- Trials with a EudraCT protocol (1,495)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,495 result(s) found for: Hepatitis A.
Displaying page 2 of 75.
EudraCT Number: 2007-000328-42 | Sponsor Protocol Number: CP-104 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:Arrow Therapeutics Ltd | |||||||||||||
Full Title: A clinical pharmacology study to determine the pharmacokinetic , safety and tolerability profile and antiviral activity of multiple oral doses of A-831 in otherwise healthy male Hepatitis C carrie... | |||||||||||||
Medical condition: Male Hepatitis C carriers with compensated liver disease | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001639-23 | Sponsor Protocol Number: V232-058 | Start Date*: 2006-09-05 | |||||||||||
Sponsor Name:Merck SHARP & DOHME DE ESPAÑA | |||||||||||||
Full Title: A Study to Assess the Anamnestic Immune Response 4 to 6 Years After a Primary Vaccination Series With HBVAXPRO™ Estudio para evaluar la respuesta inmune anamnésica 4 a 6 años después de una pauta d... | |||||||||||||
Medical condition: Hepatitis B | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000840-10 | Sponsor Protocol Number: KB 036 | Start Date*: 2005-09-19 | |||||||||||
Sponsor Name:KEDRION | |||||||||||||
Full Title: Open Label Phase II Multicenter Study for the Evaluation of Pharmacokinetics of VENBIG (Human Immunoglobulin anti-Hepatitis B for Intravenous Use) and IMMUNOHBS (Human Immunoglobulin anti Hepatitis... | |||||||||||||
Medical condition: Prevention of hepatitis B recurrence after liver transplantation in patients who carry the surface antigen of the hepatitis B virus. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000571-16 | Sponsor Protocol Number: GS-US-334-0109 | Start Date*: 2012-09-21 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
Full Title: An Open-Label Study of GS-7977+ Ribavirin for 12 Weeks in Subjects with Chronic HCV Infection who Participated in Prior Studies Evaluating GS-7977. | ||||||||||||||||||
Medical condition: Chronic Genotype 2 or 3 HCV Infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) GB (Completed) SE (Completed) EE (Completed) DE (Completed) NL (Completed) ES (Completed) PL (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000336-25 | Sponsor Protocol Number: ML18675 | Start Date*: 2005-04-12 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Longitudinal analysis of HBV-specific T cell responses in patients with HBeAg-negative chronic hepatitis B (CHB) treated with pegylated interferon alfa-2a (40 KD) (PEGASYS, Ro 25-8310). Immuno... | |||||||||||||
Medical condition: chronic hepatitis B, HBeAg-negative | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003446-27 | Sponsor Protocol Number: TMC435HPC3021 | Start Date*: 2015-01-02 | |||||||||||
Sponsor Name:Janssen R&D Ireland | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Single-Arm Study to Investigate the Efficacy and Safety of a 12-Week Regimen of Simeprevir in Combination with Sofosbuvir in Treatment-Naïve or -Experienced Subj... | |||||||||||||
Medical condition: Hepatitis C-Infection genotype 4 Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003879-18 | Sponsor Protocol Number: SOF-VEL/PED/2020 | Start Date*: 2021-04-21 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: Treatment of chronic hepatitis C in children aged 6 – 18 years using a pangenotypic direct-acting antiviral (sofosbuvir/velpatasvir) | |||||||||||||
Medical condition: Chronic hepatitis C | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001744-53 | Sponsor Protocol Number: PAI study | Start Date*: 2008-04-02 | ||||||||||||||||
Sponsor Name:University of Leipzig | ||||||||||||||||||
Full Title: Open, randomized study for evaluation of an active Hepatitis B vaccination(HBVAXPRO) in combination with a passive immunisation with Hepatitis B immunoglobulins (Hepatect) for subjects, who did not... | ||||||||||||||||||
Medical condition: Hepatitis B immunization | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000257-36 | Sponsor Protocol Number: MI2- CORONA-2007 | Start Date*: 2008-02-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Double blind, randomized, clinical trial to evaluate efficacy and safety of Phyllanthus amarus versus placebo in the treatment of patients with chronic hepatitis B | |||||||||||||
Medical condition: Chronic hepatitis B | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002139-94 | Sponsor Protocol Number: IPH1101-203 | Start Date*: 2007-06-19 | |||||||||||
Sponsor Name:Innate Pharma | |||||||||||||
Full Title: Multiple dose Phase II study of IPH1101 in monotherapy or associated with a low dose of IL2 (2MIU) in non previously treated hepatitis C patients | |||||||||||||
