- Trials with a EudraCT protocol (555)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (79)
555 result(s) found for: Acute Lymphoblastic Leukemia.
Displaying page 5 of 28.
EudraCT Number: 2013-004773-27 | Sponsor Protocol Number: AALL08B1 | Start Date*: 2014-03-07 | |||||||||||
Sponsor Name:Children's Oncology Group | |||||||||||||
Full Title: Classification of Newly Diagnosed Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006541-14 | Sponsor Protocol Number: ema3_pegAML | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: A phase II pilot trial to evaluate the efficacy of treatment with Pegilate G-CSF in a group of elderly patients AML without chemotherapy indications | |||||||||||||
Medical condition: acute mieloid leukemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005248-26 | Sponsor Protocol Number: AML 07 | Start Date*: 2008-05-29 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. MARIA DELLA MISERICORDIA | |||||||||||||
Full Title: INDUCTION, CONSOLIDATION AND INTENSIFICATION PROTOCOL FOR PATIENTS YOUNGER THAN 66 YEARS WITH PREVIOUSLY UNTREATED CD33 POSITIVE ACUTE MYELOID LEUKEMIA (AML) | |||||||||||||
Medical condition: newly diagnosed (untreated) and CD 33 positive AML, under 66 years. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002983-32 | Sponsor Protocol Number: CLBH589B2213 | Start Date*: 2009-06-16 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase II Study of Oral Single Agent Panobinostat in Patients with Refractory de novo or secondary Acute Myelogenous Leukemia (AML) | |||||||||||||
Medical condition: Patients with refractory de novo or secondary acute myelogenous leukemia (AML) | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) FR (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024264-18 | Sponsor Protocol Number: MT103-205 | Start Date*: 2011-11-23 | |||||||||||
Sponsor Name:Amgen Research (Munich) GmbH | |||||||||||||
Full Title: A Single-Arm Multicenter Phase II Study preceded by Dose Evaluation to Investigate the Efficacy, Safety, and Tolerability of the BiTE® Antibody Blinatumomab (MT103) in Pediatric and Adolescent Pati... | |||||||||||||
Medical condition: Pediatric and adolescent patients with B-precursor ALL in second or later bone marrow relapse, in any marrow relapse after allogeneic HSCT, or refractory to other treatments. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) IT (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001588-78 | Sponsor Protocol Number: SPON CU 125 | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: AML16 Pilot Trial: A Phase1/2 Trial to assess the feasibility of combining Clofarabine with daunorubicin and Daunorubicin + Clofarabine with Mylotarg in older patients with Acute Myeloid Leukaemia ... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001082-15 | Sponsor Protocol Number: IPC2006-07 | Start Date*: 2008-07-31 | |||||||||||
Sponsor Name:Institut Paoli Calmette | |||||||||||||
Full Title: Etude de Phase I-II multicentrique de l'association Cloretazine-Daunorubicine-Aracytine dans le traitement des leucémies aigües myéloïdes du groupe cytogénétique défavorable. | |||||||||||||
Medical condition: Malades atteints de Leucémie Aigüe Myéloïde | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004710-41 | Sponsor Protocol Number: AMLBFM0401 | Start Date*: 2006-11-26 | |||||||||||
Sponsor Name:St. Anna Kinderkrebsforschung | |||||||||||||
Full Title: Multizentrische Therapieoptimierungsstudie AML-BFM 2004 zur Behandlung der akuten myeloischen Leukämien bei Kindern und Jugendlichen Multicentric therapy optimizing study AML-BFM 2004 for the trea... | |||||||||||||
Medical condition: For acute myeloic leukaemia in children and juveniles improvment of treatment with new medications should be investigated: 1. Cladribine: originally licenced for hairy cell leukamia has shown good ... | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006475-36 | Sponsor Protocol Number: RG_07-187 | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Phase ll Study of the Adjunctive Use of Azacitidine in Patients Undergoing Reduced Intensity Allogeneic Transplantation for Acute Myeloid Leukaemia | |||||||||||||
Medical condition: Patients who have Acute Myeloid Leukaemia (AML) will be recruited to this trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004836-39 | Sponsor Protocol Number: Initial-1 | Start Date*: 2017-11-01 | |||||||||||
Sponsor Name: Goethe Universität | |||||||||||||
Full Title: An open label phase II study to evaluate the efficacy and safety of Inotuzumab Ozogamicin for Induction Therapy followed by a conventional chemotherapy based consolidation and maintenance therapy I... | |||||||||||||
