- 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 13 of 38.
| EudraCT Number: 2006-000358-38 | Sponsor Protocol Number: P04755 | Start Date*: 2006-05-31 | |||||||||||
| Sponsor Name:Klinikum der J. W. Goethe-Universität Frankfurt - Medizinische Klinik I | |||||||||||||
| Full Title: Individually adapted therapy duration from 24 to 72 weeks for the treatment of patients with a chronic hepatitis C genotype 1 infection with Peginterferon alfa-2b plus Ribavirin in dependence of th... | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001049-10 | Sponsor Protocol Number: M14-726 | Start Date*: 2015-09-24 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: Open-label Study to Evaluate the Safety and Efficacy of the Combination of Ombitasvir, Paritaprevir/r ± Dasabuvir with Ribavirin (RBV) in Adult Patients with GT1 or GT4 Chronic HCV Infection and Re... | |||||||||||||
| Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004967-38 | Sponsor Protocol Number: M16-135 | Start Date*: 2017-08-01 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Single Arm, Open-label Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment Naïve Adults with Chronic Hepatitis C Virus (HCV) Genotype 1, 2, 4, 5 or 6 In... | |||||||||||||
| Medical condition: HCV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) PL (Completed) PT (Completed) HU (Completed) CZ (Completed) BG (Completed) IE (Completed) ES (Completed) GB (Completed) IT (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021925-12 | Sponsor Protocol Number: GS-EU-174-0160 | Start Date*: 2011-01-17 | |||||||||||
| Sponsor Name:Gilead Sciences International Ltd. | |||||||||||||
| Full Title: FINITE CHB - First investigation in stopping TDF treatment after long term virologic suppression in HBeAg-negative Chronic Hepatitis B | |||||||||||||
| Medical condition: Chronic Hepatitis B | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001464-36 | Sponsor Protocol Number: GS-US-174-0121 | Start Date*: 2008-12-12 | |||||||||||
| Sponsor Name:Gilead Science Incorporated | |||||||||||||
| Full Title: A Phase 3b, Randomized, Double-Blind, Double-Dummy Study Evaluating the Antiviral Efficacy, Safety, and Tolerability of Tenofovir Disoproxil Fumarate (DF) Monotherapy Versus Emtricitabine plus Teno... | |||||||||||||
| Medical condition: Chronic Hepatitis B | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) CZ (Completed) HU (Completed) ES (Completed) AT (Completed) GR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000905-30 | Sponsor Protocol Number: REM-TEN-2011-01 | Start Date*: 2011-07-08 | |||||||||||
| Sponsor Name:Rafael Esteban Mur | |||||||||||||
| Full Title: CLINICAL TRIAL WITH PROPHYLACTIC TENOFOVIR FOR HAEMATOLOGICAL CANCER PATIENTS SHOWING A HBc-Ab POSITIVE AND HBs-Ag PATTERN AND TO BE TREATED WITH RITUXIMAB (PREBLIN STUDY) | |||||||||||||
| Medical condition: CHRONIC HEPATITIS B | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005650-41 | Sponsor Protocol Number: ML19953 | Start Date*: 2006-05-11 | |||||||||||
| Sponsor Name:SESP | |||||||||||||
| Full Title: A Comparative, Randomized, Open-label, Multicenter Study, of Directly Observed Treatment of Chronic Hepatitis C (DOT) and auto administrated treatment with Copegus® (Ro 20-9963) and Pegasys® (Ro 25... | |||||||||||||
| Medical condition: Chronic Hepatitis C | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003535-27 | Sponsor Protocol Number: 1241.36 | Start Date*: 2012-10-17 | |||||||||||
| Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
| Full Title: A phase III randomised, partially double-blind and placebo-controlled study of BI 207127 in combination with faldaprevir and ribavirin for chronic genotype 1 hepatitis C infection in an extended p... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) GB (Completed) ES (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005500-14 | Sponsor Protocol Number: MZ-ATRACTION/ML 20804 | Start Date*: 2007-09-05 | |||||||||||
| Sponsor Name:Universitätsmedizin der Johannes-Gutenberg Universität Mainz | |||||||||||||
| Full Title: A Randomized, Open-label, Multicenter, Efficacy and Safety Study Examining the Effects on Viral Kinetics of All-trans Retinoic Acid (Tretinoin) (VESANOID®)in Combination with PEG-IFN alfa 2a (PEGA... | |||||||||||||
| Medical condition: chronic HCV infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012613-21 | Sponsor Protocol Number: VX-950-TiDP24-C219 | Start Date*: 2010-06-02 | |||||||||||
| Sponsor Name:Tibotec BVBA | |||||||||||||
| Full Title: An open-label, single-arm, roll-over trial of telaprevir in combination with pegylated interferon alfa-2a (Pegasys®) and ribavirin (Copegus®) for subjects from the control group of the VX-950-TiDP2... | |||||||||||||
