- Trials with a EudraCT protocol (664)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
664 result(s) found for: Leukaemias.
Displaying page 1 of 34.
| EudraCT Number: 2007-004480-21 | Sponsor Protocol Number: DSC/07/2357/28 | Start Date*: 2007-11-30 | |||||||||||
| Sponsor Name:ITALFARMACO | |||||||||||||
| Full Title: A phase IIA study of the histone-deacetylase inhibitor ITF2357 in patients with JAK-2 V617F positive chronic myeloproliferative diseases | |||||||||||||
| Medical condition: chronic myeloproliferative diseases | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001291-38 | Sponsor Protocol Number: 1230.27 | Start Date*: 2013-09-23 | ||||||||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co.KG | ||||||||||||||||||
| Full Title: Open, non-controlled, dose escalating Phase I trial to evaluate the pharmacokinetics, pharmacodynamics, tolerability and toxicity of volasertib in paediatric patients from 2 years to less than 18 y... | ||||||||||||||||||
| Medical condition: | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) IT (Completed) CZ (Completed) AT (Completed) SK (Completed) BE (Completed) NL (Completed) GB (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-003499-37 | Sponsor Protocol Number: DSC/11/2357/44 | Start Date*: 2013-01-20 | |||||||||||
| Sponsor Name:ITALFARMACO | |||||||||||||
| Full Title: Long-term study evaluating the effect of Givinostat in patients with JAK2V617F positive chronic myeloproliferative neoplasms. | |||||||||||||
| Medical condition: Chronic myeloproliferative neoplasms (cMPN). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) DE (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002171-13 | Sponsor Protocol Number: CC-5013-TCL-001 | Start Date*: 2007-11-22 | |||||||||||
| Sponsor Name:Celgene International Sàrl | |||||||||||||
| Full Title: A PHASE II, MULTICENTER, SINGLE-ARM, OPEN-LABEL STUDY TO EVALUATE THE SAFETY AND EFFICACY OF SINGLE-AGENT LENALIDOMIDE (REVLIMID®) IN SUBJECTS WITH RELAPSED OR REFRACTORY T-CELL NON-HODGKIN’S LYMPHOMA | |||||||||||||
| Medical condition: •Relapsed or refractory T-cell non Hodgkin's lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2008-006972-31 | Sponsor Protocol Number: Clo3o | Start Date*: 2008-11-27 | |||||||||||
| Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
| Full Title: Clinical phase II trial to evaluate the safety and efficacy of clofarabine and treosulfan conditioning prior to peripheral blood stem cells transplantation in paediatric and adult patients with adv... | |||||||||||||
| Medical condition: patients affected by advanced haematological malignancies | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005182-11 | Sponsor Protocol Number: ALLO-TREO | Start Date*: 2005-11-23 | |||||||||||
| Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
| Full Title: Clinical phase II trial to evaluate the safety and efficacy of treosulfan based conditioning prior to allogenic haematopoietic stem cell transplantation in patients with haematological malignancies. | |||||||||||||
| Medical condition: patients with haematologic maliignancies prior to allogenic haematopoietic stem cell | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018083-94 | Sponsor Protocol Number: IEO S513/110 | Start Date*: 2010-07-29 | ||||||||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | ||||||||||||||||||
| Full Title: Nonmyeloablative Hematopoietic Stem Cell Transplantation for Patients with High-Risk Hematologic Malignancies using Related, HLA-Haploidentical Donors: A Phase II Trial of Combined Immunosuppressio... | ||||||||||||||||||
| Medical condition: High risk Hematologic Malignancies | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2006-005195-40 | Sponsor Protocol Number: 61255762 | Start Date*: 2006-11-06 | |||||||||||
| Sponsor Name:Leila Niemi-Murola | |||||||||||||
| Full Title: Comparsion between articaine and lignocaine regional anaesthesian in patients undergoing bone marrow biopsy | |||||||||||||
| Medical condition: Patients suffering from different forms of leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020414-28 | Sponsor Protocol Number: AP24534-10-201 | Start Date*: 2011-02-21 | |||||||||||
| Sponsor Name:ARIAD Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Pivotal Phase 2 Trial of Ponatinib (AP24534) in Patients with Refractory Chronic Myeloid Leukemia and Ph+ Acute Lymphoblastic Leukemia | |||||||||||||
| Medical condition: Patients with Refractory Chronic Myeloid Leukemia and Ph+ Acute Lymphoblastic Leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) SE (Completed) DE (Completed) FR (Completed) BE (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001486-27 | Sponsor Protocol Number: 1301-LG | Start Date*: 2015-05-29 | |||||||||||||||||||||||||||||||
| Sponsor Name:European Orgainzation for the Research and Treatment of Cancer (EORTC) | |||||||||||||||||||||||||||||||||
| Full Title: 10-day decitabine versus conventional chemotherapy (“3+7”) followed by allografting in AML patients ≥ 60 years: a randomized phase III study of the EORTC Leukemia Group, CELG, GIMEMA and German MDS... | |||||||||||||||||||||||||||||||||
