- Trials with a EudraCT protocol (157)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
157 result(s) found for: Protein kinase.
Displaying page 5 of 8.
EudraCT Number: 2013-001265-16 | Sponsor Protocol Number: COEB071X2103 | Start Date*: 2013-09-30 |
Sponsor Name:Novartis Farma S.p.A | ||
Full Title: An Open-Label, Single-arm, Phase Ib/II study of AEB071 (a Protein Kinase C Inhibitor) and Everolimus (mTOR inhibitor) in Patients with CD79-mutant or ABC subtype Diffuse Large B-Cell Lymphoma | ||
Medical condition: Diffuse Large B-cell Lymphoma (DLBCL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) FR (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-002661-35 | Sponsor Protocol Number: FERRICCABG01 | Start Date*: 2020-04-23 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: Effect of Iron Isomaltoside on Perioperative Myocardial Injury in Patients Undergoing Coronary Artery Bypass Graft ± Valve Surgery: The Ferric Iron in Coronary Artery Bypass Grafting (FERRIC-CABG) ... | ||||||||||||||||||
Medical condition: Coronary or heart valve disease needing cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
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: 2007-006185-15 | Sponsor Protocol Number: SPIRIT 2 | Start Date*: 2008-04-22 | |||||||||||
Sponsor Name:Newcastle-upon-Tyne Hospitals NHS Trust | |||||||||||||
Full Title: STI571 Prospective International RandomIsed Trial 2 - A phase III, prospective randomised comparison of imatinib (STI571, Glivec/Gleevec) 400mg daily versus dasatinib (Sprycel) 100mg daily in pati... | |||||||||||||
Medical condition: newly-diagnosed chronic-phase Chronic myeloid leukaemia (CML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016669-27 | Sponsor Protocol Number: P10- | Start Date*: 2010-04-14 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A phase II study to investigate the efficacy of RAD001 (Afinitor®, everolimus) in patients with irresectable recurrent or metastatic differentiated, undifferentiated (anaplastic) and medullary thyr... | ||
Medical condition: Patients with irresectable recurrent or metastatic differentiated, undifferentiated (anaplastic) and medullary thyroid carcinoma will be treated in a phase II study to investigate the efficacy of R... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002291-41 | Sponsor Protocol Number: CC-486-MEL-001 | Start Date*: 2014-01-19 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Randomized, Open Label, Multi-Center Phase 2 Study of nab-Paclitaxel versus Epigenetic Modifying Therapy of CC-486 with nab-Paclitaxel in Subjects with Chemotherapy Naïve Metastatic Melanoma | |||||||||||||
Medical condition: Chemotherapy naïve metastatic melanoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000322-19 | Sponsor Protocol Number: UX007-CL202 | Start Date*: 2016-06-06 |
Sponsor Name:Ultragenyx Pharmaceutial Inc. | ||
Full Title: An Open-label Long-Term Safety and Efficacy Extension Study in Subjects with Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Previously Enrolled in UX007 or Triheptanoin Studies | ||
Medical condition: Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2019-002888-10 | Sponsor Protocol Number: SYD985.003 | Start Date*: 2020-03-25 | |||||||||||
Sponsor Name:Byondis BV | |||||||||||||
Full Title: A single-arm phase II trial to evaluate the safety and efficacy of the antibody-drug conjugate SYD985 in patients with HER2-expressing recurrent, advanced or metastatic endometrial carcinoma who pr... | |||||||||||||
Medical condition: Recurrent, Advanced or Metastatic Endometrial Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003108-15 | Sponsor Protocol Number: UC-GIG-2003 | Start Date*: 2022-11-04 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A multicentric national phase II trial assessing TIslelizumab in monotherapy for patients with Hepatocellular Carcinoma Child-Pugh B and ALBI grade 1 or 2 liver function Score | |||||||||||||
Medical condition: Hepatocellular Carcinoma (HCC), Child-Pugh B, ALBI grade 1 or 2 liver function | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002962-37 | Sponsor Protocol Number: NA_00008675 | Start Date*: 2010-09-14 |
Sponsor Name:VU Medical Center Amsterdam | ||
Full Title: Phase I/II study of dalteparin, a low molecular weight heparin (LMWH), in combination with Sunitinib (SU11248), an oral, selective multitargeted tyrosine kinase inhibitor, as first line treatment, ... | ||
Medical condition: Patients with metastatic or inoperable renal cell cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003436-13 | Sponsor Protocol Number: 105RC101 | Start Date*: 2016-05-24 | |||||||||||
Sponsor Name:TRACON Pharmaceuticals, Inc. | |||||||||||||
Full Title: A RANDOMIZED PHASE 2 TRIAL OF AXITINIB AND TRC105 VERSUS AXITINIB ALONE (INCLUDING A LEAD-IN PHASE 1B DOSE-ESCALATION PORTION) IN PATIENTS WITH ADVANCED OR METASTATIC RENAL CELL CARCINOMA | |||||||||||||
