blind and placebo-controlled study of once daily BI 201335 120 mg for 12 or 24 weeks or BI 201335 240 mg for 12 weeks in combination with pegylated interferon-α and ... | |||||||||||||
Medical condition: genotype 1 chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) BE (Completed) GB (Completed) DE (Completed) ES (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001081-42 | Sponsor Protocol Number: HepNet-aHCV-IV | Start Date*: 2014-10-21 | |||||||||||||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||||||||||||
Full Title: Interferon-free Treatment of Acute Genotype 1 Hepatitis C Virus Infection with Ledipasvir/Sofosbuvir Fixed-Dose Combination - The HepNet Acute HCV IV Study | |||||||||||||||||||||||
Medical condition: Adults with acute genotype 1 hepatitis C virus (HCV) infection | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015002-19 | Sponsor Protocol Number: VTI-206 | Start Date*: 2010-01-18 | |||||||||||
Sponsor Name:VITAL THERAPIES INCORPORATED | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ELAD IN SUBJECTS WITH ACUTE ON CHRONIC HEPATITIS (AOCH) | |||||||||||||
Medical condition: Acute on Chronic Hepatitis (AOCH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001884-21 | Sponsor Protocol Number: VTI-210 | Start Date*: 2013-07-26 | |||||||||||
Sponsor Name:VITAL THERAPIES INCORPORATED | |||||||||||||
Full Title: A RANDOMIZED, OPEN-LABEL, MULTICENTER, CONTROLLED STUDY TO ASSESS SAFETY AND EFFICACY OF ELAD IN SUBJECTS WITH SEVERE ACUTE ALCOHOLIC HEPATITIS (SAAH) AND LILLE SCORE FAILURE | |||||||||||||
Medical condition: Severe Acute Alcoholic Hepatitis (sAAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001213-17 | Sponsor Protocol Number: MYR301 | Start Date*: 2019-08-24 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Multicenter, Open-label, Randomized Phase 3 Clinical Study to Assess Efficacy and Safety of Bulevirtide in Patients with Chronic Hepatitis Delta | |||||||||||||
Medical condition: Chronic Hepatitis Delta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004665-33 | Sponsor Protocol Number: VX06-950-106 | Start Date*: 2007-04-04 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2 Study of Telaprevir (VX-950) in Combination with Peginterferon Alfa-2a (Pegasys®), and Ribavirin (Copegus®) in Subjects with Genotype 1 Hepatitis C Who Have Not Achieved Sustained Viral R... | |||||||||||||
Medical condition: Hepatitis C virus (HCV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001485-15 | Sponsor Protocol Number: MYR204 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Gilead Sciences Inc. | |||||||||||||
Full Title: A Multicenter, Open-label, Randomized Phase 2b Clinical Study to Assess Efficacy and Safety of Bulevirtide in Combination with Pegylated Interferon alfa-2a in Patients with Chronic Hepatitis Delta | |||||||||||||
Medical condition: Chronic Hepatitis Delta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004812-12 | Sponsor Protocol Number: GS-US-337-1612 | Start Date*: 2015-05-07 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: Open-Label Study to Evaluate the Safety and Efficacy of Ledipasvir/Sofosbuvir (LDV/SOF) Fixed-Dose Combination (FDC) for 6 Weeks in Subjects with Acute Genotype 1 or 4 Hepatitis C Virus (HCV) and C... | ||||||||||||||||||
Medical condition: Acute Genotype 1 or Genotype 4 Hepatitis C Virus Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004902-85 | Sponsor Protocol Number: ABI-H2158-201 | Start Date*: 2020-10-30 | |||||||||||
Sponsor Name:Assembly Biosciences | |||||||||||||
Full Title: A Phase 2a, Multicenter, Single-Blind, Placebo-Controlled, Multiple Cohort Study Evaluating ABI-H2158-Containing Regimens in Chronic Hepatitis B Infection | |||||||||||||
Medical condition: Chronic Hepatitis B Infection | |||||||||||||
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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: 2016-001125-13 | Sponsor Protocol Number: SAHIV-IMEA50 | Start Date*: 2017-04-07 | |||||||||||
Sponsor Name:IMEA (Institut de Médecine et d’Epidémiologie Appliquée)–Fondation Léon M’Ba | |||||||||||||
Full Title: Pilot study - Short duration therapy of acute hepatitis C genotypes 1 or 4 in HIV-infected patients: efficacy and tolerability of grazoprevir 100mg/elbasvir 50mg during 8 weeks | |||||||||||||
Medical condition: Acute hepatitis C (genotypes 1 or 4) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003836-39 | Sponsor Protocol Number: VX08-950-111 | Start Date*: 2008-11-16 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Randomized Study of Stopping Treatment at 24 Weeks or Continuing Treatment to 48 Weeks in Treatment-Naïve Subjects with Genotype 1 Chronic Hepatitis C who Achieve an Extended Rapid Viral Response... | |||||||||||||
Medical condition: Hepatitis C Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001044-44 | Sponsor Protocol Number: VX-950-TiDP24-C208 | Start Date*: 2007-08-01 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A Phase IIa randomized, open-label study of telaprevir (VX-950) administered every 12 or every 8 hours in combination with either Peg-IFN alfa2a (Pegasys®) and ribavirin (Copegus®) or Peg-IFN alfa2... | |||||||||||||
Medical condition: Hepatitis C infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003474-27 | Sponsor Protocol Number: HepNet-aHCV-V | Start Date*: 2019-03-11 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: Multicenter trial for the treatment of acute Hepatitis C for 8 weeks with Sofosbuvir/Velpatasvir fix dose combination - The HepNet Acute HCV-V study | |||||||||||||
Medical condition: Adults with acute hepatitis C virus (HCV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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