- Trials with a EudraCT protocol (5,507)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5,507 result(s) found for: Liver.
Displaying page 67 of 276.
| EudraCT Number: 2004-000558-22 | Sponsor Protocol Number: P02538 | Start Date*: 2005-06-20 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: Assessment of the safety, efficacy, tolerability and pharmacokinetics of PegIntron plus Rebetol in pediatric patients with chronic hepatitis C. | |||||||||||||
| Medical condition: Chronic Hepatitis C in pediatric patients. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) ES (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000344-25 | Sponsor Protocol Number: CDKO-125a-007 | Start Date*: 2013-04-22 |
| Sponsor Name:Nerviano Medical Sciences S.r.l. | ||
| Full Title: Phase II study of oral PHA-848125AC in patients with malignant thymoma previously treated with multiple lines of chemotherapy | ||
| Medical condition: Recurrent or metastatic, unresectable B3 thymoma or thymic carcinoma previously treated with multiple lines of chemotherapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004429-26 | Sponsor Protocol Number: Atu027-I-02 | Start Date*: 2013-02-25 | ||||||||||||||||
| Sponsor Name:Silence Therapeutics GmbH | ||||||||||||||||||
| Full Title: A Phase Ib/IIa study of combination therapy with Gemcitabine and Atu027 in subjects with locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
| Medical condition: Locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-001515-12 | Sponsor Protocol Number: 208127/120,/132,/133,/134,/137 | Start Date*: 2015-06-24 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase III, open, randomized, multicentre, multicountry study to compare the reactogenicity and evaluate the safety and immunogenicity of GSK Bio’s combined hepatitis A / hepatitis B vaccine (at l... | ||
| Medical condition: Vaccination of healthy children from 1 to 11 years old against Hepatitis | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005579-10 | Sponsor Protocol Number: A-93-52030-325 | Start Date*: 2016-02-26 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:IPSEN S.P.A. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: EFFICACY AND SAFETY OF LANREOTIDE ATG 120 MG IN COMBINATION WITH TEMOZOLOMIDE IN SUBJECTS WITH PROGRESSIVE WELL DIFFERENTIATED THORACIC NEUROENDOCRINE TUMORS | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: progressive well differentiated thoracic neuroendocrine tumors | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-002543-92 | Sponsor Protocol Number: PO3523 | Start Date*: 2007-01-31 | |||||||||||
| Sponsor Name:Schering-Plough Research Institute | |||||||||||||
| Full Title: A Safety and Efficacy Study of SCH 503034 in Previously Untreated Subjects With Chronic Hepatitis C Infected With Genotype 1 | |||||||||||||
| Medical condition: Chronic Hepatitis C | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) IT (Completed) NL (Completed) PT (Prematurely Ended) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005646-39 | Sponsor Protocol Number: BRTA-0100-016 | Start Date*: 2006-01-12 | |||||||||||
| Sponsor Name:NERVIANO MEDICAL SCIENCES | |||||||||||||
| Full Title: Phase II exploratory study of brostallicin PNU-166196A in patients with ovarian cancer resistant/refractory to platinum based chemotherapy. | |||||||||||||
| Medical condition: Advanced/metastatic ovarian cancer resistant or refractory to platinum. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002924-16 | Sponsor Protocol Number: FG-506-01-IT-02 | Start Date*: 2004-10-22 | |||||||||||
| Sponsor Name:FUJISAWA | |||||||||||||
| Full Title: AN OPEN, MULTICENTRE, RANDOMISED PARALLEL GROUP CLINICAL STUDY TO COMPARE SAFETY AND EFFICACY OF TACROLIMUS FK506 WITH MONOCLONAL ANTI-IL2R ANTIBODIES DACLIZUMAB VS TACROLIMUS FK506 WITH STER... | |||||||||||||
| Medical condition: PREVENTION OF REJECTION OF SUBOPTIMAL LIVERS IN LIVER ALLOGRAFT RECIPIENTS. COMPARE SAFETY AND EFFICACY OF TACROLIMUS FK506 WITH MONOCLONAL ANTI-IL2R ANTIBODIES DACLIZUMAB VS TACROLIMUS FK506 ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017716-32 | Sponsor Protocol Number: MEC09/02 | Start Date*: 2010-12-30 | |||||||||||
| Sponsor Name:Academic Medical Center | |||||||||||||
| Full Title: A phase II, randomized, placebo controlled study to evaluate the efficacy of the combination of gemcitabine, erlotinib and metformin in patients with locally advanced and metastastatic pancreatic c... | |||||||||||||
| Medical condition: locally advanced and metastatic pancreatic cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019505-42 | Sponsor Protocol Number: LEG-SIL-LTX-03 | Start Date*: 2010-05-26 |
| Sponsor Name:Rottapharm SpA | ||
