- 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 3 of 7.
EudraCT Number: 2005-003166-42 | Sponsor Protocol Number: CSTI571BDE55 | Start Date*: 2005-12-27 | |||||||||||
Sponsor Name:University of Leipzig | |||||||||||||
Full Title: Palliative Chemotherapy (2nd line) with Imatinib (GlivecTM) in Patients with Bile Duct Cancer. | |||||||||||||
Medical condition: Patients with histologically proven adenocarcinoma of the gallbladder/bile duct (not papillary cancer) in an advanced stage, who have not responded to a first line chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013295-48 | Sponsor Protocol Number: 22505 | Start Date*: 2009-09-04 | |||||||||||
Sponsor Name:Århus University Hospital, Department of Dermatology | |||||||||||||
Full Title: Treatment of patients with Nephrogenic Systemic Fibrosis(NSF) with Imatinib Mesylate(Glivec). An open label clinical trial among patients with moderate to severe NSF. | |||||||||||||
Medical condition: Nephrogenic Systemic Fibrosis (NSF) is a fibrosing disease strongly associated with Gadolinium Based Contrast Agents(GBCA). Hard dermal plaques appear on legs, arms and abdomen. The lesions involve... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006181-41 | Sponsor Protocol Number: CA180399 | Start Date*: 2013-01-03 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: An open label, randomized (2:1) Phase 2b study of Dasatinib vs. Imatinib in patients with Chronic Phase Chronic Myeloid Leukemia who have not achieved an optimal response to 3 months of therapy wi... | |||||||||||||
Medical condition: Chronic Phase Chronic Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) BE (Completed) IT (Completed) AT (Completed) PL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000898-39 | Sponsor Protocol Number: SSGXXII | Start Date*: 2014-12-19 |
Sponsor Name:Scandinavian Sarcoma Group | ||
Full Title: Three versus five years of adjuvant imatinib as treatment of patients with operable GIST with a high risk for recurrence: A randomised phase III study. | ||
Medical condition: gastrointestinal stromal tumor (GIST) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) DK (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000218-19 | Sponsor Protocol Number: CSTI571BDE59 | Start Date*: 2008-05-21 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A single stage phase II, multi-centre, open label study of Glivec in combination with pioglitazone, etoricoxib, dexamethasone and low-dose treosulfane for anti-inflammatory and angiostatic treatmen... | |||||||||||||
Medical condition: prostrate carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016922-15 | Sponsor Protocol Number: HSJD-IMANF1 | Start Date*: 2010-02-04 |
Sponsor Name:HOSPITAL SANT JOAN DE DÉU | ||
Full Title: ENSAYO PILOTO CON IMATINIB PARA PACIENTES CON NEUROFIBROMA PLEXIFORME ASOCIADO A LA NEUROFIBROMATOSIS TIPO I. PILOT STUDY WITH IMATINIB FOR PLEXIFORM NEUROFIBROMA IN NEUROFIBROMATOSIS TYPE I PATIENTS | ||
Medical condition: Tratamiento de los neurofibromas plexiformes de alto riesgo no abordables quirúrgicamente en pacientes con neurofibromatosis tipo I | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001805-34 | Sponsor Protocol Number: CSTI571I1203 | Start Date*: 2017-08-15 |
Sponsor Name:Novartis Pharma K.K | ||
Full Title: Phase II Study of Imatinib Mesylate for Philadelphia-Positive Acute Lymphocytic Leukemia | ||
Medical condition: Philadelphia Chromosome Positive Acute Lymphocytic Leukemia (Ph+ALL) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-001339-69 | Sponsor Protocol Number: CML-paed-II-Study | Start Date*: 2008-01-25 | |||||||||||
Sponsor Name:THE TECHNICAL UNIVERSITY OF DRESDEN | |||||||||||||
Full Title: Protocol for standardized diagnostic procedures, registration, and treatment recommendations in children and adolescents with Philadelphia chromosome-positive chronic myeloid leukemia (CML). A mult... | |||||||||||||
Medical condition: Newly diagnosed patients with BCR-ABL-positive CML | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002538-20 | Sponsor Protocol Number: EORTC 62027 | Start Date*: 2006-02-24 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase 2 study of Glivec (Imatinib) in locally advanced and/or metastatic soft tissue sarcomas expressing the t(17;22)(q22;q13) translocation resulting in a COL1A1/PDGF rearrangement i.e. DermatoFib... | |||||||||||||
Medical condition: Soft tissue sarcomas are a family of malignant diseases originating from mesenchymal cells. Two types of theses sarcomas, dermatofibrosarcoma protuberans (DFSP) and giant cell fibriblastoma(GCF), a... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003883-20 | Sponsor Protocol Number: CSTI571JDE74 | Start Date*: 2008-09-30 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multicenter, expanded access study of imatinib mesylate in adult patients with GIST in adjuvant setting after R0-resection | |||||||||||||
