- Trials with a EudraCT protocol (757)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
757 result(s) found for: Chronic Hepatitis C AND Hepatitis C.
Displaying page 7 of 38.
| 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 | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002039-34 | Sponsor Protocol Number: CABF656B2202 | Start Date*: 2008-12-15 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| 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: chronic hepatitis C | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) FR (Completed) PL (Completed) IT (Completed) GR (Prematurely Ended) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000342-30 | Sponsor Protocol Number: MK-5172-061 | Start Date*: 2014-06-06 |
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | ||
| Full Title: A Phase III Open-Label Clinical Trial to Study the Efficacy and Safety of the Combination Regimen of MK-5172/MK-8742 in Treatment-Naïve Subjects with Chronic HCV GT1, GT4, GT5, and GT6 Infection w... | ||
| Medical condition: Hepatitis C | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001249-26 | Sponsor Protocol Number: GS-US-337-1431 | Start Date*: 2016-02-12 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Registry for Subjects with Cirrhosis Who Achieve a Sustained Virologic Response Following Treatment with a Sofosbuvir-Based Regimen without Interferon for Chronic Hepatitis C Infection in Gilead-... | ||||||||||||||||||
| Medical condition: Hepatitis C Virus Infection | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-006604-11 | Sponsor Protocol Number: NV19865 | Start Date*: 2007-12-06 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A Phase II, Randomized, Double-Blinded, Multicenter, Dose Finding Study Evaluating the Efficacy and Safety of the HCV Polymerase Inhibitor Prodrug (RO4588161) when given in combination with Pegasys... | |||||||||||||
| Medical condition: Chronic hepatitis C | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) DE (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000944-43 | Sponsor Protocol Number: GS-US-248-0120 | Start Date*: 2011-08-09 | ||||||||||||||||
| Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
| Full Title: A Phase 2 Randomized, Open-Label Study of GS-5885 Administered Concomitantly with GS-9451, Tegobuvir and Ribavirin (RBV) to Treatment-Naive Subjects with Chronic Genotype 1 HCV Infection | ||||||||||||||||||
| Medical condition: Genotype 1 Hepatitis C Virus Infection | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-002349-80 | Sponsor Protocol Number: M13-583 | Start Date*: 2015-11-13 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Single-Arm, Open-Label Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults with Chronic Hepatitis C Virus Genotype 4, 5, or 6 Infection (ENDURANCE-4) | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Genotype 4, 5 or 6 Infection | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Completed) BE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005293-31 | Sponsor Protocol Number: AI452-016 | Start Date*: 2012-06-01 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Long-Term Follow-Up Study of Subjects Who Participated in a Clinical Trial in which Peginterferon Lambda-1a (BMS-914143) was Administered for the Treatment of Chronic Hepatitis C Revised Proto... | |||||||||||||
| Medical condition: Chronic Hepatitis C | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) ES (Completed) PL (Completed) IT (Completed) GR (Completed) FI (Completed) BE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018146-38 | Sponsor Protocol Number: MFN09/15 | Start Date*: 2010-05-28 | |||||||||||
| Sponsor Name:Swedish Orphan International AB | |||||||||||||
| Full Title: Multicenter randomized controlled study comparing the efficacy and safety of natural Multi-subtype interferon alpha (Multiferon) in association with ribavirin versus retreatment with pegylated inte... | |||||||||||||
| Medical condition: Hepatitis C | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004810-41 | Sponsor Protocol Number: MV28073 | Start Date*: 2012-04-18 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: An international, multicenter, open-label study evaluating sustained virological response and safety with Boceprevir in triple combination therapy with Peginterferon alfa-2a (40KD) and Ribavirin in... | |||||||||||||
| Medical condition: Genotype 1 CHC virus infection | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) HU (Completed) ES (Completed) PL (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004097-29 | Sponsor Protocol Number: TMC435HPC3011 | Start Date*: 2012-01-31 | |||||||||||
| Sponsor Name:Janssen R&D Ireland | |||||||||||||
