- Trials with a EudraCT protocol (455)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
455 result(s) found for: Acute Myeloid Leukemia (AML).
Displaying page 11 of 23.
EudraCT Number: 2008-001043-19 | Sponsor Protocol Number: CLO-34100405 | Start Date*: 2008-09-24 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: Phase III Randomized, Double-Blind, Controlled Study Comparing Clofarabine and Cytarabine versus Cytarabine Alone in Adult Patients 55 Years and Older with Acute Myelogenous Leukemia (AML) who have... | |||||||||||||
Medical condition: Acute Myelogenous (Myeloid) Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003111-10 | Sponsor Protocol Number: D-00272-CT2014002 | Start Date*: 2016-06-01 | ||||||||||||||||
Sponsor Name:Cell Medica Ltd | ||||||||||||||||||
Full Title: A single arm Phase I/II study of the safety and efficacy of gene-modified WT1 TCR therapy in patients with myelodysplastic syndrome (MDS) or acute myeloid leukaemia (AML) who have failed to achieve... | ||||||||||||||||||
Medical condition: Acute myeloid leukaemia and myelodysplastic syndromes in adults | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000971-15 | Sponsor Protocol Number: PLERIFLAG | Start Date*: 2011-09-23 | |||||||||||
Sponsor Name:PETHEMA | |||||||||||||
Full Title: Multicentric, prospective, open-label, of one group and phase I-II clinical trial to analyze induction treatment with a combination of fludarabine, idarubicin, cytarabine, G-CSF and plerixafor for ... | |||||||||||||
Medical condition: Relapsed or resistant acute myeloid leukemia (AML). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005159-14 | Sponsor Protocol Number: GC P#02.01.001 | Start Date*: 2008-04-15 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Gamida Cell-Teva Joint Venture Ltd. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Multi-Center, Multi-National, Historical Cohort Controlled Study to Evaluate Efficacy and Safety of Transplantation of StemEx, Umbilical Cord Blood Stem and Progenitor Cells Expanded Ex Vivo, in ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: High-risk haematological malignancies (including AML, ALL, CML, NHL, HD, and MDS) with an indication for allogeneic haematopoietic stem cell transplantation, to support haematopoietic reconstitutio... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Completed) IT (Completed) HU (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001371-20 | Sponsor Protocol Number: 200170 | Start Date*: 2013-09-06 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||||||||||||||||||
Full Title: Study 200170: A Rollover Study to Provide Continued Treatment with Eltrombopag | ||||||||||||||||||
Medical condition: Acute myelogenous leukemia & Idiopathic thrombocytopenic purpura (ITP | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) ES (Completed) BE (Completed) GR (Completed) PL (Completed) NL (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000380-46 | Sponsor Protocol Number: 75276617ALE1003 | Start Date*: 2022-12-27 | |||||||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||||||||||||
Full Title: A Phase I/Ib Study of JNJ-75276617 in Combination with Conventional Chemotherapy for Pediatric and Young Adult Participants with Relapsed/Refractory Acute Leukemias Harboring KMT2A, NPM1, or Nucleo... | |||||||||||||||||||||||
Medical condition: Relapsed/Refractory Acute Leukemias Harboring KMT2A, NPM1, or Nucleoporin Gene Alterations | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011613-24 | Sponsor Protocol Number: HOVON102AML/SAKK30/09 | Start Date*: 2010-01-25 | ||||||||||||||||||||||||||
Sponsor Name:HOVON Foundation | ||||||||||||||||||||||||||||
Full Title: Randomized study with a run-in feasibility phase to assess the added value of Clofarabine in combination with standard remission-induction chemotherapy in patients aged 18-65 years with previously ... | ||||||||||||||||||||||||||||
Medical condition: - a cytopathologically confirmed diagnosis of AML according WHO classification (excluding acute promyelocytic leukaemia) or - a diagnosis of refractory anemia with excess of blasts (RAEB) and ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) SE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-004461-41 | Sponsor Protocol Number: CR-AIR-007 | Start Date*: 2013-06-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of ATIR, donor T-lymphocytes depleted ex vivo of host alloreactive T-cells, in patients with a hematologic malignan... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with a hematologic malignancy (AML, ALL, or MDS) who are eligible for a haploidentical HSCT | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000684-24 | Sponsor Protocol Number: B1371003 | Start Date*: 2013-03-12 | ||||||||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
Full Title: A Phase 1B/2 Study To Evaluate The Safety And Efficacy of PF-04449913, An Oral Hedgehog Inhibitor, In Combination With Intensive Chemotherapy, Low Dose ARA-C Or Decitabine In Patients With Acute My... | ||||||||||||||||||
Medical condition: Acute myeloid leukemia or myelodysplastic syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017098-40 | Sponsor Protocol Number: DEC-MDS | Start Date*: 2010-07-09 | |||||||||||||||||||||||||||||||