Medical condition: gastrointestinal stromal tumors - adjuvant treatment after surgical tumor resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Completed) SK (Completed) CZ (Completed) BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006457-27 | Sponsor Protocol Number: CHUBX 2006/05 | Start Date*: 2007-02-27 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Essai clinique de phase II, comparatif, randomisé, en double insu, de l’imatinib mésylate STI571 (Glivec®) versus placebo chez des malades atteints de sclérodermie cutanée grave et de sclérodermie ... | ||
Medical condition: sclérodermie cutanée grave et de sclérodermie systémique avec atteinte cutanée grave | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2009-012616-40 | Sponsor Protocol Number: CAMN107A2405 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An Open Label, Randomized Study of Nilotinib vs. Standard Imatinib (400/600 mg QD) Comparing the Kinetics of Complete Molecular Response for CML-CP Patients with Evidence of Persistent Leukemia by ... | |||||||||||||
Medical condition: Chronic Myelogenous Leukemia in Chronic Phase | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005569-12 | Sponsor Protocol Number: CSTI571E2203 | Start Date*: 2006-01-26 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of six months treatment with the tyrosine kinase inhibitor of STI571 for the treatment of pulmonary arterial... | ||
Medical condition: pulmonary arterial hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Prematurely Ended) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005102-42 | Sponsor Protocol Number: INTERIM 0407 | Start Date*: 2007-12-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Phase II explorative study of intermittent Imatinib (IM) treatment (INTERIM) in elderly patients with Ph+ chronic myeloid leukemia (CML) who achieved a stable complete cytogenetic response (CCgR) w... | |||||||||||||
Medical condition: Patients with CML Ph+ CP that are in cytogentic response complete and stable for the last two years, treated with a Glivec daily dose | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000657-29 | Sponsor Protocol Number: CSTI571K2301 | Start Date*: 2005-07-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized open-label study of 400 mg versus 800 mg of Gleevec/Glivec (imatinib mesylate) in patients with newly diagnosed, previously untreated chronic myeloid leukemia in chronic phase (CML-CP)... | |||||||||||||
Medical condition: Newly diagnosed Philadelphia chromosome (bcr-abl) positive (Ph+) chronic myeloid leukemia in chronic phase (CML-CP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) ES (Completed) IT (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001547-43 | Sponsor Protocol Number: ET19-075 | Start Date*: 2022-01-18 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: ATEZOGIST – A prospective, randomized, multicenter, comparative study of the efficacy of imatinib resumption combined with atezolizumab versus imatinib resumption alone in patients with unresectabl... | |||||||||||||
Medical condition: Unresectable locally advanced or metastatic gastrointestinal stromal tumors (GIST) after failure of standard treatments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000770-36 | Sponsor Protocol Number: 2009-18 | Start Date*: 2013-05-14 |
Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007094-20 | Sponsor Protocol Number: IB 2009-07 | Start Date*: 2009-07-17 | |||||||||||
Sponsor Name:Institut Bergonié | |||||||||||||
Full Title: Étude multicentrique de phase III évaluant L’efficacité d’une stratégie d’adaptation de dose de l’imatinib mésylate sur la réponse moléculaire chez des patients présentant une leucémie myéloïde chr... | |||||||||||||
Medical condition: Patients présentant une leucémie myéloïde chronique en phase chronique (LMCPC) traités par IM depuis au moins 2 ans, en réponse cytogénétique complète depuis au moins 1 an, avec une maladie résidue... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005255-87 | Sponsor Protocol Number: 2014-13 | Start Date*: 2016-05-04 |
Sponsor Name:Assistance Publique Hôpitaux de MARSEILLE | ||
Full Title: Efficacy of adjuvant Imatinib in patients with intermediate-risk gastrointestinal stromal tumor with a high-risk Genomic Grade Index. Multicenter, prospective, randomized study. | ||
Medical condition: Patients with intermediate-risk gastrointestinal stromal tumor presenting a high Genomic Grade Index | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007988-16 | Sponsor Protocol Number: GICNO08.002 | Start Date*: 2009-05-08 |
Sponsor Name:OSPEDALE S. RAFFAELE | ||
Full Title: Imatinib piu` idrossiurea nel trattamento dei meningiomi recidivati o in progressione: studio randomizzato di fase II. | ||
Medical condition: patients affected by recurrent or progressive meningiomas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
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