- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
50 result(s) found for: Telaprevir.
Displaying page 1 of 3.
EudraCT Number: 2009-011464-11 | Sponsor Protocol Number: VX08-950-112 | Start Date*: 2009-10-20 | |||||||||||
Sponsor Name:Vertex Pharamceuticals, Inc. | |||||||||||||
Full Title: EXTEND: A 3-Year, Virology, Follow-up Study in Subjects Previously Treated With Telaprevir in Select Clinical Studies | |||||||||||||
Medical condition: Hepatitis C virus infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005636-26 | Sponsor Protocol Number: HCV12-01 | Start Date*: 2012-04-13 |
Sponsor Name:Foundation for Liver Research | ||
Full Title: Effect of Telaprevir in triple therapy for chronic hepatitis C patients on Intrahepatic immunological Mechanisms | ||
Medical condition: Chronic hepatitis C | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023669-23 | Sponsor Protocol Number: VX-950HEP3002 | Start Date*: 2011-04-06 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Multicenter, Open-Label, Early Access Program of Telaprevir in Combination With Peginterferon Alfa and Ribavirin in Genotype 1 Chronic Hepatitis C Subjects With Severe Fibrosis and Compensated Cirr... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IT (Completed) CZ (Completed) GR (Completed) ES (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000533-22 | Sponsor Protocol Number: VX-950-TiDP24-C216 | Start Date*: 2008-11-14 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, Phase III trial of 2 regimens of telaprevir (with and without delayed start) combined with pegylated interferon alfa-2a (Pegasys®) and ribavirin (Cop... | |||||||||||||
Medical condition: Chronic genotype 1 Hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) SE (Completed) FR (Completed) AT (Completed) IT (Completed) GB (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003729-27 | Sponsor Protocol Number: 0.8 | Start Date*: 2013-11-15 |
Sponsor Name:Queen Mary University of London | ||
Full Title: Telaprevir in patients with genotype 3 HCV : pilot clinical study to evaluate efficacy and predictability of therapy in patients who have failed to respond to pegylated interferon and ribavirin | ||
Medical condition: Genotype 3 HCV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021156-26 | Sponsor Protocol Number: VX10-950-022 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 1, Randomized, Open-label, Single-Dose, Crossover, Relative Bioavailability, and Food-Effect Study of a Pediatric Chewable Tablet Formulation Relative to a 375-mg Core Tablet Formulation of... | |||||||||||||
Medical condition: chronic hepatitis c virus genotype 1 infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005372-34 | Sponsor Protocol Number: UMCN-AKF12.02 | Start Date*: 2013-06-26 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
Full Title: The role of paroxetine in patients taking telaprevir-based HCV therapy: lack of a drug-drug interaction? (ROLEX) | ||||||||||||||||||
Medical condition: chronic hepatitis C infection with depression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005281-12 | Sponsor Protocol Number: VX-950-TiDP24-C210 | Start Date*: 2007-12-11 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A Phase IIa randomized, partially blinded trial of telaprevir (VX-950) in treatment-naïve subjects with chronic genotype 4 hepatitis C infection | |||||||||||||
Medical condition: Hepatitis C infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001419-21 | Sponsor Protocol Number: TPVAHC2012 | Start Date*: 2013-08-15 |
Sponsor Name:Universitätsklinikum Bonn | ||
Full Title: An open label, randomised, non-inferiority trial of pegylated interferon, ribavirin and telaprevir versus pegylated interferon and ribavirin alone in the response guided treatment of acute hepatiti... | ||
Medical condition: Acute Hepatitis C in HIV co-infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021628-84 | Sponsor Protocol Number: VX-950-C211 | Start Date*: 2011-03-29 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A randomized, open-label, Phase 3 study of telaprevir administered twice daily or every 8 hours in combination with pegylated interferon alfa-2a and ribavirin in treatment-naïve subjects with genot... | |||||||||||||
Medical condition: Hepatitis C Virus (HCV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) SE (Completed) AT (Completed) IE (Completed) PL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003593-85 | Sponsor Protocol Number: VX-950HPC3005 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Multicenter, Open-Label Study of Telaprevir in Combination With Peginterferon Alfa and Ribavirin in Human Immunodeficiency Virus/Genotype 1 Chronic Hepatitis C Coinfected Subjects With Severe Fibro... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) AT (Completed) DE (Completed) GB (Completed) PT (Completed) HU (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002920-14 | Sponsor Protocol Number: VX-950-TiDP24-C209 | Start Date*: 2007-11-14 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A Phase IIa randomized, partially blinded trial of telaprevir (VX-950) in treatment-naïve subjects with chronic genotype 2 or 3 hepatitis C infection | |||||||||||||
Medical condition: Hepatitis C infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) SE (Completed) IT (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: 2011-001323-21 | Sponsor Protocol Number: VX11-950-114 | Start Date*: 2012-01-31 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 3b Study of 2 Treatment Durations of Telaprevir, Peg-IFN (Pegasys®), and Ribavirin (Copegus®) in Treatment-Naive and Prior Relapser Subjects With Genotype 1 Chronic Hepatitis C and IL28B CC... | |||||||||||||
Medical condition: chronic hepatitis C virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) PL (Prematurely Ended) | |||||||||||||
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 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003754-84 | Sponsor Protocol Number: M13-774 | Start Date*: 2013-04-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Open-Label Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT-267 and ABT-333 Co-administered with and without Ribavirin Compared to Telaprevir Co-administered with Pe... | |||||||||||||
Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) FI (Completed) SK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002715-28 | Sponsor Protocol Number: NV27779 | Start Date*: 2011-12-09 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, DOUBLE-BLIND, MULTICENTER, PARALLEL GROUP STUDY TO EVALUATE THE SUSTAINED VIROLOGIC RESPONSE OF THE HCV POLYMERASE INHIBITOR PRODRUG RO5024048 IN COMBINATION WITH TELAPRE... | |||||||||||||
Medical condition: Chronic Hepatitis C (CHC), Genotype 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004564-30 | Sponsor Protocol Number: VX11-950-118 | Start Date*: 2013-02-12 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals | |||||||||||||
Full Title: A Two-Part, Open-Label, Single-Arm Phase 1/2 Study of Safety, Pharmacokinetics, and Efficacy of Telaprevir in Combination With Peginterferon alfa-2b and Ribavirin in Pediatric Subjects Aged 3 to 17... | |||||||||||||
Medical condition: genotype 1 Hepatitis C Virus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002515-25 | Sponsor Protocol Number: LLC-TEL-2012-1 | Start Date*: 2012-09-10 | ||||||||||||||||
Sponsor Name:Luis López Cortes - FISEVI | ||||||||||||||||||
Full Title: Pharmacokinetic interactions between Telaprevir and not powered Atazanavir with ritonavir in co-infected patients with HIV and HCV genotype 1 in treatment for chronic liver disease by HCV | ||||||||||||||||||
Medical condition: HIV–HCV co-infected patients | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004928-35 | Sponsor Protocol Number: VX-950HPC3008 | Start Date*: 2012-02-29 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Open-Label, Phase 3b Study to Determine Efficacy and Safety of Telaprevir, Pegylated-Interferon-alfa-2a and Ribavirin in Hepatitis C Virus Treatment-Naïve and Treatment-Experienced Subjects with Ge... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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