| Medical condition: chronic genotype 1 hepatitis C infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) BE (Completed) DE (Completed) FR (Completed) SE (Completed) PL (Completed) ES (Completed) AT (Completed) GB (Completed) IT (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: 2011-003299-36 | Sponsor Protocol Number: MK5172-012 | Start Date*: 2011-11-09 | |||||||||||
| Sponsor Name:MERCK SHARP & DOHME CORP. | |||||||||||||
| Full Title: A Randomized, Partially Double-Blind, Active-Controlled, Dose-Ranging Estimation Study to Evaluate the Safety, Tolerability, and Efficacy of Different Regimens of MK-5172 When Administered Concom... | |||||||||||||
| Medical condition: HCV GT2/3 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002574-39 | Sponsor Protocol Number: 207811 | Start Date*: 2018-11-08 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: Ancillary study evaluating ChAd155-hIi-HBV shedding in a subset of chronic hepatitis B patients enrolled in the first-time-in-human, Phase I/II, randomised, multi-centric, single-blind study TH HBV... | |||||||||||||
| Medical condition: Chronic hepatitis B | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010149-29 | Sponsor Protocol Number: AI444-014 | Start Date*: 2009-05-07 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 2a Study of BMS-790052 in Combination with Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Treatment Naive Subjects with Chronic Hepatitis C Virus Genotype 1 Infection | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Genotype 1 Infection in Treatment Naïve Subjects | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006221-77 | Sponsor Protocol Number: CRO 768 | Start Date*: 2007-06-26 | |||||||||||||||||||||
| Sponsor Name:Clinical Research office, Faculty of Medicine, Imperial College London | |||||||||||||||||||||||
| Full Title: Warfarin Anticoagualtion for liver fibrosis in patients transplanted for hepatitis C virus infection. | |||||||||||||||||||||||
| Medical condition: Liver fibrosis in patients infected with hepatitis C virus after liver transplantation. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-002704-34 | Sponsor Protocol Number: HGS1008-C1067 | Start Date*: 2007-04-27 | |||||||||||
| Sponsor Name:Human Genome Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Multi-Center Study to Evaluate the Efficacy and Safety of Albumin Interferon Alfa-2b (alb-IFN) in Combination with Ribavirin Compared with Peginterferon Alfa-2a (PEGASYS or P... | |||||||||||||
| Medical condition: Chronic Hepatitis C (CHC) genotype 2/3. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FR (Completed) SE (Completed) GB (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002703-13 | Sponsor Protocol Number: HGS1008-C1060 | Start Date*: 2007-03-20 | |||||||||||
| Sponsor Name:Human Genome Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Multi-Center Study to Evaluate the Efficacy and Safety of Albumin Interferon Alfa-2b (alb-IFN) in Combination with Ribavirin Compared with Peginterferon Alfa-2a (PEGASYS or P... | |||||||||||||
| Medical condition: Chronic hepatitis C (CHC) genotype 1. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) AT (Completed) FR (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-015705-40 | Sponsor Protocol Number: AI463203 | Start Date*: 2010-04-08 | |||||||||||
| Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||
| Full Title: Protocol AI463203: A Study of the Safety and Efficacy of Entecavir plus Tenofovir in Adults with Chronic Hepatitis B Virus Infection with Previous Nucleoside/Nucleotide Treatment Failure | |||||||||||||
| Medical condition: Chronic Hepatitis B Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) IT (Completed) DE (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005409-65 | Sponsor Protocol Number: AI452-021 | Start Date*: 2013-01-18 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 3 Evaluation of Daclatasvir in Combination with Peginterferon Lambda-1a and Ribavirin (RBV) or Telaprevir in Combination with Peginterferon Alfa-2a and RBV in Patients with Chronic Hepatiti... | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection (Genotype 1b) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) IT (Completed) DE (Completed) PL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005431-23 | Sponsor Protocol Number: MNA-3521-014-RNDZ | Start Date*: 2022-03-31 | ||||||||||||||||||||||||||
| Sponsor Name:MiNA Alpha Limited | ||||||||||||||||||||||||||||
| Full Title: AN OPEN LABEL, RANDOMISED, PHASE 2 STUDY TO EVALUATE THE SAFETY AND EFFICACY OF MTL-CEBPA ADMINISTERED IN COMBINATION WITH SORAFENIB OR SORAFENIB ALONE, IN TKI NAÏVE PARTICIPANTS WITH PREVIOUSLY TR... | ||||||||||||||||||||||||||||
| Medical condition: Advanced hepatocellular cancer (HCC) as result of hepatitis B and/or hepatitis C | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: AT (Prematurely Ended) FR (Completed) BE (Prematurely Ended) SE (Prematurely Ended) NL (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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