- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: FibroTest.
Displaying page 1 of 4.
| EudraCT Number: 2016-002442-23 | Sponsor Protocol Number: GS-US-428-4025 | Start Date*: 2017-01-09 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled Study Evaluating the Safety, Tolerability, and Efficacy of GS-9674 in Subjects with Primary Sclerosing Cholangitis Without Cirrhosis | |||||||||||||
| Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003370-33 | Sponsor Protocol Number: M15-684 | Start Date*: 2016-01-05 |
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
| Full Title: An Open-Label, Single Arm Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatment-Naïve Adults With Genotype 1b Hepatitis C Virus (HCV) Without Cir... | ||
| Medical condition: Hepatitis C Infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002443-42 | Sponsor Protocol Number: GS-US-427-4024 | Start Date*: 2017-01-09 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled Study Evaluating the Safety, Tolerability, and Efficacy of GS-9674 in Subjects with Primary Biliary Cholangitis Without Cirrhosis | |||||||||||||
| Medical condition: Primary Biliary Cholangitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003978-27 | Sponsor Protocol Number: GS-US-337-1119 | Start Date*: 2014-02-20 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Sofosbuvir/Ledipasvir Fixed-Dose Combination in Treatment-Naïve and Treatment-Experienced Subjects with Chronic Ge... | |||||||||||||
| Medical condition: Chronic Genotype 4 and Genotype 5 Hepatitis C Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013690-18 | Sponsor Protocol Number: GS-US-196-0112 | Start Date*: 2010-02-10 | |||||||||||
| Sponsor Name:Gilead Sciences Inc | |||||||||||||
| Full Title: A Phase 2, Randomized, Open-Label trial of GS-9256 plus GS-9190 alone and in combination with Ribavirin for 28 days in Treatment Naive Subjects with Chronic Genotype 1 Hepatitis C Virus Infection. | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) FR (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003187-37 | Sponsor Protocol Number: MK-5172-083 | Start Date*: 2016-01-25 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase II, Randomized, Open-Label Clinical Trial to Study the Efficacy and Safety of the Combination Regimen of Elbasvir/Grazoprevir (EBR/GZR) and Sofosbuvir (SOF) with and without Ribavirin (RBV)... | |||||||||||||
| Medical condition: Hepatitis C infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010912-14 | Sponsor Protocol Number: mi2-maicol-08 | Start Date*: 2009-04-06 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
| Full Title: MAraviroc In HIV/ HCV Coinfection and Liver fibrosis | ||||||||||||||||||
| Medical condition: HIV/ HCV Coinfection | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-001363-37 | Sponsor Protocol Number: RBHP_2016_ABERGEL | Start Date*: 2016-11-18 |
| Sponsor Name:CHU de Clermont-Ferrand | ||
| Full Title: A Phase 3, Global, Multicenter, Open-Label Study to Investigate the Efficacy of Elbasvir/Grazoprevir Fixed-Dose Combination for 8 Weeks in Treatment-Naïve, HCV GT1b-Infected Patients, with non-seve... | ||
| Medical condition: viral hepatitis C | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002496-10 | Sponsor Protocol Number: GS-US-402-1852 | Start Date*: 2017-02-21 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety, Tolerability, and Efficacy of GS-9674 in Subjects with Nonalcoholic Steatohepatitis (NASH) | |||||||||||||
| Medical condition: Nonalcoholic steatohepatitis (NASH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003898-42 | Sponsor Protocol Number: GS-US-342-1446 | Start Date*: 2015-01-26 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: An Open Label Study of Sofosbuvir/GS-5816 Fixed-Dose Combination in Subjects with Chronic HCV Infection | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-018523-26 | Sponsor Protocol Number: AOBSMI2ENT001-010 | Start Date*: 2010-03-17 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: Immediate versus delayed treatment with Entecavir in patients with active chronic hepatitis B (CHB): impact on liver fibrosis. | |||||||||||||
| Medical condition: Patients with chronic HBV infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2023-000160-54 | Sponsor Protocol Number: AT-01B-004 | Start Date*: 2023-05-17 |
| Sponsor Name:Atea Pharmaceuticals, Inc. | ||
| Full Title: PHASE 2, OPEN-LABEL STUDY TO ASSESS THE SAFETY AND EFFICACY OF BEMNIFOSBUVIR (BEM) AND RUZASVIR (RZR) IN SUBJECTS WITH CHRONIC HEPATITIS C VIRUS (HCV) INFECTION | ||
| Medical condition: Chronic Hepatitis C Virus (HCV) infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: RO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| 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: 2014-003304-73 | Sponsor Protocol Number: MK-3682-011 | Start Date*: 2015-01-21 |
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
| Full Title: A Phase II, Randomized, Open-Label Clinical Trial to Study the Efficacy and Safety of the Combination Regimen of MK-5172 and MK-3682 with Either MK-8742 or MK-8408 in Subjects with Chronic HCV GT1 ... | ||
| Medical condition: Chronic Hepatitis C infected patient | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) ES (Completed) DE (Completed) DK (Completed) LT (Completed) AT (Completed) PL (Completed) GB (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000137-22 | Sponsor Protocol Number: MK-5172-060 | Start Date*: 2014-06-30 |
| 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 Treatment-Naïve Subjects with Chronic HCV GT1, GT4, GT5, and GT6 Infection | ||
| Medical condition: Hepatitis C | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) SE (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001682-27 | Sponsor Protocol Number: GS-US-342-1140 | Start Date*: 2014-08-19 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks with Sofosbuvir and Ribavirin for 24 Weeks in Subje... | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C Virus Infection | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IT (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-015403-95 | Sponsor Protocol Number: NS10364-3 | Start Date*: 2010-02-11 |
| Sponsor Name:Faculty Hospital Hradec Králové | ||
| Full Title: A pilot trial of noninvasive assessment of methotrexate hepatotoxicity in the course of pharmacokinetically guided pharmacotherapy of psoriasis with methotrexate and folic acid | ||
| Medical condition: moderate-severe and severe plaque psoriasis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002296-17 | Sponsor Protocol Number: GS-US-337-0121 | Start Date*: 2013-09-02 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Sofosbuvir/Ledipasvir Fixed-Dose Combination for 12 Weeks with Ribavirin or for ... | |||||||||||||
| Medical condition: Chronic Genotype 1 Hepatitis C Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000785-37 | Sponsor Protocol Number: GS-US-320-1092 | Start Date*: 2016-08-26 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind Evaluation of the Pharmacokinetics, Safety, and Antiviral Efficacy of Tenofovir Alafenamide (TAF) in Adolescents with Chronic Hepatitis B Virus Infection | |||||||||||||
| Medical condition: Chronic Hepatitis B | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA BE (Completed) IT (Prematurely Ended) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003585-27 | Sponsor Protocol Number: GNS561CLIQ0211 | Start Date*: 2018-01-11 | |||||||||||||||||||||||||||||||
| Sponsor Name:GENOSCIENCE PHARMA | |||||||||||||||||||||||||||||||||
| Full Title: Phase 1/2a study to evaluate the safety, activity, and pharmacokinetics of escalating doses of GNS561 in patients with primary or secondary liver cancer | |||||||||||||||||||||||||||||||||
| Medical condition: Hepatocellular carcinoma Intrahepatic cholangiocarcinoma Pancreatic adenocarcinoma with liver metastasis Colorectal cancer with liver metastasis | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
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