- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
28 result(s) found for: Aminotransferases.
Displaying page 1 of 2.
EudraCT Number: 2017-001762-13 | Sponsor Protocol Number: 747-401 | Start Date*: 2018-08-01 |
Sponsor Name:Intercept Pharmaceuticals, Inc. | ||
Full Title: A Phase 4, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Pharmacokinetics and Safety of Obeticholic Acid in Patients with Primary Biliary Cholangitis and Moderate to Severe Hepa... | ||
Medical condition: Primary Biliary Cholangitis and Moderate to Severe Hepatic Impairment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) DE (Prematurely Ended) BE (Completed) HU (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-001449-13 | Sponsor Protocol Number: XM02-04-INT | Start Date*: 2004-08-03 |
Sponsor Name:BioGeneriX AG | ||
Full Title: Safety and Efficacy of XM 02 in patients with Non-Hodgkin-Lymphoma receiving chemotherapy. | ||
Medical condition: Patients with Non-Hodgkin-Lymphoma receiving chemotherapy and developing Neutropenia due to chemotherapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001452-36 | Sponsor Protocol Number: XM02-02-INT | Start Date*: 2004-06-30 |
Sponsor Name:BioGeneriX | ||
Full Title: Efficacy and Safety of XM 02 compared to Filgrastim in patients with breast cancer receiving chemotherapy. Multinational, multicentre, randomised, controlled study | ||
Medical condition: Patients with breast cancer high risk stage II or stage III/IV (classification according to American Joint Committee on Cancer [AJCC] receiving chemotherapy and developing Neutropenia due to chemot... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003108-10 | Sponsor Protocol Number: GOING | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | |||||||||||||
Full Title: The GOING Study: Regorafenib followed by Nivolumab in patients with Hepatocellular Carcinoma progressing under sorafenib | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005660-86 | Sponsor Protocol Number: 06_DOG03_107 | Start Date*: 2006-07-19 |
Sponsor Name:Christie Hospital NHS Trust | ||
Full Title: A Phase II, open label, single arm study to evaluate Ticilimumab in Advanced Gastric/Oesophageal Adenocarcinoma | ||
Medical condition: Advanced Gastric/Oesophageal Adenocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003553-27 | Sponsor Protocol Number: WF10-05-001 | Start Date*: 2005-11-28 |
Sponsor Name:DIMETHAID AG | ||
Full Title: A SINGLE CENTRE, OPEN LABEL, PHASE II CLINICAL STUDY OF THE ADJUNCTIVE BENEFIT OF WF10 TO STANDARD CAPECITABINE CHEMOTHERAPY IN SUBJECTS WITH UNRESECTABLE PANCREATIC CANCER | ||
Medical condition: UNRESECTABLE PANCREATIC CANCER | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001564-37 | Sponsor Protocol Number: AGMT_HIV1 | Start Date*: 2013-12-02 | |||||||||||
Sponsor Name:Arbeitsgemeinschaft medikamentöse Tumortherapie gemeinnützige GmbH | |||||||||||||
Full Title: One arm, Open label, Interventional, non-comparative Study to assess Changes in Lipids and Lipoproteins in HIV infected Women with Hyperlipidemia after Switch from boosted Protease Inhibitors to Ra... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001200-20 | Sponsor Protocol Number: CSET 1287 | Start Date*: 2007-06-01 |
Sponsor Name:Institut Gustave Roussy | ||
Full Title: A Multicenter, Randomized Phase II Trial Assessing the Activity of Gemcitabine – Oxaliplatin Chemotherapy Alone or in Combination with Cetuximab in Patients with Advanced Biliary Cancer | ||
Medical condition: adenocarcinoma of the biliary tract ( gallbladder, intra and/ or extrahepatic bile ducts, ampulla of Vater) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017788-40 | Sponsor Protocol Number: KEO09069EST | Start Date*: 2010-10-20 | |||||||||||
Sponsor Name:CRLCC Alexis Vautrin | |||||||||||||
Full Title: Etude de phase II randomisée multicentrique évaluant l'efficacité d’estramustine phosphate (Estracyt ®) chez des patientes présentant un cancer du sein métastatique HER2- / RH+ ayant déjà reçu un t... | |||||||||||||
Medical condition: Metastases breast cancer in women already treated with aromatase inhibitors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001270-24 | Sponsor Protocol Number: A3671014 | Start Date*: 2007-02-13 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: Phase 2, single arm study of ticilimumab in patients with refractory metastatic adenocarcinoma of the colon or rectum | |||||||||||||
Medical condition: Refractory meatstatic adenocarcinoma of the colon or rectum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002826-70 | Sponsor Protocol Number: A3671008 | Start Date*: 2005-11-28 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, 10017, USA | |||||||||||||
