- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
33 result(s) found for: Kinases.
Displaying page 1 of 2.
EudraCT Number: 2011-002387-24 | Sponsor Protocol Number: CHU-P2011-05 | Start Date*: 2013-07-02 |
Sponsor Name:CHU Angers | ||
Full Title: Dyva-AAGG: Dysfonction vasculaire micro et macro vasculaire induite par les traitements anti-angiogéniques : Identification de nouveaux marqueurs pronostics | ||
Medical condition: cancer : rein, digestifs, pancréas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004686-34 | Sponsor Protocol Number: Evaluation Statin Therapy | Start Date*: 2007-02-27 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: Evaluation of Statin Therapy- Safety, Effect and Toxicity Mechanisms. | |||||||||||||
Medical condition: Frequency of side effects in patients treated with HMG CoA reductase inhibitors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001684-34 | Sponsor Protocol Number: HUM05/086 | Start Date*: 2006-06-21 |
Sponsor Name:Knud Kragballe, Dermatological Department, Århus Sygehus (Hospital) | ||
Full Title: Adalimumab clinical trial in plaque psoriasis – effect on expression of TNF-a and MAP-kinases in psoriatic skin – ACTION An open-label trial investigating adalimumab (HUMIRA) 80 mg s.c. at week 0 ... | ||
Medical condition: Patients with psoriasis vulgaris (plaque psoriasis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003098-26 | Sponsor Protocol Number: 3144A1-201-WW | Start Date*: 2006-06-06 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | ||
Full Title: Phase 2 Study of HKI-272 in Subjects with Advanced Breast Cancer | ||
Medical condition: Breast cancer is the most frequently diagnosed malignancy and the second most common cause of cancer related deaths in women. HER2 is a member of the epidermal growth factor receptor (EGFR) family ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002834-35 | Sponsor Protocol Number: PARERE | Start Date*: 2020-09-24 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: Randomized phase II study of PAnitumumab REchallenge followed by REgorafenib versus the reverse sequence in RAS and BRAF WILD-TYPE chemorefractory metastatic colorectal cancer patients. | |||||||||||||
Medical condition: RAS and BRAF wild-type chemorefractory metastatic colorectal cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004520-10 | Sponsor Protocol Number: ACNS1021 | Start Date*: 2019-06-25 |
Sponsor Name:National Cancer Institute (NCI) | ||
Full Title: 2018-004520-10 | ||
Medical condition: Recurrent, Refractory or Progressive High Grade Glioma and Ependymoma Tumors | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-004017-17 | Sponsor Protocol Number: RR11/9965 | Start Date*: 2013-04-08 |
Sponsor Name:The University of Leeds | ||
Full Title: Prospective, Single-centre, Open-Label, Randomised, Pilot Study Assessing the changes in expression of JAK-STAT and Speed & Depth of Remission Induced by Tocilizumab & Methotrexate Combination and ... | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003902-14 | Sponsor Protocol Number: 16-118 | Start Date*: 2017-07-06 |
Sponsor Name:RWTH Aachen University, represented by the Clinical Trial Center (CTC-A) | ||
Full Title: Intravenous Fish Oil based Lipid Emulsion as Pharmaconutrient Strategy in High-Risk Cardiac Surgery Patients: a Phase II Dosing Study | ||
Medical condition: Given the recently meta-analyzed data from previous RCTs about fish oil , we hypothesize that the provision of intravenous (i.v.) FO (0.20 g/kg and 0.50 g/kg) to cardiac surgery patients may reduc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002655-14 | Sponsor Protocol Number: 29BRC18.0144 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:CHRU BREST | |||||||||||||
Full Title: BAriCitinib Healing Effect in earLy pOlymyalgia Rheumatica (BACHELOR study) | |||||||||||||
Medical condition: polymyalgia rheumatica | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004031-31 | Sponsor Protocol Number: RVH006 | Start Date*: 2011-11-15 | |||||||||||
Sponsor Name:RespiVert Ltd | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group study to evaluate the safety and tolerability of treatment with repeat doses of inhaled RV568 in patients with COPD. | |||||||||||||
Medical condition: chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001988-52 | Sponsor Protocol Number: 90101 | Start Date*: 2012-07-30 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:EORTC | ||||||||||||||||||||||||||||||||||||||
Full Title: Cross-tumoral Phase 2 clinical trial exploring Crizotinib (PF-02341066) in patients with advanced tumours induced by causal alterations of either ALK or MET. | ||||||||||||||||||||||||||||||||||||||
