- Trials with a EudraCT protocol (270)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
270 result(s) found for: Amylase.
Displaying page 7 of 14.
EudraCT Number: 2007-000527-18 | Sponsor Protocol Number: CSET 2006-1261 | Start Date*: 2007-04-13 |
Sponsor Name:Institut Gustave Roussy | ||
Full Title: Monocentric, open label, uncontrolled phase I-II study to evaluate the safety and the maximum tolerated dose of sorafenib given daily in combination with temozolomide (extended schedule) in patient... | ||
Medical condition: metastatic melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005367-10 | Sponsor Protocol Number: CRAF265A2101 | Start Date*: 2009-05-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase I/II, open-label, dose escalation trial to evaluate the safety, pharmacokinetics, and pharmacodynamics of RAF265 (CHIR-265) administered orally to patients with locally advanced or metastat... | |||||||||||||
Medical condition: local advanced or metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004384-19 | Sponsor Protocol Number: GIMEMA CML0408 | Start Date*: 2008-07-29 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Front-line treatment of Philadelphia positive (Ph pos), BCR-ABL positive, chronic myeloid leukemia (CML) with two tyrosine kinase inhibitors (TKI) (Nilotinib and Imatinib). A phase II exploratory m... | |||||||||||||
Medical condition: Philadelphia positive (Ph pos), BCR-ABL positive, Chronic Myeloid Leukemia (CML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001789-16 | Sponsor Protocol Number: PenCTU/2011/CTIMP-005 | Start Date*: 2011-08-26 | |||||||||||
Sponsor Name:Plymouth Hospital NHS Trust | |||||||||||||
Full Title: Investigation of the intra-tumoural concentration and activity of sorafenib in cutaneous schwannomas | |||||||||||||
Medical condition: Neurofibromatosis, type 2 (acoustic neurofibromatosis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003939-27 | Sponsor Protocol Number: 1-10-72-356-12 | Start Date*: 2013-02-12 | |||||||||||
Sponsor Name:Klaus Krogh | |||||||||||||
Full Title: Objective evaluation of the effects of pasireotide on gastrointestinal and colorectal transit times, rectal wall properties, and postprandial response in patients with carcinoid diarrhea | |||||||||||||
Medical condition: Patients with neuroendocrine tumors and carcinoid diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005177-21 | Sponsor Protocol Number: 2015-29 | Start Date*: 2016-01-28 |
Sponsor Name:Assistance Publique Hôpitaux de MARSEILLE | ||
Full Title: Dose-Finding of Propranolol in combination with metronomic fixed oral cyclophosphamide based on Bivariate efficacy-tolerability outcome in patients with locally advanced or metastatic angiosarcoma ... | ||
Medical condition: Patients presenting angiosarcomas disease | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005107-42 | Sponsor Protocol Number: GIMEMA LAL1205 | Start Date*: 2006-09-29 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL ADULTO | |||||||||||||
Full Title: A Phase II Multicenter Study on the Treatment of Adult de novo Philadelphia Chromosome Positive Ph Acute Lymphoblastic Leukemia ALL with the Protein Tyrosine Kinase Inhibitor BMS-354825. | |||||||||||||
Medical condition: Treatment of Adult de novo Philadelphia Chromosome Positive Ph Acute Lymphoblastic Leukemia ALL | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000758-30 | Sponsor Protocol Number: ONC-2006-004 | Start Date*: 2007-03-07 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Randomized continuation, dose escalation trial of Sorafenib in pts with advanced HCC with radiological progression on prior sorafenib treatment (Phase II study) | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004651-10 | Sponsor Protocol Number: Angio-Next-0710 | Start Date*: 2007-12-19 | |||||||||||
Sponsor Name:Centre Oscar Lambret | |||||||||||||
Full Title: Etude de phase II multicentrique stratifiée évaluant l’efficacité et la toxicité du Sorafenib dans le traitement des angiosarcomes localement avancés ou métastatiques non accessibles à une chirur... | |||||||||||||
Medical condition: ANGIOSARCOME LOCALEMENT AVANCE OU METASTATIQUE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007609-36 | Sponsor Protocol Number: SMAT - AN 20/04 | Start Date*: 2010-08-23 | ||||||||||||||||
Sponsor Name:University of Essen | ||||||||||||||||||
Full Title: Prospektiv randomisierte multizentrische Phase II-Studie zur Metastasenresektion von Lungenfiliae (poor-prognosis) beim klarzelligen Nierenzellkarzinom +/- adjuvante Sunitinibtherapie über 1 Jahr -... | ||||||||||||||||||
Medical condition: Kidney cancer with lung metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020798-17 | Sponsor Protocol Number: HGS1012-C1103 | Start Date*: 2011-07-01 | |||||||||||
