- Trials with a EudraCT protocol (128)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
128 result(s) found for: Imatinib AND Glivec.
Displaying page 6 of 7.
EudraCT Number: 2005-001381-14 | Sponsor Protocol Number: CSTI5710109E2 | Start Date*: 2005-08-02 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II study to determine the safety and the anti- leukemic effects of STI571 in adults patients with Philadelphia chromosome positive leukemia including acute lymphoblastic le... | |||||||||||||
Medical condition: Philadelphia chromosome positive leukemia including acute lymphoblastic leukemia, acute myeloid leukemia and accelerate phase myeloid leukemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001380-61 | Sponsor Protocol Number: CSTI5710102E2 | Start Date*: 2005-04-15 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II open label study to determine the safety and anti-leukemic effects of STI571 in patients with Philadelphia chromosome positive chronic myeloid leukemia in myeloid blast c... | |||||||||||||
Medical condition: Ph+ CML in myeloid blast crisis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001382-33 | Sponsor Protocol Number: CSTI5710110E2 | Start Date*: 2005-04-15 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II study to determine the efficacy and the safety of STI571 in patients with chronic myeloid leukemia who are refractory to or intolerant of interferon-alpha | |||||||||||||
Medical condition: treatment of patients with CML who are refractory to or intolerant of interferon alpha. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005248-33 | Sponsor Protocol Number: CML1415 | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:Fondazione GIMEMA Franco Mandelli ONLUS | |||||||||||||
Full Title: SUSTRENIM Study – GIMEMA CML1415 Sustained treatment-free remission in BCR-ABL+ chronic myeloid leukemia: a prospective study comparing Nilotinib versus Imatinib with switch to Nilotinib in absence... | |||||||||||||
Medical condition: Chronic myeloid leukemia (CML) in chronic phase (CP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001298-42 | Sponsor Protocol Number: 1321 | Start Date*: 2016-01-19 | |||||||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||||||||||||
Full Title: A randomised phase II trial of imatinib alternating with regorafenib compared to imatinib alone for the first line treatment of advanced gastrointestinal stromal tumour (GIST) | |||||||||||||||||||||||
Medical condition: unresectable metastatic GIST | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Completed) ES (Completed) NO (Completed) FI (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) DK (Prematurely Ended) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004106-13 | Sponsor Protocol Number: NORDCML006 | Start Date*: 2009-03-23 | |||||||||||
Sponsor Name:University of Trondheim, NTNU, Norway | |||||||||||||
Full Title: An Open-Label, Randomized, Multicenter Phase II Trial Comparing the Depletion of Malignant Stem Cells with Dasatinib vs. Imatinib in Patients with Newly Diagnosed Chronic Phase Chronic Myeloid Leuk... | |||||||||||||
Medical condition: Chronic myeloid leukemia (CML) in chronic phase (CP) at diagnosis (untreated) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004722-82 | Sponsor Protocol Number: CSTI571E2204 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An exploratory study of the effects of Imatinib on allergic inflammation following out of allergy season repeated nasal allergen challenge in subjects with seasonal allergic rhinitis sensitive to T... | |||||||||||||
Medical condition: Seasonal Allergic Rhinitis (sensitivity to Timothy grass pollen) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-004165-20 | Sponsor Protocol Number: AITIK | Start Date*: 2023-04-26 | |||||||||||
Sponsor Name:CHU de Poitiers | |||||||||||||
Full Title: Discontinuation of Tyrosine Kinase Inhibitors in chronic myeloid leukemia and impact on the immune system: a randomized controlled trial of two therapeutic strategies | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006446-33 | Sponsor Protocol Number: CSTI571 basket 1 | Start Date*: 2007-03-20 | |||||||||||
Sponsor Name:ITALIAN SARCOMA GROUP | |||||||||||||
Full Title: Open-label trial of Imatinib in patients with Desmoid Tumor and Chondrosarcoma | |||||||||||||
Medical condition: Patients with Desmoid Tumor and Chondrosarcoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002280-24 | Sponsor Protocol Number: NILG-HES 1-03 | Start Date*: 2004-07-26 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: THERAPEUTIC AND BIOLOGICAL EFFECTS OF IMATINIB MESYLATE (STI571) IN PRIMARY HYPERESINOPHILIC SYNDROME (HES), CHRONIC EOSINOPHILIC LEUKEMIA (CEL) AND CHRONIC IDIOPHATIC HYPEREOSINOPHILIA (CIH): A ST... | |||||||||||||
Medical condition: HYPEREOSINOPHILIC SYNDROME (HES, CEL, CIH) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001508-19 | Sponsor Protocol Number: IMA-GVH | Start Date*: 2007-09-06 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. CARLO | |||||||||||||
