- 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 4 of 38.
EudraCT Number: 2016-003489-25 | Sponsor Protocol Number: GS-US-337-4063 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Multicenter, Open-Label Study to Evaluate the Efficacy and Safety of Ledipasvir/Sofosbuvir in Subjects with Genotype 1, 4, 5 and 6 Chronic HCV Infection Who are on Dialysis for End Stage... | ||||||||||||||||||
Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) IT (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: 2016-003625-42 | Sponsor Protocol Number: GS-US-342-4062 | Start Date*: 2017-03-24 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Multicenter, Open-Label Study to Evaluate the Efficacy and Safety of Sofosbuvir/Velpatasvir for 12 Weeks in Subjects with Chronic HCV Infection Who are on Dialysis for End Stage Renal Di... | ||||||||||||||||||
Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004335-29 | Sponsor Protocol Number: | Start Date*: 2007-05-30 | |||||||||||
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled factorial pilot study investigating Omacor and/or Fluvastatin in patients with chronic hepatitis C who have not responded to standard combination anti-viral therapy. | |||||||||||||
Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002010-37 | Sponsor Protocol Number: HBV1101 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Foundation for Liver research | |||||||||||||
Full Title: A Multi-center, Randomized, Open-label study for Induction of HBsAg decline using an add-on treatment of peginterferon alfa-2a in HBeAg-negative chronic hepatitis B patients treated with nucleos(t)... | |||||||||||||
Medical condition: Chronic hepatitis B virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002417-19 | Sponsor Protocol Number: GS-US-334-0126 | Start Date*: 2012-12-12 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc | ||||||||||||||||||
Full Title: A Phase 2, Multicenter, Open-Label Study to Investigate the Safety and Efficacy of GS-7977 and Ribavirin for 24 weeks in Subjects with Recurrent Chronic HCV Post Liver Transplant | ||||||||||||||||||
Medical condition: Recurrent Chronic HCV Post Liver Transplant | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001683-35 | Sponsor Protocol Number: GS-US-342-1138 | Start Date*: 2014-10-16 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks in Subjects with Chronic... | ||||||||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) IT (Completed) BE (Completed) FR (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: 2008-006453-40 | Sponsor Protocol Number: INFLTX08 | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:Karolinska University hospital Huddinge | |||||||||||||
Full Title: Peg-INF alfa-2a plus ribavirin treatment of liver transplant patients with hepatitis C relaps on protocol liver biopsies - a Nordic study on rapid viral response, early viral response, end of treat... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002283-32 | Sponsor Protocol Number: GS-US-334-1112 | Start Date*: 2014-10-15 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Open-Label, Multicenter, Multi-cohort, Single-Arm Study to Investigate the Safety and Efficacy of Sofosbuvir + Ribavirin in Adolescents and Children with Genotype 2 or 3 Chronic HCV Infe... | ||||||||||||||||||
Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) IT (Completed) GB (Completed) Outside EU/EEA BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004946-17 | Sponsor Protocol Number: TPL103922 | Start Date*: 2007-11-02 | |||||||||||
Sponsor Name:GlaxoSmithKline S.A. España | |||||||||||||
Full Title: Estudio multicéntrico aleatorizado, controlado con placebo, para evaluar la eficacia y la seguridad de eltrombopag en sujetos trombocitopénicos infectados por el virus de la hepatitis C (VHC) que, ... | |||||||||||||
Medical condition: Sujetos trombocitopénicos con infección vírica por Hepatitic C. Thrombocytopenic subjects with hepatitis C viral infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) BE (Completed) NL (Completed) IT (Completed) CZ (Completed) GB (Completed) SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004720-20 | Sponsor Protocol Number: VX07-950-108 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 3 Study of 2 Dose Regimens of Telaprevir in Combination With Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Treatment-Naive Subjects with Genotype 1 Chronic Hepatitis C | |||||||||||||
Medical condition: Chronic Hepatitis C, Genotype 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) FR (Completed) AT (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000292-42 | Sponsor Protocol Number: TPL108390 | Start Date*: 2007-12-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: ENABLE 2 (Eltrombopag to INitiate and Maintain Interferon Antiviral Treatment to Benefit Subjects with Hepatitis C related Liver DiseasE) Randomised, placebo-controlled, multi-centre study to asses... | |||||||||||||
Medical condition: Thrombocytopenic subjects with hepatitis C viral infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GR (Completed) BE (Completed) ES (Completed) IT (Completed) CZ (Completed) SK (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012344-17 | Sponsor Protocol Number: CICL670AIT06T | Start Date*: 2009-10-13 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: A randomized, open label, single center, phase IIa controlled trial to assess tolerability, safety and effect of treatment with deferasirox plus standard antiviral therapy versus standard antivira... | |||||||||||||
Medical condition: Chronic hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000824-12 | Sponsor Protocol Number: MK-5172-068 | Start Date*: 2014-06-06 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: A Phase III Randomized Clinical Trial to Study the Efficacy and Safety of the Combination Regimen of MK-5172/MK-8742 in Subjects who have Failed Prior Treatment with Pegylated Interferon and Ribavi... | |||||||||||||
Medical condition: Hepatitis C | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) ES (Completed) FI (Completed) PL (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005123-42 | Sponsor Protocol Number: VX06-950-107 | Start Date*: 2007-03-28 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Rollover Protocol of Telaprevir (VX-950) in Combination with Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Subjects Enrolled in the Control Group (Group A) of Study VX06-950-106 Wh... | |||||||||||||
Medical condition: Hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) GB (Completed) FR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001444-20 | Sponsor Protocol Number: CLDT600ACN03 | Start Date*: 2016-05-18 | |||||||||||
Sponsor Name:Beijing Novartis Pharma Co., Ltd. | |||||||||||||
Full Title: An Open-label, Single-arm, Multicenter, Phase IV, 52-week Study to Evaluate the Efficacy and Safety of Telbivudine 600mg Tablets in Chinese Patients with Chronic Hepatitis B | |||||||||||||
Medical condition: chronic hepatitis B | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000660-17 | Sponsor Protocol Number: TPL108392 | Start Date*: 2009-07-29 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: TPL108392: An open-label, multi-centre rollover study to assess the safety and efficacy of eltrombopag in thrombocytopenic subjects with hepatitis C virus (HCV) infection who are otherwise eligibl... | |||||||||||||
Medical condition: Thrombocytopenic subjects with hepatitis C viral infection (HCV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) GR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012459-96 | Sponsor Protocol Number: CIN-VHC-01 | Start Date*: 2010-06-08 | |||||||||||
Sponsor Name:Dr Calleja Panero | |||||||||||||
Full Title: VALORACIÓN INTENSIVA DE LA CINÉTICA DEL RNA DEL VIRUS DE LA HEPATITIS C COMO PREDICTOR PRECOZ DE AUSENCIA DE RESPUESTA VIROLÓGICA SOSTENIDA EN PACIENTES CON HEPATITIS CRÓNICA POR VHC TRATADOS CON I... | |||||||||||||
Medical condition: HEPATITIS C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022092-65 | Sponsor Protocol Number: ACH625-003 | Start Date*: 2011-10-13 | ||||||||||||||||
Sponsor Name:Achillion Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A phase IIa, randomized, double-blind (subject and investigator blind, sponsor open) placebo-controlled trial to evaluate the safety, tolerability and antiviral activity of oral ACH-0141625 in comb... | ||||||||||||||||||
Medical condition: Hepatitis C Virus Genotype 1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
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