Sponsor Name:King's College London [...] | |||||||||||||||||||||||||||||||||
Full Title: Use of Decitabine in Myelodysplastic Syndrome (MDS) Following Azacitidine (AZA) Failure (DEC-MDS) | |||||||||||||||||||||||||||||||||
Medical condition: Myelodysplastic Syndromes Acute Myeloid Leukaemia Chronic Myelomonocytic Leukaemia | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002430-21 | Sponsor Protocol Number: PALOMA | Start Date*: 2019-07-17 | ||||||||||||||||
Sponsor Name:GWT-TUD GmbH | ||||||||||||||||||
Full Title: Primary comparison of Liposomal Anthracycline based treatment versus conventional care strategies prior to allogeneic stem cell transplantation in patients with higher risk MDS and oligoblastic AML | ||||||||||||||||||
Medical condition: Untreated patients with higher risk MDS and oligoblastic AML eligible and intended for allogeneic HCT within the next 6 months | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017376-25 | Sponsor Protocol Number: MEK111759 | Start Date*: 2011-03-15 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: An Open-Label, Dose-Escalation, Phase I/II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor GSK1120212 in Subjects with Relapsed or Ref... | |||||||||||||
Medical condition: Relapsed or refractory leukemias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000450-31 | Sponsor Protocol Number: NMDSG07A | Start Date*: 2007-06-20 | ||||||||||||||||
Sponsor Name:The Nordic MDS group | ||||||||||||||||||
Full Title: A multicentre phase II study of the efficacy and safety of lenalidomide in high-risk myeloid disease (high-risk MDS and AML) with a karyotype including del(5q) or monosomy 5. | ||||||||||||||||||
Medical condition: High risk Myelodysplastic Syndrome (IPSS Int-2 or High) or Acute Myeloid Leukemia with a karyotype including del(5q) or monosomy 5 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001209-64 | Sponsor Protocol Number: BRD 06/10-I | Start Date*: 2007-08-16 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Nantes | |||||||||||||
Full Title: Etude multicentrique de phase III randomisée ouverte testant l’efficacité du gemtuzumab ozogamycin (MYLOTARG®) en association avec la chimiothérapie intensive chez les patients de 18 à 60 ans attei... | |||||||||||||
Medical condition: leucémie aiguë myéloblastique (LAM) avec cytogénétique intermédiaire | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005163-26 | Sponsor Protocol Number: P060504 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude de phase 3 comparant une chimiothérapie d'induction séquentielle systématique à une chimiothérapie d'induction séquentielle conditionnelle chez des patients atteints d'une Leucémie Aigüe Myél... | |||||||||||||
Medical condition: Leucémie Aiguë Myéloïde de pronostic favorable de l'adulte du groupe CBF. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003386-28 | Sponsor Protocol Number: GH29914 | Start Date*: 2016-05-11 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase Ib/II multi-arm study with venetoclax in combination with cobimetinib, and venetoclax in combination with idasanutlin in patients ≥ 60 years with relapsed or refractory acute myeloid leukem... | |||||||||||||
Medical condition: Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001588-22 | Sponsor Protocol Number: AML003 | Start Date*: 2019-07-04 | |||||||||||
Sponsor Name:Rafael Pharmaceuticals, Inc. | |||||||||||||
Full Title: Phase III Multicenter Open-Label Randomized Trial to Evaluate Efficacy and Safety of CPI-613 in Combination with High Dose Cytarabine and Mitoxantrone (CHAM) Compared to High Dose Cytarabine and Mi... | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002011-24 | Sponsor Protocol Number: 42205525 | Start Date*: 2008-05-22 |
Sponsor Name:European Group for Blood and Marrow Transplantation (EBMT) | ||
Full Title: Dose-reduced versus standard conditioning followed by allogeneic stem cell transplantation in patients with MDS or sAML: A randomised phase III study | ||
Medical condition: Myelodysplastic syndromes and secondary acute myeloid leukaemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) BE (Completed) GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002793-47 | Sponsor Protocol Number: MKIA-088-001 | Start Date*: 2019-01-16 | ||||||||||||||||
Sponsor Name:NERVIANO MEDICAL SCIENCES SRL | ||||||||||||||||||
Full Title: A Phase I/II Study of NMS-03592088, a FLT3, KIT and CSF1R Inhibitor, in Patients with Relapsed or Refractory AML or CMML | ||||||||||||||||||
Medical condition: Acute myeloidleukemia (AML) or chronic myelomonocytic leukemia (CMML) relapsed or refractory. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000440-18 | Sponsor Protocol Number: CD-TCR-001 | Start Date*: 2017-12-19 | ||||||||||||||||||||||||||
Sponsor Name:Medigene AG | ||||||||||||||||||||||||||||
Full Title: A Phase I/II, Open-Label, Non-Randomized, Multicentre, Dose-Escalation Clinical Trial with Control Group to Evaluate the Safety, Feasibility and Preliminary Efficacy of PRAME TCR Modified T Cells, ... | ||||||||||||||||||||||||||||
Medical condition: High Risk Myeloid Neoplasms | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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