- 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 10 of 38.
EudraCT Number: 2022-002194-28 | Sponsor Protocol Number: NL81713.078.22 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Phase I/II study to determine the safety, immunogenicity and efficacy of Therapeutic Hepatitis B Virus Synthetic Long Peptide Vaccination (HEB-PEP-Study) | |||||||||||||
Medical condition: HBeAg negative chronic HBV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005709-20 | Sponsor Protocol Number: TMC435350-TiDP16-C202 | Start Date*: 2009-02-10 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals | |||||||||||||
Full Title: An open-label trial in genotype 2, 3, 4, 5 and 6 hepatitis C-infected subjects to evaluate the antiviral activity, safety, tolerability and pharmacokinetics of TMC435350 following 7 days once daily... | |||||||||||||
Medical condition: Hepatitis C virus (HCV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000452-24 | Sponsor Protocol Number: M13-576 | Start Date*: 2017-03-27 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Follow-up Study to Assess Resistance and Durability of Response to AbbVie Direct-Acting Antiviral Agent (DAA) Therapy (ABT-493 and/or ABT-530) in Subjects Who Participated in Phase 2 or 3 Clinic... | |||||||||||||
Medical condition: Hepatitis C Virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (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: 2011-004695-11 | Sponsor Protocol Number: AI452-020 | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3 Blinded Randomized Study of Peginterferon Lambda-1a and Ribavirin Compared to Peginterferon Alfa-2a and Ribavirin, Each Administered with Telaprevir in Subjects with Genotype-1 Chronic He... | |||||||||||||
Medical condition: Chronic Hepatitis C Virus (HCV) Infection (Genotype-1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) CZ (Completed) GB (Completed) PL (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005762-38 | Sponsor Protocol Number: M13-393 | Start Date*: 2012-05-31 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Coadministration of ABT-450 with Ritonavir (ABT-450/r) and ABT-267 in Adults with Chronic Hepatitis C Virus Infection (PEARL-I) | |||||||||||||
Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005151-42 | Sponsor Protocol Number: P05101 | Start Date*: 2008-08-28 | ||||||||||||||||||||||||||
Sponsor Name:Schering Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
Full Title: A Phase 3 Safety and Efficacy Study of Boceprevir in Subjects With Chronic Hepatitis C Genotype 1 Who Failed Prior Treatment With Peginterferon/Ribavirin | ||||||||||||||||||||||||||||
Medical condition: Chronic Hepatitis C | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) ES (Completed) IT (Completed) BE (Completed) DE (Completed) GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001789-34 | Sponsor Protocol Number: OptiB2007 | Start Date*: 2007-10-05 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: A multicenter open label study to explore the efficacy and tolerability of Tenofovir DF (TDF) (300 mg) in chronic hepatitis B, HBeAg positive or negative, patients with suboptimal response to adefo... | |||||||||||||
Medical condition: Chronic Hepatitis B HBV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018079-15 | Sponsor Protocol Number: IDX-07A-001 | Start Date*: 2010-05-03 | |||||||||||
Sponsor Name:Idenix Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase I/IIa Study Assessing Single and Multiple Doses of HCV Protease Inhibitor IDX320 in Healthy and Genotype 1 HCV-Infected Subjects | |||||||||||||
Medical condition: Healthy Volunteers and Genotype 1 HCV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007456-96 | Sponsor Protocol Number: GS-US-227-0106 | Start Date*: 2009-07-29 | |||||||||||
Sponsor Name:Gilead Sciences, Inc | |||||||||||||
Full Title: A Phase 2b, Double blind, Randomized, Parallel Group, Placebo Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of GS 9450 in Adults with Chronic Hepatitis C Virus Infection | |||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (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: 2019-001139-30 | Sponsor Protocol Number: YP39364 | Start Date*: 2019-07-10 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: A SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY STUDY OF RO7049389 IN: (1) SINGLE- (WITH OR WITHOUT FOOD) AND MULTIPLE- (WITH MIDAZOLAM) ASCENDING DOSES IN HEALTHY VOLUNTEERS; (2) PATIENTS C... | |||||||||||||
Medical condition: Chronic Hepatitis B | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001011-39 | Sponsor Protocol Number: GS-US-330-1401 | Start Date*: 2015-03-26 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Open-Label Study to Evaluate the Safety and Efficacy of GS-4774 in combination with Tenofovir Disoproxil Fumarate (TDF) for the Treatment of Subjects with Chronic Hepatitis B... | |||||||||||||
Medical condition: Chronic Hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000599-87 | Sponsor Protocol Number: 011094 | Start Date*: 2016-06-01 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: Response guided therapy with daclatasvir, sofosbuvir and ribavirin for 12 or 24 weeks in patients with genotype 3 chronic hepatitis C virus: is longer therapy worthwhile? | |||||||||||||
Medical condition: Adult patients chronically infected with genotype 3 hepatitis C virus with cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004885-14 | Sponsor Protocol Number: AI452-017 | Start Date*: 2012-11-20 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Controlled Study Evaluating the Efficacy and Safety of Peginterferon Lambda-1a, with and without Daclatasvir, Compared to Peginterferon Alfa-2a, Each in Combina... | |||||||||||||
Medical condition: Chronic Hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) FI (Completed) NL (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004360-10 | Sponsor Protocol Number: ALN-HBV-001 | Start Date*: 2016-04-06 | |||||||||||
Sponsor Name:Alnylam Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 1/2, Randomized, Single-Blind, Placebo-Controlled, Single-Ascending and Multiple-Ascending Dose, Safety, Tolerability, Pharmacokinetics, and Antiviral Efficacy Study of Subcutaneously Admin... | |||||||||||||
Medical condition: Chronic Hepatitis B virus (HBV) Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000629-55 | Sponsor Protocol Number: MRG-TEN-2011-01 | Start Date*: 2011-06-09 | |||||||||||
Sponsor Name:Manuel Rodríguez García | |||||||||||||
Full Title: CLINICAL TRIAL WITH TENOFOVIR VERSUS LAMIVUDINE PLUS ADEFOVIR DIPIVOXIL IN LAMIVUDINE-RESISTANT CHRONIC HEPATITIS-B PATIENTS WITH UNDETECTABLE VIRAL LOAD | |||||||||||||
Medical condition: CHRONIC HEPATITIS B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004129-28 | Sponsor Protocol Number: NP27946 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche | |||||||||||||
Full Title: Study To Evaluate Safety, Tolerability, Pharmacokinetics and Antiviral Activity of Ritonavir-Boosted DANOPREVIR in Combination With Peginterferon Alfa-2a Plus Ribavirin in Treatment-naive Patients ... | |||||||||||||
Medical condition: Chronic Hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002911-27 | Sponsor Protocol Number: BOC-PR | Start Date*: 2011-09-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PARMA | |||||||||||||
Full Title: Effect of boceprevir therapy on HCV-specific T cell responses: perspectives of immune monitoring and immune therapy | |||||||||||||
Medical condition: Chronic active hepatitis C never treated previously with anti-viral terapie | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012782-63 | Sponsor Protocol Number: P06086 | Start Date*: 2010-01-08 | ||||||||||||||||||||||||||
Sponsor Name:Schering-Plough Research Institution, A Division of Schering Corporation | ||||||||||||||||||||||||||||
Full Title: Boceprevir and Peginterferon/Ribavirin for the Treatment of Chronic Hepatitis C in Treatment-Naive Subjects: A Comparison of Erythropoietin Versus Ribavirin Dose Reduction for the Management of Anemia | ||||||||||||||||||||||||||||
Medical condition: Chronic Hepatitis C | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) DE (Completed) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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