- Trials with a EudraCT protocol (406)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
406 result(s) found for: Acute myeloid leukaemia.
Displaying page 4 of 21.
EudraCT Number: 2019-003117-33 | Sponsor Protocol Number: Pevonedistat-2002 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||||||||||||
Full Title: A Randomized, Open-label, Controlled, Phase 2 Study of Pevonedistat, Venetoclax, and Azacitidine Versus Venetoclax Plus Azacitidine in Adults With Newly Diagnosed Acute Myeloid Leukemia Who Are Unf... | |||||||||||||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) IT (Trial now transitioned) FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002288-14 | Sponsor Protocol Number: HM1006 | Start Date*: 2009-02-10 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: Phase I Dose Escalation Study of Clofarabine and Liposomal Daunorubicin in Childhood and Adolescent AML | ||||||||||||||||||
Medical condition: Paediatric patients (6 months to 18 years) diagnosed with AML who are refractory to front line therapy, early first relapse (less than 1 year from diagnosis) and second and subsequent relapse patie... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002847-14 | Sponsor Protocol Number: CU 106 | Start Date*: 2005-12-16 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: AML16; A National Cancer Research Institute Trial in Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndromes | |||||||||||||
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) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014455-68 | Sponsor Protocol Number: HOVON103AMLTosedostat | Start Date*: 2010-08-16 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: A randomized phase II multicenter study with a safety run-in to assess the tolerability and efficacy of the addition of oral tosedostat to standard induction therapy in AML and RAEB ≥ 66 years and ... | |||||||||||||||||||||||
Medical condition: patients ≥ 66 years.with a confirmed diagnosis of o AML (not APL) (see appendix A) or o refractory anemia with excess of blasts (RAEB) with an IPSS score ≥ 1.5 OR Patients of any age ≥ 1... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) NO (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013094-17 | Sponsor Protocol Number: HOVON103AMLLEN | Start Date*: 2010-04-13 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: A randomized phase II multicenter study with a safety run-in to assess the tolerability and efficacy of the addition of oral lenalidomide to standard induction therapy in AML and RAEB ≥ 66 years an... | |||||||||||||||||||||||
Medical condition: patients ≥ 66 years.with a confirmed diagnosis of o AML (not APL) (see appendix A) or o refractory anemia with excess of blasts (RAEB) with an IPSS score ≥ 1.5 OR Patients of any age ≥ 1... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) NO (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002361-17 | Sponsor Protocol Number: AML2521 | Start Date*: 2021-11-17 | ||||||||||||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||||||||||||
Full Title: A multicentric phase 2 study of venetoclax and azacitidine for the management of the molecular relapse/progression in adult NPM1- mutaded acute myeloid leukemia. | ||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukemia with NPM1 mutation. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010114-30 | Sponsor Protocol Number: D1531C00009 | Start Date*: 2009-06-23 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, open-label, multi-centre, 2-stage, parallel group study to assess the efficacy, safety and tolerability of AZD1152 alone and in combination with low dose cytosine arabinoside (LDAC) i... | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) FR (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000872-14 | Sponsor Protocol Number: UCL/11/0519 | Start Date*: 2013-07-23 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: Adoptive Immunotherapy with CD25/71 allodepleted donor T cells to improve immunity after unrelated donor stem cell transplant (ICAT) | ||||||||||||||||||
Medical condition: acute myeloid or acute lymphoblastic leukaemia | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003025-28 | Sponsor Protocol Number: TUD-RELAX1-070 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Phase-I/II trial for relapsed or refractory AML patients combining cytarabine and mitoxantrone with venetoclax | |||||||||||||
Medical condition: Patients 18-75 years with acute myeloid leukaemia (AML) at first or second relapse after intensive chemotherapy including allogeneic stem cell transplantation or primary refractory to standard indu... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005684-10 | Sponsor Protocol Number: 1247.3 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Boehringer Ingelheim España S.A. | |||||||||||||
Full Title: Ensayo clínico abierto de fase I/IIa para evaluar la dosis máxima tolerada, eficacia, seguridad y farmacocinética de BI 811283 en combinación con citarabina en pacientes con leucemia mieloide aguda... | |||||||||||||
Medical condition: Pacientes con leucemia mieloide aguda no tratados previamente y que no sean elegibles para tratamiento intensivo Previously untreated acute myeloid leukaemia in adult patients that are not eligibl... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001721-29 | Sponsor Protocol Number: SPD758-216 | Start Date*: 2005-12-05 |