Full Title: A Phase 2, open label, single arm study to evaluate the efficacy, safety, tolerability and pharmacokinetics of ticilimumab in patients with advanced refractory and/or relapsed melanoma | |||||||||||||
Medical condition: Malignant Melanoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004418-32 | Sponsor Protocol Number: U31402-A-U202 | Start Date*: 2020-10-30 | |||||||||||
Sponsor Name:DAIICHI SANKYO, INC | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL, PHASE 2 STUDY TO EVALUATE SAFETY AND EFFICACY OF U3-1402 IN SUBJECTS WITH ADVANCED OR METASTATIC COLORECTAL CANCER (CRC) | |||||||||||||
Medical condition: Advanced or metastatic colorectal cancer (CRC) which is resistant, refractory, or intolerant to at least 2 prior lines of therapy, that must include all of the following agents: fluoropyrimidine, i... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003692-35 | Sponsor Protocol Number: ZKSJ0109 | Start Date*: 2019-06-13 | |||||||||||
Sponsor Name:Friedrich Schiller University Jena | |||||||||||||
Full Title: Effects of empagliflozin on diuresis and renal function in patients with acute decompensated heart failure | |||||||||||||
Medical condition: acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002344-23 | Sponsor Protocol Number: 2020/490 | Start Date*: 2020-08-19 |
Sponsor Name:CHU de Besançon | ||
Full Title: Regorafenib in combination with metronomic cyclophosphamide, capecitabine, and low-dose aspirin in metastatic colorectal cancer carcinoma An open-label phase II | ||
Medical condition: Metastatic colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000741-46 | Sponsor Protocol Number: 2017/2523 | Start Date*: 2017-10-06 | |||||||||||
Sponsor Name:Gustave Roussy | |||||||||||||
Full Title: RANDOMIZED PHASE 2 TRIAL OF TWO CHEMOTHERAPY REGIMENS PLUS OR MINUS BEVACIZUMAB IN PATIENTS WITH WELL DIFFERENTIATED PANCREATIC NEUROENDOCRINE TUMORS | |||||||||||||
Medical condition: Pancreatic well differentiated neuroendocrine tumors (NET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004385-34 | Sponsor Protocol Number: ICM_2013/09 | Start Date*: 2014-05-27 | |||||||||||
Sponsor Name:Institut régional du Cancer - Montpellier - Val d'Aurelle | |||||||||||||
Full Title: Activity of Regorafenib in combination with modified Gemcitabine - Oxaliplatin Chemotherapy (mGEMOX) in patients with advanced Biliary Tract Cancer (BTC): A Phase Ib-II trial | |||||||||||||
Medical condition: advanced Biliary Tract Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001244-56 | Sponsor Protocol Number: LiCTOP-C-001 | Start Date*: 2013-07-23 | |||||||||||
Sponsor Name:Department of Pharmacy, Uppsala University | |||||||||||||
Full Title: An open, multicenter, single dose, parallel study, evaluating the pharmacokinetics of doxorubicin and its active metabolite (doxorubicinol) after a hepatic intra-arterial injection of either a lipi... | |||||||||||||
Medical condition: Intermediate hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002827-15 | Sponsor Protocol Number: A3671009 | Start Date*: 2006-01-19 | |||||||||||
Sponsor Name:Pfizer Ltd. [...] | |||||||||||||
Full Title: Phase 3, open label, randomized, comparative study of ticilimumab and either dacarbazine or temozolomide in patients with advanced melanoma | |||||||||||||
Medical condition: Advanced melanoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) AT (Completed) BE (Completed) SE (Completed) GR (Completed) CZ (Completed) SK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000906-20 | Sponsor Protocol Number: LUM001-601 | Start Date*: 2015-05-13 | ||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies Inc | ||||||||||||||||||
Full Title: An Open-label, Multicenter Extension Study to Evaluate the Long-term Safety of LUM001, an Apical Sodium-dependent Bile Acid Transporter Inhibitor (ASBTi), in Patients with Alagille Syndrome (ALGS) ... | ||||||||||||||||||
Medical condition: Alagille Syndrome (ALGS) and Progressive Familial Intrahepatic Cholestasis (PFIC) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015999-10 | Sponsor Protocol Number: XM22-03 | Start Date*: 2010-03-02 | |||||||||||||||||||||
Sponsor Name:BioGeneriX AG | |||||||||||||||||||||||
Full Title: Efficacy and Safety of XM22 compared to pegfilgrastim in patients with breast cancer receiving chemotherapy. A multinational, multicentre, randomised, double-blind controlled study | |||||||||||||||||||||||
Medical condition: Breast cancer high risk stage II, III or IV according to AJCC classification | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
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