- Trials with a EudraCT protocol (28,311)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28,311 result(s) found for: A��������������������������� .c.
Displaying page 1 of 1,416.
EudraCT Number: 2011-000728-14 | Sponsor Protocol Number: ANA773-602 | Start Date*: 2011-05-10 | |||||||||||
Sponsor Name:Anadys Development, LTD | |||||||||||||
Full Title: A Phase 2a, Randomized, Open-Label Study in Patients with Chronic Hepatitis C Viral Infection to Assess the Safety, Tolerability, Pharmacodynamics, and Antiviral Activity of ANA773 Tosylate Adminis... | |||||||||||||
Medical condition: Chronic Hepatitis C Viral Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004185-17 | Sponsor Protocol Number: CDEB025A2222 | Start Date*: 2013-08-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, open-label, randomized, 3-arm, phase II profiling trial of pharmacokinetics, pharmacodynamics and safety of DEB025/Alisporivir in combination with ribavirin therapy in chronic hepa... | |||||||||||||
Medical condition: Chronic hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) GB (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001096-39 | Sponsor Protocol Number: MV25600 | Start Date*: 2012-07-10 | ||||||||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: An International, Multi-Center Study Evaluating the Correlation of IL28B Genotypes with Chronic Hepatitis C Disease Characteristics and Patient Demographics | ||||||||||||||||||
Medical condition: Chronic hepatitis C | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001942-16 | Sponsor Protocol Number: GS-US-334-0133 | Start Date*: 2012-08-10 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo Controlled Study to Investigate the Efficacy and Safety of GS-7977 + Ribavirin for 12 Weeks in Treatment-Naïve and Treatment-Experienced Su... | ||||||||||||||||||
Medical condition: Chronic Genotype 2 or 3 HCV Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) AT (Completed) NL (Completed) DE (Completed) GB (Completed) SE (Completed) ES (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001878-25 | Sponsor Protocol Number: IDX-08C-005 | Start Date*: 2011-11-17 | |||||||||||
Sponsor Name:Idenix Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind Study to Evaluate the Safety and Antiviral Activity of IDX184 in Combination with Pegylated Interferon and Ribavirin for 12 Weeks in Treatment-Naïve Subjects with Genotyp... | |||||||||||||
Medical condition: Genotype 1 Chronic Hepatitis C Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (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: 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: 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: 2004-004282-15 | Sponsor Protocol Number: C1 1304-01 | Start Date*: 2005-06-22 | |||||||||||
Sponsor Name:PHARMING TECHNOLOGIES B.V. | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind Phase III study of the efficacy and safety of recombinant human C1 inhibitor for the treatment of acute attacks in patients with hereditary angioedema | |||||||||||||
Medical condition: hereditary angioedema (HAE) treatment | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2007-002743-24 | Sponsor Protocol Number: STEPS in Geno Type 3 Cirrhotics | Start Date*: 2007-08-22 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: Study to evaluate different duration of treatment regimes of 40kD pegylated interferon alfa 2a (Pegasys) plus ribavirin on sustained virological responses (SVR) in Genotype 3 HCV infected cirrhotic... | |||||||||||||
Medical condition: Chronic hepatitis C infection with genotype 3 and advanced fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018361-33 | Sponsor Protocol Number: HCV689-201 | Start Date*: 2010-09-10 | ||||||||||||||||||||||||||
Sponsor Name:Arrow Therapeutics Ltd. (a member of the AstraZeneca group of companies) | ||||||||||||||||||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Determine the Efficacy, Safety and Tolerability of AZD7295 in Combination with Pegylated Interferon alpha-2a and Ribavirin in P... | ||||||||||||||||||||||||||||
Medical condition: Chronic hepatitis C virus (genotype 1b) infection | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SK (Completed) HU (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002348-14 | Sponsor Protocol Number: M15-464 | Start Date*: 2015-11-06 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults with Chronic Hepatitis C Virus Genotype 2 Infection (ENDURANCE-2) | |||||||||||||
Medical condition: Chronic HCV Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) PT (Completed) LT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005707-18 | Sponsor Protocol Number: SKS-0078 | Start Date*: 2008-08-07 | |||||||||||
Sponsor Name:Department of Infectious Diseases, Aarhus university Hospital, Skejby | |||||||||||||
Full Title: Clinical study of cerebral function in chronic hepatitis C virus patients treated with pegylated interferon alpha-2a and ribivirin | |||||||||||||
Medical condition: HCV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007075-16 | Sponsor Protocol Number: GE07-12 | Start Date*: 2008-12-01 | |||||||||||
Sponsor Name:VU university medical center | |||||||||||||
Full Title: The effect of peroxisome proliferator activator receptor γ agonist pre-treatment on pegylated interferon-α2a and ribavirin efficacy in hepatitis C patients, previously resistant to treatment with p... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2011-001071-40 | Sponsor Protocol Number: ISM10-06 | Start Date*: 2011-08-11 | ||||||||||||||||
Sponsor Name:InSpira Medical AB | ||||||||||||||||||
Full Title: A Phase IIa Safety study of oral administration of anti-CD3 monoclonal antibody in non-responder genotype-I chronic Hepatitis C subjects, a single-blind, randomized, controlled multi-center study | ||||||||||||||||||
Medical condition: in non-responder genotype-I chronic Hepatitis C subjects | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002483-26 | Sponsor Protocol Number: 1998/2005 | Start Date*: 2005-12-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Tailoring antiviral therapy of chronic hepatitis C to the single patient standard therapy versus treatment guided by a physic-mathematical model of the dynamics of Hepatitis C Virus infection. | |||||||||||||
Medical condition: Chronic Hepatitis C with or without cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000279-40 | Sponsor Protocol Number: SF3PEG-RIBA | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:A.S.L. 2 | |||||||||||||
Full Title: Randomised phase 3B study on comparison of 2 treatment schedules with peginterferon alpha 2b and ribavirin short term versus standard term schedules in patients with chronic hepatitis C, genotype... | |||||||||||||
Medical condition: Patients with chronic hepatitis C with genotype 2 or 3 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006588-21 | Sponsor Protocol Number: HLS02/2006 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Fluvastatin as adjuvant therapy to alfa-interferon and ribavirin in the treatment of chronic hepatitis C in patients with HIV-1 coinfection | |||||||||||||
Medical condition: Chronic hepatitis C in HIV/HCV coinfection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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