Sponsor Name:SGX Pharmaceuticals, Inc. | ||
Full Title: An Open-Label, Single-Arm, Multi-Center, Phase II/III study of Troxatyl (Troxacitabine) Administered by Continuous Infusion in Patients with Acute Myeloid Leukemia (AML) in second salvage | ||
Medical condition: Acute Myeloid Leukemia (AML) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000018-39 | Sponsor Protocol Number: AMLBFM2012 | Start Date*: 2014-11-20 | |||||||||||
Sponsor Name:Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH gGmbH) | |||||||||||||
Full Title: Clinical trial for the treatment of acute myeloid leukemia in children and adolescents | |||||||||||||
Medical condition: AML | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005241-20 | Sponsor Protocol Number: F14512IN102G1 | Start Date*: 2013-02-18 | |||||||||||
Sponsor Name:Pierre Fabre Medicament | |||||||||||||
Full Title: Phase I-II study of F14512 in combination with cytarabine in patients 60 years old and older with acute myeloid leukemia. | |||||||||||||
Medical condition: The scope of this study is the treatment of patient acute myeloid leukaemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003191-12 | Sponsor Protocol Number: TUD-2DAUNO-058 | Start Date*: 2014-01-31 | ||||||||||||||||||||||||||
Sponsor Name:Technische Universität Dresden | ||||||||||||||||||||||||||||
Full Title: Randomized comparison between two dose levels of daunorubicin and between one versus two cycles of in-duction therapy for adult patients with acute myeloid leukemia ≤65 years | ||||||||||||||||||||||||||||
Medical condition: Newly diagnosed AML other than acute promyelocytic leukemia (APL) according to WHO criteria, i.e. bone marrow aspirate or biopsy must contain ≥20% blasts of all nucleated cells or differential bloo... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023499-25 | Sponsor Protocol Number: 1230.25 | Start Date*: 2011-06-16 | |||||||||||||||||||||
Sponsor Name:
[...]
1.
2. Boehringer Ingelheim AB |
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Full Title: A phase II/III randomized, open-label study to compare the efficacy and safety of intravenous volasertib in combination with subcutaneous cytarabine versus investigator’s choice of anti-leukemic t... | |||||||||||||||||||||||
Medical condition: Relapsed or refractory acute myeloid leukemia in adult patients who are considered not to benefit from / not to be eligible for intensive salvage therapy and/or stem cell transplantation and have n... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) BE (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) NL (Completed) FI (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004427-38 | Sponsor Protocol Number: 0001A3-300-GL | Start Date*: 2009-01-28 | |||||||||||
Sponsor Name:Antisoma Research Ltd. | |||||||||||||
Full Title: Phase 3 Open-Label Randomized Study of Amonafide L-Malate in Combination with Cytarabine Compared to Daunorubicin in Combination with Cytarabine in Patients with Secondary Acute Myeloid Leukemia (AML) | |||||||||||||
Medical condition: secondary acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Ongoing) AT (Prematurely Ended) HU (Prematurely Ended) EE (Prematurely Ended) CZ (Completed) GB (Prematurely Ended) ES (Prematurely Ended) BE (Completed) IT (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004440-12 | Sponsor Protocol Number: CPKC412A2408 | Start Date*: 2017-11-12 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: An open-label, multicenter, Phase IIIb study to assess the safety and efficacy of midostaurin (PKC412) in patients 18 years of age or older with newly-diagnosed FLT3-mutated Acute Myeloid Leukemia ... | |||||||||||||
Medical condition: newly diagnosed FLT3 mutated acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) CZ (Completed) ES (Ongoing) HU (Completed) FR (Completed) BG (Completed) GR (Completed) SK (Completed) LT (Completed) IT (Completed) EE (Completed) HR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002026-78 | Sponsor Protocol Number: GRASPA-AML-2012-01 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:ERYTECH Pharma | |||||||||||||
Full Title: A Multicentre, open, randomized, controlled phase IIb trial evaluating efficacy and tolerability of GRASPA (L-asparaginase encapsulated in red blood cells) plus low-dose cytarabine vs low-dose cyta... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FI (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021961-61 | Sponsor Protocol Number: VOS-AML-301 | Start Date*: 2011-05-19 | ||||||||||||||||
Sponsor Name:Sunesis Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Controlled, Double Blind, Multinational Clinical Study of the Efficacy and Safety of Vosaroxin and Cytarabine Versus Placebo and Cytarabine in Patients With First Relapsed or... | ||||||||||||||||||
Medical condition: Relapsed or refractory acute myeloid leukemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) BE (Completed) HU (Completed) ES (Completed) IT (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002983-18 | Sponsor Protocol Number: ICT-8 | Start Date*: 2017-05-08 | |||||||||||
Sponsor Name:Hybrigenics S.A. | |||||||||||||
Full Title: Efficacy Study of Inecalcitol in Combination with Decitabine in Acute Myeloid Leukemia Patients Unfit for Standard Chemotherapy | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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