| Full Title: ESTUDIO ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR LA EFICACIA Y SEGURIDAD DE LEGALON SIL EN EL TRATAMIENTO DE LA RECURRENCIA DE VHC EN EL INJERTO DE PACIENTES SOMETIDOS A UN T... | ||
| Medical condition: Pacientes de 18-70 años afectados por VHC en espera de de un trasplante ortotópico de hígado / 18-70 years old patients affected by HCV awaiting orthotopic liver transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005831-13 | Sponsor Protocol Number: CDKO-125a-005 | Start Date*: 2009-02-17 | |||||||||||
| Sponsor Name:NERVIANO MEDICAL SCIENCES | |||||||||||||
| Full Title: Phase II study of PHA-848125AC as second line-treatment in pemetrexed pre-treated malignant pleural mesothelioma patients | |||||||||||||
| Medical condition: Malignant Pleural Mesothelioma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006194-26 | Sponsor Protocol Number: EC11-185 | Start Date*: 2012-06-29 | |||||||||||
| Sponsor Name:JOSE LUIS MONTERO ALVAREZ | |||||||||||||
| Full Title: A phase IV, multicenter, randomized, double-blind, placebo-controlled study of efficacy and safety of Sorafenib in patients with hepatocellular carcinoma after radiological progression | |||||||||||||
| Medical condition: Advanced stage hepatocellular carcinoma (stage C of BCLC classification) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003306-45 | Sponsor Protocol Number: CBKM120ZDE01T | Start Date*: 2015-03-24 |
| Sponsor Name:Universitätsklinikum Tübingen | ||
| Full Title: An open-label, uncontrolled, single arm phase II trial of BKM120 (Buparlisib) in patients with metastatic melanoma with brain metastases not eligible for surgery or radiosurgery | ||
| Medical condition: metastatic melanoma with brain metastases | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2011-005675-16 | Sponsor Protocol Number: FBS0701-CTP-16 | Start Date*: 2012-05-15 |
| Sponsor Name:FERROKIN BIOSCIENCES INC. | ||
| Full Title: A Phase 2, 24 Week, Randomized, Open Label, Multi-Center Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two FBS0701 Doses in the Treatment of Chronic Iron Overlo... | ||
| Medical condition: Patients with transfusional iron overload, with the following primary diagnosis:hereditary anemia (such as sickle cell disease),β-thalassemia and Diamond Blackfan anemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-024068-16 | Sponsor Protocol Number: LAL-CL01 | Start Date*: 2011-03-08 | |||||||||||||||||||||
| Sponsor Name:Synageva Biopharma Corp. | |||||||||||||||||||||||
| Full Title: An open label multicenter study to evaluate the safety, tolerability and pharmacokinetics of SBC-102 in adult patients with liver dysfunction due to lysosomal acid lipase deficiency. | |||||||||||||||||||||||
| Medical condition: Lysosomal Acid Lipase (LAL) Deficiency is a rare autosomal recessive lipid storage disorder that is caused by deficient activity or absence, of the lysosomal enzyme, LAL. It is an extremely rare di... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-001531-20 | Sponsor Protocol Number: 103860/280,101695,101696,/697,/698 | Start Date*: 2015-06-26 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase III, single-blinded, randomized, multicentric study to compare the immunogenicity of GlaxoSmithKline Biologicals' thiomersal-free 2-dose Engerix™-B (20 mcg) and 3-dose preservative-free Eng... | ||
| Medical condition: Hepatitis B vaccination of healthy adolescents. | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003817-32 | Sponsor Protocol Number: LOLA-Merz:WMDHP39937 | Start Date*: 2013-01-08 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Brain muscle axis during treatment of hepatic encephalopathy with L-ornithine L-aspartate | |||||||||||||
| Medical condition: Hepatic Encephalopathy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019885-10 | Sponsor Protocol Number: Dermatux | Start Date*: 2011-01-05 | |||||||||||
| Sponsor Name:Universitätsmedizin Mainz (vertreten durch den wissenschaftlichen Vorstand) | |||||||||||||
| Full Title: Non-randomized phase-IV-study to investigate the efficacy of FOLFIRI in combination with cetuximab in the first-line treatment of metastatic colorectal cancer inculding a regular dermal prophylaxis... | |||||||||||||
| Medical condition: metastatic colorectal cancer (mCRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004370-14 | Sponsor Protocol Number: 20150930 | Start Date*: 2016-07-07 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: 89Zr-AMG211 PET imaging in patients with relapsed/refractory gastrointestinal adenocarcinoma before and during treatment with AMG 211 | ||
| Medical condition: Relapsed/refractory gastrointestinal adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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