Medical condition: ADVANCED OR METASTATIC RENAL CELL CARCINOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Prematurely Ended) PL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003697-70 | Sponsor Protocol Number: VIB4920.P2.S3 | Start Date*: 2020-02-21 | |||||||||||
Sponsor Name:Viela Bio, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Mechanistic Insight and Dosage Optimization Study of the Efficacy and Safety of VIB4920 in Patients with Rheumatoid Arthritis (RA) | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000364-15 | Sponsor Protocol Number: SUNRISE-CRC | Start Date*: 2019-09-11 |
Sponsor Name:VU University Medical Center, Department of Medical | ||
Full Title: A randomized phase II/III study of pulsatile high-dose sunitinib versus TAS-102 in patients with metastatic colorectal carcinoma (mCRC). | ||
Medical condition: Advanced colorectal tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000973-40 | Sponsor Protocol Number: AB04030 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:AB SCIENCE | |||||||||||||
Full Title: A prospective, multicenter, randomized, open-label, active-controlled, 2-parallel group, phase III study to compare efficacy and safety of masitinib at 7.5 mg/kg/day to imatinib at 400 or 600 mg in... | |||||||||||||
Medical condition: gastro-intestinal stromal tumour | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Prematurely Ended) DE (Prohibited by CA) AT (Completed) BE (Prematurely Ended) ES (Prematurely Ended) NL (Temporarily Halted) GB (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001069-28 | Sponsor Protocol Number: D5881C00004 | Start Date*: 2015-02-10 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Long-Term Outcomes Study to Assess STatin Residual Risk Reduction with EpaNova in HiGh Cardiovascular Risk PatienTs with Hypertriglyceridemia (STRENGTH) | |||||||||||||
Medical condition: Severe persistent Hypertriglyceridemia in High Cardiovascular Risk Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) EE (Completed) LT (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000185-22 | Sponsor Protocol Number: 20110265 | Start Date*: 2014-12-03 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 1b/2, Multicenter, Open-label Trial of Talimogene Laherparepvec in Combination With MK-3475 for Treatment of Previously Untreated, Unresected, Stage IIIB to IVM1c Melanoma | |||||||||||||
Medical condition: Previously Untreated, Unresected, Stage IIIB to IVM1c Melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Prematurely Ended) BE (Completed) DE (Prematurely Ended) AT (Prematurely Ended) GR (Completed) IT (Prematurely Ended) FI (Prematurely Ended) CZ (Completed) PT (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001495-38 | Sponsor Protocol Number: XYN-602 | Start Date*: 2019-02-05 | ||||||||||||||||
Sponsor Name:Xynomic Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Phase 3, Double-blind, Placebo-controlled Study of Pazopanib With or Without Abexinostat in Patients With Locally Advanced or Metastatic Renal Cell Carcinoma | ||||||||||||||||||
Medical condition: Locally Advanced or Metastatic Renal Cell Carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002147-28 | Sponsor Protocol Number: CT-P16_3.1 | Start Date*: 2018-12-10 | |||||||||||
Sponsor Name:CELLTRION, Inc. | |||||||||||||
Full Title: A Double-Blind, Randomized, Active-Controlled, Parallel-Group, Phase 3 Study to Compare Efficacy and Safety of CT-P16 and EU-Approved Avastin as First-Line Treatment for Metastatic or Recurrent Non... | |||||||||||||
Medical condition: Metastatic or Recurrent Non-Squamous Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) BG (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004097-32 | Sponsor Protocol Number: CA033 | Start Date*: 2009-07-30 | ||||||||||||||||
Sponsor Name:Abraxis BioScience, LLC, a wholly owned subsidiary of Celgene Corporation | ||||||||||||||||||
Full Title: An Open-Label, Multicenter, Phase III Trial of ABI-007 vs Dacarbazine in Previously Untreated Patients with Metastatic Malignant Melanoma | ||||||||||||||||||
Medical condition: Metastatic Malignant Melanoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) NL (Completed) FR (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005036-26 | Sponsor Protocol Number: FXT-05 | Start Date*: 2011-11-29 | ||||||||||||||||||||||||||
Sponsor Name:Funxional Therapeutics Ltd | ||||||||||||||||||||||||||||
Full Title: An Exploratory Phase IIa Study to Investigate the Biological Activity of Oral FX125L in Adult Patients with Chronic Inflammatory Disease | ||||||||||||||||||||||||||||
Medical condition: Asthma Chronic obstructive pulmonary disease Rheumatoid arthritis Psoriasis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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