Sponsor Name:Human Genome Sciences, Inc. (a wholly owned subsidiary of GlaxoSmithKline PLC) | |||||||||||||
Full Title: A Randomized, Multi-Center, Blinded, Placebo-Controlled Study of Mapatumumab ([HGS1012], a Fully Human Monoclonal Antibody to TRAIL-R1) in Combination with Sorafenib as a First-Line Therapy in Subj... | |||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004591-35 | Sponsor Protocol Number: ADVL1211 | Start Date*: 2018-12-14 |
Sponsor Name:National Cancer Institute Cancer Therapy Evaluation Program (NCI/CTEP) | ||
Full Title: A PHASE 1 STUDY OF XL184 (CABOZANTINIB, IND# 116059) IN CHILDREN AND ADOLESCENTS WITH RECURRENT OR REFRACTORY SOLID TUMORS, INCLUDING CNS TUMORS | ||
Medical condition: Patients with relapsed or refractory solid tumors including CNS tumors and malignant melanoma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-001295-37 | Sponsor Protocol Number: CILOGIST | Start Date*: 2018-10-10 |
Sponsor Name:CUB HOPITAL ERASME | ||
Full Title: CILOSTAZOL AS IMATINIB SYNERGISER IN PATIENTS WITH UNRESECTABLE OR METASTATIC GIST TREATED BY GLIVEC® | ||
Medical condition: Gastrointestinal stromal tumors. Gastrointestinal stromal tumors (GISTs) start their development in special cells in the wall of the gastrointestinal (GI) tract, also known as the digestive tract. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004644-24 | Sponsor Protocol Number: sorOVAR_07 | Start Date*: 2007-05-23 | |||||||||||
Sponsor Name:University of Bonn | |||||||||||||
Full Title: Prospective, open label, multi center phase II clinical trial with neoadjuvant chemotherapy in addition with Sorafenib in patients with primarily advanced ovarian cancer (FIGO IIIC + IV) and asci... | |||||||||||||
Medical condition: Ovarian Cancer; Stage FIGO IIIc and IV with more than 500 ml ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006393-29 | Sponsor Protocol Number: V00312 CA 201 | Start Date*: 2008-04-15 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT represented by Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: A 4-week double-blind placebo-controlled pilot study, evaluating niacin-induced flushing and lipid parameter effects of V0002 CA 1g 3 capsules/day associated with Niaspan® (from 375 mg to 1000 mg) ... | |||||||||||||
Medical condition: Dyslipidemia with uncontrolled elevated triglycerides | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022713-26 | Sponsor Protocol Number: CAMN107DDE12 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Localized gastrointestinal stromal tumors (GIST): an exploratory open-label, multicenter, single-arm phase II study to evaluate the efficacy of 2 years of adjuvant nilotinib treatment following at ... | |||||||||||||
Medical condition: localized gastrointestinal stromal tumors (GIST) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004637-16 | Sponsor Protocol Number: SLAP | Start Date*: 2009-04-28 | |||||||||||
Sponsor Name:GISCAD | |||||||||||||
Full Title: Folfiri as Second-Line chemotherapy for Advanced Pancreatic cancer: a GISCAD Phase II study | |||||||||||||
Medical condition: Subjects enrolled in this study must have histologically confirmed locally advanced or metastatic pancreatic adenocarcinoma. They must have been received a first-line chemotherapy (one line only) w... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000285-30 | Sponsor Protocol Number: TMC114IFD3001 | Start Date*: 2018-01-03 | |||||||||||
Sponsor Name:Janssen Research and Development | |||||||||||||
Full Title: Continued access to darunavir/ritonavir (DRV/rtv) in HIV-1 infected adults, adolescents and children aged 3 years and above. | |||||||||||||
Medical condition: Human Immunodeficiency Virus-1 infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001238-32 | Sponsor Protocol Number: ADVL1622 | Start Date*: 2019-09-26 |
Sponsor Name:National Cancer Institute Cancer Therapy Evaluation | ||
Full Title: Phase 2 Trial of XL184 (Cabozantinib) an Oral Small-Molecule Inhibitor of Multiple Kinases, in Children and Young Adults with Refractory Sarcomas, Wilms Tumor, and Other Rare Tumors | ||
Medical condition: Ewing sarcoma, Rhabdomyosarcoma, Non rhabdomyosarcoma, Wilms Tumor, Osteosarcoma and Other Rare Tumors | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-001901-18 | Sponsor Protocol Number: LGS.MMR.01.2016.2022 | Start Date*: 2017-02-14 | |||||||||||
Sponsor Name:The Danish National University Hospital "Rigshospitalet" | |||||||||||||
Full Title: Measles-mumps-rubella vaccine at 6 months of age, immunology, and childhood morbidity in a high-income setting | |||||||||||||
Medical condition: Infection with measles, mumps or rubella | |||||||||||||
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Population Age: Preterm newborn infants, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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