Medical condition: Locally advanced and/or metastatic malignant tumor (anaplastic large cell lymphoma, inflammatory myofibroblastic tumor, papillary renal cell carcinoma type 1, alveolar soft part sarcoma, clear cell... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) NL (Completed) FR (Completed) NO (Completed) SI (Prematurely Ended) IT (Completed) PL (Completed) DK (Prematurely Ended) SK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002555-10 | Sponsor Protocol Number: DS1062-A-U304 | Start Date*: 2022-07-21 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A Randomized, Open-label, Phase 3 Trial of Dato-DXd Plus Pembrolizumab vs Pembrolizumab Alone in Treatment-naïve Subjects with Advanced or Metastatic PD-L1 High (TPS ≥50%) Non-small Cell Lung Cance... | |||||||||||||
Medical condition: Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) GR (Trial now transitioned) PT (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004341-17 | Sponsor Protocol Number: PCYC-1123-CA | Start Date*: 2014-10-16 | |||||||||||
Sponsor Name:Pharmacyclics LLC | |||||||||||||
Full Title: A Multicenter Open-Label Phase 1b/2 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination with Lenalidomide and Rituximab in Subjects with Relapsed or Refractory Diffuse... | |||||||||||||
Medical condition: Relapsed or Refractory Diffuse Large B-Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016952-36 | Sponsor Protocol Number: CR0708-12 | Start Date*: 2010-11-08 | |||||||||||
Sponsor Name:Cancer Research UK | |||||||||||||
Full Title: A Cancer Research UK Phase I trial of AT9283 (a selective inhibitor of aurora kinases) given over 72 hrs every 21 days via intravenous infusion in children and adolescents aged 6 months to 18 years... | |||||||||||||
Medical condition: Relapsed and refractory acute leukaemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022945-52 | Sponsor Protocol Number: ADVL0516 | Start Date*: 2012-01-26 | ||||||||||||||||
Sponsor Name:Children’s Oncology Group | ||||||||||||||||||
Full Title: A Phase 1 Study of BMS-354825 (Dasatinib) in Children with Recurrent/Refractory Solid Tumors or Imatinib Resistant Ph+ Leukemia. | ||||||||||||||||||
Medical condition: Refractory solid tumors Ph+ leukemia | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005572-17 | Sponsor Protocol Number: 15775407 | Start Date*: 2016-02-22 | |||||||||||
Sponsor Name:CHU TOULOUSE | |||||||||||||
Full Title: Assessment in real life of the association and its determinants between adverse events, and plasma concentrations of two protein kinases inhibitors: Ibrutinib (IMBRUVICA®) and idelalisib (ZYDELIG®)... | |||||||||||||
Medical condition: Hematological malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003674-26 | Sponsor Protocol Number: MK0457-009 | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:MERCK SHARP DOHME | |||||||||||||
Full Title: A Phase I Dose Escalation of MK-0457 in Combination With Dasatinib in Patients With Refractory Chronic Myelogenous Leukemia and Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia. | |||||||||||||
Medical condition: Patients with Refractory Chronic Myelogenous Leukemia and Philadelphia Chromosome-Positive Acute Lymphoblastic. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001184-11 | Sponsor Protocol Number: VIAject-15J | Start Date*: 2008-04-22 | |||||||||||
Sponsor Name:Biodel Inc | |||||||||||||
Full Title: Effect of prandial treatment with insulin VIAjectTM compared to regular human insulin and insulin lispro on postprandial endothelial function and microvascular stress in type 2 diabetic patients | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005542-23 | Sponsor Protocol Number: CR0708-11 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:Cancer Research UK | |||||||||||||
Full Title: A CCLG/Cancer Research UK Phase I Trial of AT9283 (a selective inhibitor of Aurora kinases) given for 72 hours every 21 days via intravenous infusion in children and adolescents with relapsed and r... | |||||||||||||
Medical condition: Relapsed and refractory solid tumours in children and adolescents | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003047-19 | Sponsor Protocol Number: Sym004-09 | Start Date*: 2016-03-02 | |||||||||||
Sponsor Name:Symphogen A/S | |||||||||||||
Full Title: An Open label, Multi-Center Phase 1b/2a Trial Investigating Different Doses of Sym004 in Combination with FOLFIRI in Patients with Metastatic Colorectal Cancer Progressing after First-Line Therapy | |||||||||||||
Medical condition: Patients with locally advanced or metastatic CRC, wild type KRAS/NRAS (exon 2, 3, 4) will be enrolled. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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