- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
19 result(s) found for: Vindesine.
Displaying page 1 of 1.
EudraCT Number: 2008-004278-41 | Sponsor Protocol Number: 01081 | Start Date*: 2010-04-19 |
Sponsor Name:Institut Jules Bordet | ||
Full Title: A phase II study of doxorubicin, cyclophosphamide and vindesine with valproic acid in patients with refractory or relapsing small cell lung cancer after platinum derivatives and etoposide. | ||
Medical condition: This is a prospective phase II study investigating well-known chemotherapeutic (doxorubicin, cyclophosphamide, vindesine) and antiepileptic (valproate) agents, in combination, for the treatment of... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004772-12 | Sponsor Protocol Number: NLGPCNSL | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:Nordic Lymphoma Group | |||||||||||||
Full Title: Immunochemotherapy in Primary Central Nervous System Lymphoma with Rituximab, HD-MTX, HD-Ara C, cyclophosphamide, ifosfamide, vincristine, vindesine, temozolomide and DepoCyte induction followed by... | |||||||||||||
Medical condition: Newly diagnosed Primary Central Nervous Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015105-39 | Sponsor Protocol Number: 2008_36 | Start Date*: 2010-01-14 |
Sponsor Name:Centre Hospitalier Universiatire de Lille | ||
Full Title: Etude de phase II évaluant une chimiothérapie combinant doxorubicine, cyclophosphamide, vindésine et acide valproïque dans les cancers bronchiques à petites cellules réfractaires ou récidivant aprè... | ||
Medical condition: les cancers bronchiques à petites cellules | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000793-30 | Sponsor Protocol Number: IntReALL-SR-2010 | Start Date*: 2013-10-25 | |||||||||||
Sponsor Name:Charité - University Hospital of Berlin | |||||||||||||
Full Title: International Study for Treatment of Standard Risk Childhood Relapsed ALL 2010 | |||||||||||||
Medical condition: Acute lymphoblastic leukemia (ALL) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) PT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) AT (Completed) IE (Completed) FI (Completed) DK (Completed) CZ (Completed) IT (Completed) NL (Completed) FR (Completed) PL (Completed) ES (Prematurely Ended) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000699-18 | Sponsor Protocol Number: 2007.462/5 | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Randomized phase II study of two associations of rituximab and chemotherapy, with a pet-driven strategy, in patients from 18 to 59 with DLBCL CD20+ lymphoma and 2 or 3 adverse prognostic factors of... | |||||||||||||
Medical condition: CD20+ diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001691-39 | Sponsor Protocol Number: UKM17_0023 | Start Date*: 2019-07-16 | |||||||||||
Sponsor Name:University Hospital Münster | |||||||||||||
Full Title: LBL 2018 - International cooperative treatment protocol for children and adolescents with lymphoblastic lymphoma | |||||||||||||
Medical condition: Lymphoblastic lymphoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) DE (Ongoing) DK (Trial now transitioned) IE (Completed) NO (Trial now transitioned) FI (Trial now transitioned) AT (Trial now transitioned) CZ (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) NL (Ongoing) SK (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001068-31 | Sponsor Protocol Number: 2019/2894 | Start Date*: 2019-09-24 | ||||||||||||||||
Sponsor Name:Gustave Roussy | ||||||||||||||||||
Full Title: High-Risk Neuroblastoma Study 2 of SIOP-Europa-Neuroblastoma (SIOPEN) Randomized, international and multicentric phase 3 study that evaluates and compares 2 treatment strategies in 3 therapeutic p... | ||||||||||||||||||
Medical condition: Very High Risk Neuroblastoma | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) SI (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) CZ (Trial now transitioned) NO (Trial now transitioned) BE (Trial now transitioned) SE (Ongoing) SK (Trial now transitioned) ES (Ongoing) DE (Ongoing) AT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001641-33 | Sponsor Protocol Number: PETAL-Studie | Start Date*: 2007-07-25 |
Sponsor Name:Universitätsklinikum Essen | ||
Full Title: Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (Positron emission tomography guided therapy of aggressive non-Hodgkin's lymphomas) | ||
Medical condition: Aggressive non-Hodgkin's lymphomas (first line therapy) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012950-19 | Sponsor Protocol Number: GMALL-B-ALL/NHL 2002, NILG 2009 | Start Date*: 2009-10-30 | |||||||||||
Sponsor Name:NILG (Northern Italy Leukemia Group) | |||||||||||||
Full Title: Multicentre study to optimize therapy of B-ALL and high grade non-Hodgkin Lymphoma in Adults | |||||||||||||
Medical condition: Burkitt`s Lymphoma Burkitt`s Leukemia | |||||||||||||
