- Trials with a EudraCT protocol (381)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
381 result(s) found for: Hepatitis D.
Displaying page 2 of 20.
EudraCT Number: 2012-003508-11 | Sponsor Protocol Number: AI452-033 | Start Date*: 2013-08-09 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Double-Blinded, Randomized Control Study Evaluating the Efficacy and Safety of Peginterferon Lambda-1a Compared to Peginterferon alfa-2a, Each in Combination with Ribavirin, in the Treatment of N... | |||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection (Genotype 1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001993-78 | Sponsor Protocol Number: VIR-CHDV-V201 | Start Date*: 2023-01-05 | ||||||||||||||||
Sponsor Name:Vir Biotechnology, Inc. | ||||||||||||||||||
Full Title: A Phase 2 Study to Evaluate Efficacy, Safety and Tolerability of VIR-2218 and VIR-3434 in Participants with Chronic Hepatitis D Virus Infection (SOLSTICE) | ||||||||||||||||||
Medical condition: Chronic Hepatitis D Virus (HDV) Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Trial now transitioned) NL (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001061-14 | Sponsor Protocol Number: CI-PSI-5268-06-305 | Start Date*: 2007-06-28 | |||||||||||
Sponsor Name:Pharmasset, Inc. | |||||||||||||
Full Title: A Multi-center, Randomized, Double-Blind, Active-Control, 96 Week, Phase III Trial of the Efficacy and Safety of Clevudine Compared with Adefovir at Weeks 48 and 96 in Nucleoside Treatment-Naïve Pa... | |||||||||||||
Medical condition: Chronic hepatitis due to hepatitis B virus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) ES (Completed) GB (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015002-19 | Sponsor Protocol Number: VTI-206 | Start Date*: 2010-01-18 | |||||||||||
Sponsor Name:VITAL THERAPIES INCORPORATED | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ELAD IN SUBJECTS WITH ACUTE ON CHRONIC HEPATITIS (AOCH) | |||||||||||||
Medical condition: Acute on Chronic Hepatitis (AOCH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001639-10 | Sponsor Protocol Number: 787-201 | Start Date*: 2023-06-09 | |||||||||||
Sponsor Name:Intercept Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Dose-escalation, Proof-of-Concept Study Evaluating the Safety, Tolerability, Efficacy and Pharmacokinetics of INT-787 in Subje... | |||||||||||||
Medical condition: Severe Alcohol-Associated Hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001063-30 | Sponsor Protocol Number: CI-PSI-5268-06-306 | Start Date*: 2007-06-28 | |||||||||||
Sponsor Name:Pharmasset, Inc. | |||||||||||||
Full Title: A Multi-center, Randomized, Double-Blind, Active-Control, 96 Week, Phase III Trial of the Efficacy and Safety of Clevudine Compared with Adefovir at Weeks 48 and 96 in Nucleoside Treatment-Naïve Pa... | |||||||||||||
Medical condition: Chronic hepatitis due to hepatitis B virus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) ES (Completed) GB (Prematurely Ended) GR (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: 2014-004751-31 | Sponsor Protocol Number: Heparc-2003 | Start Date*: 2015-06-26 | |||||||||||
Sponsor Name:Arrowhead Research Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Multi-dose Study to Determine the Depth of Hepatitis B Surface Antigen (HBsAg) Reduction Following Intravenous ARC-520 in Combination wi... | |||||||||||||
Medical condition: Chronic Hepatitis B Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019367-11 | Sponsor Protocol Number: ANRS HB 06 | Start Date*: 2010-08-30 | |||||||||||
Sponsor Name:ANRS | |||||||||||||
Full Title: ANRS HB 06 PEGAN Essai de phase III, randomisé, multicentrique, sans insu, évaluant à S96 la perte de l’Ag HBs suite à un traitement de 48 semaines par l’interféron pégylé alpha 2a chez des patient... | |||||||||||||
Medical condition: Cette étude va évaluer la perte de l’Ag HBs lors d’un traitement par l’interféron pégylé alpha-2a pendant 48 semaines chez des patients ayant une hépatite B chronique (AgHBe négatif), et une charge... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000080-25 | Sponsor Protocol Number: ML28262 | Start Date*: 2012-09-18 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A Phase IIb, Open Label, Single Arm, Multicenter Study to Evaluate the Effect of 48-weeks Peginterferon alfa-2a (PEG-IFN) Administration on Serum HBsAg in Chronic Hepatitis B, HBeAg-Negative, Genot... | |||||||||||||
Medical condition: Chronic Hepatitis B | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019584-10 | Sponsor Protocol Number: NV22776 | Start Date*: 2010-12-16 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche | |||||||||||||
Full Title: Estudio aleatorizado, abierto, multicéntrico, de búsqueda de dosis y duración del tratamiento para evaluar la respuesta virológica mantenida del inhibidor de proteasa VHC Danoprevir (RO5190591) ref... | |||||||||||||
Medical condition: Hepatitis C Crónica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) GB (Completed) AT (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2014-003894-41 | Sponsor Protocol Number: ImmunoPeg | Start Date*: 2014-11-21 | |||||||||||
Sponsor Name:Azienda Ospedaliero-Universitaria di Parma | |||||||||||||
Full Title: Effect of a Peg-interferon alfa 2A pulse on HBV-specific T cell responses in chronic hepatitis HBeAg negative patients under long-term nucleos(t)ide treatment | |||||||||||||
Medical condition: Chronic hepatitis B infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2014-004145-27 | Sponsor Protocol Number: Heparc-2002 | Start Date*: 2015-06-26 | |||||||||||
Sponsor Name:Arrowhead Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Multi-dose Study to Determine the Depth of Hepatitis B Surface Antigen (HBsAg) Reduction Following Intravenous ARC-520 in Combination wi... | |||||||||||||
Medical condition: Chronic Hepatitis B Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2005-001264-31 | Sponsor Protocol Number: P03659 | Start Date*: 2005-07-06 | |||||||||||
Sponsor Name:SCHERING-PLOUGH | |||||||||||||
Full Title: Peg-Intron/Rebetol vs Peg-Intron / SCH 503034 with and without Ribavirin in Chronic Hepatitis C HCV 1 Peginterferon alfa/Ribavirin Nonresponders: A SCH 503034 dose finding Phase 2 Study. | |||||||||||||
Medical condition: Adult patients with Chronic hepatitis C HCV-1 without cirrhosis nonresponders to a previous standard treatment of 12 weeks. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021967-34 | Sponsor Protocol Number: ANRS HC 25 VITAVIC | Start Date*: 2010-10-01 | |||||||||||
Sponsor Name:ANRS | |||||||||||||
Full Title: Essai clinique multicentrique, ouvert, prospectif évaluant l’efficacité d’une supplémentation par vitamine D en association à une bithérapie par interféron alpha pégylé plus ribavirine chez les pat... | |||||||||||||
Medical condition: Hépatite virale chronique C de génotype 1 ou 4 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
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: 2013-004043-23 | Sponsor Protocol Number: IDX-04B-001 | Start Date*: 2013-11-13 | |||||||||||
Sponsor Name:Idenix Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase I/IIa Study Assessing Single and Multiple Doses of IDX21437 in Healthy and HCV-Infected Subjects | |||||||||||||
Medical condition: Hepatitis C virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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