| Full Title: An Open-Label, Single-Arm Phase III Study to Evaluate the Efficacy, Safety and Tolerability of TMC435 in Combination With PegIFN alfa-2a (Pegasys) and Ribavirin (Copegus) in Treatment-Naïve or Trea... | |||||||||||||
| Medical condition: Hepatitis C Virus genotype-4 (HCV-4) in treatment-naïve or treatment-experienced subjects | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004212-64 | Sponsor Protocol Number: IMC-I109V-101 | Start Date*: 2020-08-12 | ||||||||||||||||
| Sponsor Name:Immunocore Ltd | ||||||||||||||||||
| Full Title: An Open-label Study Evaluating the Safety, Antiviral Activity, and Pharmacokinetics of IMC-I109V in HLA-A*02:01 Positive Patients with Chronic HBV who are Non-Cirrhotic, Hepatitis B e Antigen-nega... | ||||||||||||||||||
| Medical condition: chronic hepatitis B virus (HBV) infection | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) PL (Completed) RO (Completed) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-000637-39 | Sponsor Protocol Number: P7977-2025 | Start Date*: 2012-05-17 | ||||||||||||||||
| Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
| Full Title: An Open-Label Study to Explore the Clinical Efficacy of GS-7977 with Ribavirin Administered Pre-Transplant in Preventing Hepatitis C Virus (HCV) Recurrence Post-Transplant | ||||||||||||||||||
| Medical condition: Hepatitis C Virus (HCV) infection (all genotypes) in patients who have been placed on a wait list for liver transplantation from a deceased doner for hepatocellular carcinoma (HCC). | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-004760-39 | Sponsor Protocol Number: P05685 | Start Date*: 2009-04-03 | ||||||||||||||||||||||||||
| Sponsor Name:Schering Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
| Full Title: A phase 3 safety and efficacy study of boceprevir in combination with peginterferon alfa-2a and ribavirin in subjects with chronic hepatitis C genotype 1 who failed prior treatment with peginterfer... | ||||||||||||||||||||||||||||
| Medical condition: Chronic Hepatitis C | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) BE (Completed) IT (Completed) FR (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-001283-37 | Sponsor Protocol Number: GE-ARNICA-2008 | Start Date*: 2007-09-24 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: Chronic hepatitis C in illicit drug users and the role of antiviral therapy: the ARNICA project (Antiviral tReatment for chroNic hepatItis C in Active substance users) | |||||||||||||
| Medical condition: Chronic Hepatitis C | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021715-17 | Sponsor Protocol Number: 1220.7 | Start Date*: 2011-07-12 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
| Full Title: A phase III, randomised, double-blind and placebo controlled study of once daily BI 201335, 240 mg for 12 or 24 weeks in combination with pegylated interferon-α and ribavirin in patients with genot... | |||||||||||||
| Medical condition: Chronic hepatitis C infection genotype 1 | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) PT (Completed) BE (Completed) DE (Completed) AT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003114-12 | Sponsor Protocol Number: HBIG | Start Date*: 2022-11-04 | ||||||||||||||||
| Sponsor Name:Medical University of Graz | ||||||||||||||||||
| Full Title: Impact of Hepatitis B immunoglobulins in patients with chronic Hepatitis B on Hepatocellular Carcinoma – a proof of concept study | ||||||||||||||||||
| Medical condition: Patients with both chronic hepatitis B and hepatocellular carcinoma. | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-006131-38 | Sponsor Protocol Number: CDEB025A2312 | Start Date*: 2012-05-18 | |||||||||||
| Sponsor Name:Novartis Farmaceutica, S.A. | |||||||||||||
| Full Title: A multi-centre 3-year follow-up study to assess the durability of sustained virologic response in alisporivir treated chronic hepatitis C patients | |||||||||||||
| Medical condition: Chronic hepatitis C in patients who achieved sustained virologic response (SVR24) on alisporivir in a Novartis-sponsored chronic Hepatitis C study. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) HU (Completed) GB (Completed) PL (Completed) IT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002668-25 | Sponsor Protocol Number: VX11-950-115 | Start Date*: 2012-01-24 | |||||||||||
| Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
| Full Title: An Open-Label, Phase 3 Study of Telaprevir in Combination With Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Subjects Coinfected With Genotype 1 Hepatitis C Virus and Human Immunodef... | |||||||||||||
| Medical condition: chronic hepatitis C virus infection | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
| 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.