| Medical condition: Acute Myeloid Leukaemia (AML) in elderly population (equal or older than 60 years). | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) LT (Completed) SK (Completed) BG (Completed) NL (Completed) IT (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-006647-45 | Sponsor Protocol Number: D1060C00001 | Start Date*: 2009-05-14 | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: A Phase I/II, Open Label Multi-Centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the JAK2 inhibitor AZD1480 Administered Orally to Patients with Primary ... | ||||||||||||||||||
| Medical condition: Myeloproliferative disorders including Primary Myelofibrosis (PMF) and Post-Polycythaemia Vera/Essential Thrombocythaemia Myelofibrosis (Post-PV/ET MF). | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-004148-39 | Sponsor Protocol Number: TED15138 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
| Full Title: An open-label, first-in-human, dose escalation study of SAR440234 administered as single agent by intravenous infusion in patients with relapsed or refractory acute myeloid leukemia (R/R AML), B-ce... | |||||||||||||
| Medical condition: Leukaemia | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001416-30 | Sponsor Protocol Number: IDH2-Post-Allo-Trial | Start Date*: 2020-06-18 | |||||||||||
| Sponsor Name:Heinrich-Heine-University Düsseldorf represented by the Coordinating Investigator | |||||||||||||
| Full Title: IDH2-Post-Allo-Trial: Enasidenib as consolidation or salvage therapy for patients with IDH2 mutated AML or MDS following allogeneic blood stem cell transplantation | |||||||||||||
| Medical condition: Patients with myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML) or acute myelogenous leukemia (AML) after allogeneic stem cell transplantation (allo-SCT) and with an IDH2 mutat... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005537-11 | Sponsor Protocol Number: NCT-2007-11-02-1004 | Start Date*: 2011-07-12 | ||||||||||||||||
| Sponsor Name:University Hospital Heidelberg | ||||||||||||||||||
| Full Title: Phase I/II intra-patient dose escalation study of vorinostat in children with relapsed solid tumor, lymphoma or leukemia | ||||||||||||||||||
| Medical condition: Relapsed of progressive solid tumor, lymphoma, or leukemia in children and adolescents aage 3-18 years | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-018752-27 | Sponsor Protocol Number: UMCN-AKF 10.01 | Start Date*: 2010-11-19 | ||||||||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
| Full Title: Pharmacokinetics of anidulafungin (Ecalta ®) given intravenously as antifungal prophylaxis to recipients of an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or... | ||||||||||||||||||
| Medical condition: Pharmacokinetics of anidulafungin (Ecalta ®) given intravenously as antifungal prophylaxis to recipients of an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-000981-40 | Sponsor Protocol Number: SWEAML12-A | Start Date*: 2013-01-23 | |||||||||||||||||||||
| Sponsor Name:The Swedish AML Group | |||||||||||||||||||||||
| Full Title: Azacitidine compared to conventional chemotherapy in consolidation of elderly patients (> 65 years) with AML in first complete remission | |||||||||||||||||||||||
| Medical condition: | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2008-004932-19 | Sponsor Protocol Number: OMB110911 | Start Date*: 2009-01-27 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Limited | ||||||||||||||||||||||||||||||||||||||
| Full Title: A phase III, open label, randomized, multicenter trial of Ofatumumab added to Chlorambucil vs. Chlorambucil Monotherapy in previously untreated patients with Chronic Lymphocytic Leukemia | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Chronic Lymphocytic Leukaemia | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) IE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) SE (Completed) BE (Prematurely Ended) CZ (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) GR (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2013-003604-39 | Sponsor Protocol Number: MC-FludT.17/M | Start Date*: 2014-04-11 | ||||||||||||||||||||||||||
| Sponsor Name:medac GmbH | ||||||||||||||||||||||||||||
| Full Title: Clinical phase II trial to describe the safety and efficacy of Treosulfan-based conditioning therapy prior to allogeneic haematopoietic stem cell transplantation in paediatric patients with haemato... | ||||||||||||||||||||||||||||
| Medical condition: Male and female children with haematologic malignant diseases as acute lymphoblastic leukaemias (ALL), acute myeloid leukaemias (AML), myelodysplastic syndromes (MDS) and juvenile myelomonocytic le... | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) PL (Completed) AT (Completed) CZ (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2005-005321-63 | Sponsor Protocol Number: DSC/05/2357/15 | Start Date*: 2006-03-13 | |||||||||||
| Sponsor Name:ITALFARMACO | |||||||||||||
| Full Title: Multicentre, open label, uncontrolled, pilot, phase II study of oral ITF2357 in subjects with acute myeloid leukemia refractory/resistant and/or not suitable for any alternative therapy | |||||||||||||
| Medical condition: Acute myeloid leukemia AML (any French-American-British [FAB] type with the exception of M3 subtype, acute promyelocytic leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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