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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: 2017-004883-37 | Sponsor Protocol Number: NB2015LR | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Prospective multicenter clinical trial for risk estimation and treatment stratification in low and intermediate risk neuroblastoma patients (NB2015-LR) | |||||||||||||
Medical condition: Neuroblastoma, low or intermediate risk | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009938-33 | Sponsor Protocol Number: IEO S460/109 | Start Date*: 2009-05-26 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Temozolomide in the chemo-immuno-therapy of refractory acute leukaemia of adult patients: The TRIAC protocol | |||||||||||||
Medical condition: Refractory acute leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016075-30 | Sponsor Protocol Number: GIMEMA LAL1308 | Start Date*: 2010-07-09 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL`ADULTO | |||||||||||||
Full Title: Therapy of the Young Adult Acute Lymphoblastic Leukemia (ALL): treatment intensification of the pediatric protocol AIEOP LLA-2000 | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006154-97 | Sponsor Protocol Number: 148/2006/U/Sper | Start Date*: 2007-01-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: HEMOS ALL 0105 Intensification therapy of mature B-ALL, Burkitt and Burkitt like and other HIgh Grade Non-Hodgkinメs Lymphoma in Adults | |||||||||||||
Medical condition: B-ALL, Burkitt and Burkitt like and Non-Hodgkinメs Lymphoma in Adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001935-12 | Sponsor Protocol Number: AIEOP-BFM-ALL-2017 | Start Date*: 2018-07-02 |
Sponsor Name:Universitätsklinikum Schleswig-Holstein, Campus Kiel | ||
Full Title: AIEOP-BFM ALL 2017 - International collaborative treatment protocol for children and adolescents with acute lymphoblastic leukemia | ||
Medical condition: acute lymphoblastic leukemia in children and adolescents <18 years of age | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) SK (Trial now transitioned) CZ (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003253-21 | Sponsor Protocol Number: 2013-99 | Start Date*: 2018-05-30 | |||||||||||
Sponsor Name:Universitätsklinikum Münster | |||||||||||||
Full Title: B-NHL 2013 - Treatment protocol of the NHL-BFM and the NOPHO study groups for mature aggressive B-cell lymphoma and leukemia in children and adolescents | |||||||||||||
Medical condition: mature aggressive B-cell lymphoma and leukemia in children and adolescents | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) DE (Trial now transitioned) SE (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) AT (Trial now transitioned) NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000760-21 | Sponsor Protocol Number: GMALL-EVOLVE | Start Date*: 2023-03-28 | |||||||||||
Sponsor Name:Goethe-University | |||||||||||||
Full Title: A multicentre, randomized trial in adults with de novo Philadelphia-Chromosome positive acute lymphoblastic leukemia to assess the efficacy of ponatinib versus imatinib in combination with low-inte... | |||||||||||||
Medical condition: De novo Philadelphia-Chromosome positive acute lymphoblastic leukemia (Ph+ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005019-29 | Sponsor Protocol Number: Rux-cALL-Pol_2020 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Medical University of Lodz | ||||||||||||||||||
Full Title: Single-arm interventional study with ruxolitinib and AIOEP-BFM2017 chemotherapy in children with acute lymphoblastic leukemia and confirmed activation of JAK/STAT pathway. | ||||||||||||||||||
Medical condition: Acute Lymphoblastic Leukemia with confirmed activating of JAK/STAT pathway in children and adolescents <18 years of age | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004270-43 | Sponsor Protocol Number: AIEOP-BFMALL2009 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein, Campus Kiel | |||||||||||||
Full Title: International collaborative treatment protocol for children and adolescents with acute lymphoblastic leukemia | |||||||||||||
Medical condition: acute lymphoblastic leukemia in children and adolescents 1 to <18 years of age | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005017-41 | Sponsor Protocol Number: AIEOP-BFM_2017_POLAND | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:Medical University of Silesia | |||||||||||||
Full Title: AIEOP-BFM 2017 POLAND - Collaborative treatment protocol for children and adolescents with acute lymphoblastic leukemia. A randomized phase III study conducted in agreement with the AIEOP-BFM study... | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia in children and adolescents <18 years of age | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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