Medical condition: Acute lymphoblastic leukemia, Philadelphia-chromosome and BCR-ABL negative disease, patient aged 56 years or older | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001347-37 | Sponsor Protocol Number: GIMEMAAML17(EORTC06012) | Start Date*: 2004-07-30 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Gemtuzumab ozogamicin (GO) combined with standard intensive chemotherapy versus standard intensive chemotherapy alone for induction/consolidation in patients 61-75 years old with previously untre... | |||||||||||||
Medical condition: Previously untreated primary or secondary AML (including AML after MDS).All FAB subtypes except M3.No AML supervening after other myeloproliferative diseases.Age 61-75 years. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004356-39 | Sponsor Protocol Number: GIMEMAAML19(EORTC06031) | Start Date*: 2005-05-16 | |||||||||||
Sponsor Name:E.O.R.T.C. - EUROPEAN ORGANIZATION FOR RESEARCH AND TREATMENT OF CANCER | |||||||||||||
Full Title: Gemtuzumab Ozogamicin (GO) monotherapy versus standard supportive care for previously untreated AML in elderly patients who are not eligible for intensive chemotherapy: a randomized phase II/III tr... | |||||||||||||
Medical condition: Elderly patients (61-75 years not eligible for intensive chemotherapy;age > 75 years), with previously untreated, primary or secondary (no after other myeloproliferative diseases) AML (except M3). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020432-18 | Sponsor Protocol Number: LAMAN-01AN | Start Date*: 2011-05-03 | |||||||||||
Sponsor Name:ASOCIACION ANDALUZA DE HEMATOLOGIA Y HEMOTERAPIA | |||||||||||||
Full Title: TRATAMIENTO DE MANTENIMIENTO CON 5-AZACITIDINA EN PACIENTES CON LEUCEMIA MIELOBLÁSTICA AGUDA NO ELEGIBLES PARA TRATAMIENTO INTENSIVO Y CON RESPUESTA PARCIAL O COMPLETA TRAS QUIMIOTERAPIA DE INDUCCIÓN | |||||||||||||
Medical condition: PACIENTES CON LEUCEMIA MIELOBLÁSTICA AGUDA NO ELEGIBLES PARA TRATAMIENTO INTENSIVO Y CON RESPUESTA PARCIAL O COMPLETA TRAS QUIMIOTERAPIA DE INDUCCIÓN | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001430-14 | Sponsor Protocol Number: peg-filgrastim Vs filgrastim nel t | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Peg-filgrastim Vs filgrastrim in pediatric patients. | |||||||||||||
Medical condition: haematologic malignant tumors | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004968-40 | Sponsor Protocol Number: TUD-SORAML-034 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized, multi-center phase II trial to assess the efficacy of Sorafenib added to standard primary therapy in patients with newly diagnosed AML ≤ 60 years of age | |||||||||||||
Medical condition: Sorafenib added to standard primary therapy in patients with newly diagnosed AML ≤ 60 years of age | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003581-34 | Sponsor Protocol Number: DASATINIB compassionate use | Start Date*: 2006-07-27 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: DASATINIB compassionate use | |||||||||||||
Medical condition: CML and Ph | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000766-30 | Sponsor Protocol Number: HO146 | Start Date*: 2018-03-09 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Blinatumomab added to prephase and consolidation therapy in precursor B-acute lymphoblastic leukemia in adults. A phase II trial. | |||||||||||||
Medical condition: Precursor B-acute lymphoblastic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006978-20 | Sponsor Protocol Number: HBS407 | Start Date*: 2007-11-21 | |||||||||||
Sponsor Name:Talon Therapeutics , Inc. | |||||||||||||
Full Title: A Phase 2 Study to Evaluate the Safety and Efficacy of Weekly Doses of Marqibo® (vincristine sulfate liposomes injection) in Adult Patients with Philadelphia Chromosome-negative Acute Lymphoblastic... | |||||||||||||
Medical condition: Philadelphia Chromosome-negative Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000706-36 | Sponsor Protocol Number: 20120216 | Start Date*: 2013-12-10 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: A Phase 2 Single Arm, Multicenter Trial to Evaluate the Efficacy of the BiTE® Antibody Blinatumomab in Adult Subjects with Relapsed/Refractory Philadelphia Positive B-precursor Acute Lymphoblastic ... | ||||||||||||||||||
Medical condition: Adult patients with relapsed and/or refractory Philadelphia Chromosome- positive B-precursor ALL | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) GB (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018314-75 | Sponsor Protocol Number: MT103-203 | Start Date*: 2010-08-05 | |||||||||||
Sponsor Name:Amgen Research (Munich) GmbH | |||||||||||||
Full Title: A confirmatory multicenter, single-arm study to assess the efficacy, safety, and tolerability of the BiTE® antibody blinatumomab in adult patients with minimal residual disease (MRD) of B-precursor... | |||||||||||||
Medical condition: minimal residual disease (MRD) of B-precursor ALL | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) AT (Completed) ES (Completed) CZ (Completed) FR (Completed) PL (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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