Medical condition: Non previously treated Hepatitis C patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004138-41 | Sponsor Protocol Number: TEL-PR | Start Date*: 2012-12-10 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PARMA | |||||||||||||
Full Title: Anti-viral T cell responses in patients with chronic HCV infection treated with telaprevir: can therapy induce functional T cell reconstitution? | |||||||||||||
Medical condition: Chronic active hepatitis C never treated previously with anti-HCV therapies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002608-19 | Sponsor Protocol Number: 64294178HPC3001 | Start Date*: 2017-06-29 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Prospective 3-Year Follow-up Study in Subjects Treated in a Preceding Phase 2 or 3 Study With a Regimen Containing Odalasvir and AL-335 With or Without Simeprevir for the Treatment of Hepatitis C... | |||||||||||||
Medical condition: Chronic Hepatitis C virus infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001130-13 | Sponsor Protocol Number: | Start Date*: 2007-12-05 | |||||||||||
Sponsor Name:Malmö University Hospital | |||||||||||||
Full Title: Hepatitis C in a cohort of patients with maintenance therapy for opiate dependence - prevalence, severity and outcome of antiviral therapy | |||||||||||||
Medical condition: Hepatitis C | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002459-33 | Sponsor Protocol Number: MEN_BOC | Start Date*: 2011-12-06 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Boceprevir in Combination With Peginterferon Alfa-2b and Ribavirin in Difficult-to-Treat Menopausal Women With Chronic Hepatitis C Genotype 1, either deemed Nonresponders to Peginterferon/Ribavirin... | |||||||||||||
Medical condition: menopausal women with chronic HCV genotype1, naive or previously treated her with standard antiviral therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003737-40 | Sponsor Protocol Number: 958 | Start Date*: 2006-05-03 | |||||||||||
Sponsor Name:Biotest AG | |||||||||||||
Full Title: An open, prospective, randomised parallel study investigating efficacy and safety of the human hepatitis B immunoglobulin BT088 after subcutaneous or intramuscular application in liver transplanted... | |||||||||||||
Medical condition: long-term prophylaxis against hepatitis B re-infection ≥ 3 months after liver transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004674-42 | Sponsor Protocol Number: GS-US-334-1113 | Start Date*: 2015-11-20 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Long Term Follow-up Registry for Adolescent and Pediatric Subjects Who Received a Gilead Hepatitis C Virus Direct Acting Antiviral (DAA) in Gilead-Sponsored Chronic Hepatitis C Infection Trials | ||||||||||||||||||
Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002985-39 | Sponsor Protocol Number: ML18253 | Start Date*: 2004-12-13 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A multicenter, randomized, controlled study comparing the efficacy and safety of 48 weeks of 40kD branched pegylated interferon alfa-2a (PEGASYS, Ro 25-8310) versus 96 weeks of PEGASYS, alone or in... | |||||||||||||
Medical condition: Treatment of chronic hepatitis B, HBeAg-negative | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000416-25 | Sponsor Protocol Number: TMC435-TiDP16-C213 | Start Date*: 2011-09-02 | |||||||||||
Sponsor Name:Janssen R&D Ireland | |||||||||||||
Full Title: A Phase III, open-label trial of TMC435 in combination with peginterferon alpha-2a and ribavirin for HCV genotype-1 infected subjects who participated in the placebo group of a Phase II/III TMC435 ... | |||||||||||||
Medical condition: Hepatitis C Virus (HCV) genotype-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) ES (Completed) AT (Completed) PT (Completed) NL (Completed) DE (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006803-35 | Sponsor Protocol Number: CABF656A2201 | Start Date*: 2008-02-21 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An open-label, randomized, multicenter, active-controlled, dose-ranging study to evaluate the safety and efficacy of albinterferon alfa-2b administered every 4 weeks plus ribavirin in interferon al... | |||||||||||||
Medical condition: CHONIC HEPATITIS C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004713-24 | Sponsor Protocol Number: GECOMstudy | Start Date*: 2016-04-11 | ||||||||||||||||
Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | ||||||||||||||||||
Full Title: A Multicenter, Open Label, Pilot Study to Investigate Tolerability and Efficacy of MK5172 (Grazoprevir) / MK8742 (Elbasvir) Without Ribavirin for 12 Weeks in Patients With Chronic HCV G1b Infection... | ||||||||||||||||||
Medical condition: Chronic infection with Hepatitis C virus genotype 1b with compensated cirrhosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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