Full Title: TRATTAMENTO CON IMATINIB MESILATO DELLA GVH CRONICA SEVERA SCLERODERMA-LIKE REFRATTARIA ALLA TERAPIA IMMUNOSOPRESSIVA CONVENZIONALE | |||||||||||||
Medical condition: GVH CRONICA ESTESA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001603-42 | Sponsor Protocol Number: AIL0115 | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:AIL CATANIA ASSOCIAZIONE ITALIANA CONTRO LEUCEMIE-LINFOMI E MIELOMA ONLUS | |||||||||||||
Full Title: “Arrest Imatinib or Dasatinib in CML patients with Deep Molecular Responses” (AID MORE) | |||||||||||||
Medical condition: Chronic phase CML patients with BCR-ABL/ABLIS transcript levels below MR3 (<0.1%) and above MR4.5 (>0.0032%) at the time of accrual. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020305-32 | Sponsor Protocol Number: CRAD001CIT27T | Start Date*: 2010-08-06 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: A phase II, open label study to evaluate the activity and safety of Everolimus in association to Imatinib in PDGFRA-D842V unresectable or metastatic gastrointestinal stromal tumours (GISTs)as... | |||||||||||||
Medical condition: patients with unresectable and/or metastatic gastrointestinal stromal tumours with exon 18 PDGFRA mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004669-17 | Sponsor Protocol Number: CSTI571E2205 | Start Date*: 2008-02-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, open-label, Proof of Concept (PoC) study to evaluate the efficacy and tolerability of STI571 for the treatment of fibrosis in patients with systemic sclerosis | |||||||||||||
Medical condition: Skin fibrosis in systemic sclerosis patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001790-41 | Sponsor Protocol Number: AB11002 | Start Date*: 2013-04-10 | |||||||||||
Sponsor Name:AB Science | |||||||||||||
Full Title: A prospective, multicenter, randomised, open-label, active-controlled, two-parallel groups, phase 3 study to compare the efficacy and safety of masitinib to sunitinib in patients with gastrointesti... | |||||||||||||
Medical condition: Gastrointestinal stromal tumor resistant to imatinib | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) ES (Ongoing) NL (Ongoing) DE (Prohibited by CA) BE (Prematurely Ended) AT (Ongoing) GB (GB - no longer in EU/EEA) GR (Prematurely Ended) IT (Suspended by CA) CY (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001779-39 | Sponsor Protocol Number: Be-Ce-Ima | Start Date*: 2006-03-20 | |||||||||||
Sponsor Name:Azienda Ospedaliera Universitaria S.Martino - U.O. Oncologia Medica - Genova | |||||||||||||
Full Title: Phase II trial FOLFOX combined with Bevacizumab, Cetuximab and Imatinib in patients with advanced untreated colorectal cancer | |||||||||||||
Medical condition: advanced untreated colorectal cancer in disease stage IV for which, second recent line-guide Poston JCO, October 2005 not is indication to the surgical treatment and that they have not been she d... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019189-94 | Sponsor Protocol Number: CLMAST01 | Start Date*: 2010-07-22 | ||||||||||||||||
Sponsor Name:Dr. Luis Escribano | ||||||||||||||||||
Full Title: Tratamiento con inhibidores de tirosina quinasas en pacientes con variantes de mastocitosis sistémica de mal pronóstico: ensayo clínico para sujetos sin mutación D816V de KIT y búsqueda de inhibido... | ||||||||||||||||||
Medical condition: Mastocitosis sistémica | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001477-82 | Sponsor Protocol Number: COGAALL0031 | Start Date*: 2012-03-16 | |||||||||||
Sponsor Name:Children's Oncology Group (COG) | |||||||||||||
Full Title: A Children’s Oncology Group pilot study for the treatment of very high risk acute lymphoblastic leukemia in children and adolescents | |||||||||||||
Medical condition: Acute lymphoblastic 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: (No results available) |
EudraCT Number: 2009-013271-22 | Sponsor Protocol Number: GIMEMA LAL1408 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL`ADULTO | |||||||||||||
Full Title: Front-line treatment of Ph positive (Ph+)/Bcr-Abl positive Acute Lymphoblastic Leukemia (ALL) with two tyrosine kinase inhibitors (TKI) (Imatinib and Nilotinib). A phase II exploratory multicentr... | |||||||||||||
Medical condition: Ph positive (Ph+)/Bcr-Abl positive 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: 2011-000440-22 | Sponsor Protocol Number: EURO-SKI01 | Start Date*: 2012-04-11 | |||||||||||
Sponsor Name:University of Heidelberg | |||||||||||||
Full Title: MULTICENTER TRIAL ESTIMATING THE PERSISTANCE OF MOLECULAR REMISSION IN CHRONIC MYELOID LEUKAEMIA AFTER STOPPING TKI | |||||||||||||
Medical condition: Patients with chronic myeloid leukemia with complete molecular response can stop tyrosine kinase inhibitors under close monitoring | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) FI (Completed) CZ (Completed) NL (Ongoing) NO (Completed) PT (Completed) AT (Prematurely Ended) ES (Ongoing) DK (Completed) | |||||||||||||
Trial results: (No results available) |
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