- Trials with a EudraCT protocol (63)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (17)
63 result(s) found for: aml.
Displaying page 1 of 4.
EudraCT Number: 2011-005023-40 | Sponsor Protocol Number: RG_11-182 | Start Date*: 2013-05-22 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: ROMAZA: Phase I trial of combination therapy with romidepsin and azacitidine in patients with newly diagnosed, relapsed or refractory Acute Myeloid Leukaemia ineligible for conventional chemotherapy | |||||||||||||
Medical condition: Acute myeloid leukaemia (AML) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005207-32 | Sponsor Protocol Number: RG_11-187 | Start Date*: 2012-06-08 | |||||||||||
Sponsor Name:The University of Birmingham | |||||||||||||
Full Title: Phase II Randomised Trial of 5-Azacitidine versus 5-Azacitidine in combination with Vorinostat in patients with Relapsed Acute Myeloid Leukaemia ineligible for Intensive Chemotherapy | |||||||||||||
Medical condition: Haematological Malignancy - Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007043-14 | Sponsor Protocol Number: RHMCAN0638 | Start Date*: 2010-09-21 | ||||||||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | ||||||||||||||||||
Full Title: A Pilot Study of Clofarabine Pre-Conditioning Prior to Full or Reduced Intensity Allogeneic Transplantation in the Treatment of High Risk Acute Myeloid Leukaemia and Myelodysplasia | ||||||||||||||||||
Medical condition: High risk Acute Myeloid Leukaemia and Myelodysplasia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003857-73 | Sponsor Protocol Number: D6130C00003 | Start Date*: 2019-09-26 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase I/II, Open-Label, Multicentre 2-Part Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of AZD2811 as Monotherapy or in Combination in Treatment-Naïve or Relapsed/Refr... | ||
Medical condition: Treatment Naïve or Relapsed/Refractory Acute Myeloid Leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2013-000341-39 | Sponsor Protocol Number: RG_12-268 | Start Date*: 2013-07-23 | |||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||
Full Title: A Phase Ib Study of Eltrombopag and Azacitidine in Patients with High Risk Myelodysplastic Syndromes and Related Disorders | |||||||||||||||||||||||
Medical condition: High-risk Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukaemia (CMML-2) and Acute Myeloid Leukaemia (AML) with less than 30% blasts. | |||||||||||||||||||||||
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Population Age: Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001918-13 | Sponsor Protocol Number: Hovon 43 | Start Date*: 2008-01-17 |
Sponsor Name:University of Wales College of Medicine | ||
Full Title: Randomised induction and post induction therapy in older patients (>=61 years of age) with acute myeloid leukaemia (AML) and refractory anaemia with excess blasts (RAEB, RAEB-t) | ||
Medical condition: Acute Myeloid Leukaemia (AML) Refractory Anaemia with Excesss Blasts (RAEB) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2018-001012-30 | Sponsor Protocol Number: RG_18-048 | Start Date*: 2019-05-02 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: A Double-Blind, Phase III, Randomised Study to Compare the Efficacy and Safety of Oral Azacitidine (CC-486) Versus Placebo in Subjects with Acute Myeloid Leukaemia or Myelodysplastic Syndromes as M... | ||||||||||||||||||
Medical condition: Acute Myeloid Leukaemia (AML) and Myelodysplasia (MDS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005889-38 | Sponsor Protocol Number: UCL/10/0411 | Start Date*: 2012-08-29 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University College London | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A UK multicentre phase II study of haploidentical stem cell transplantation in patients with haematological malignancies | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute myeloid leukaemia Myelodysplastic syndromes Therapy related AML or MDS Philadelphia positive Chronic Myeloid Leukaemia Acute lymphoblastic leukaemia Non-Hodgkin's lymphoma (follicular lymphom... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002419-24 | Sponsor Protocol Number: RG_19-116 | Start Date*: 2020-09-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:The University of Birmingham | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A multi-centre phase II trial of GvHD prophylaxis following unrelated donor stem cell transplantation comparing Thymoglobulin vs. Calcineurin inhibitor or Sirolimus-based post-transplant cyclophosp... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukaemia, Acute lymphoblastic leukaemia, Chronic myelomonocytic leukemia, Myelodysplastic syndromes, Non-Hodgkin lymphoma, Hodgkin lymphoma, Multiple myeloma, Chronic lymphocytic leu... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001600-29 | Sponsor Protocol Number: ARO-013 | Start Date*: 2018-06-13 | ||||||||||||||||
Sponsor Name:Arog Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: Phase III Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy of the Addition of Crenolanib to Salvage Chemotherapy Versus Salvage Chemotherapy Alone in Subjects ≤ 75 Year... | ||||||||||||||||||
Medical condition: Relapsed/Refractory FLT3 Mutated Acute Myeloid Leukemia (AML) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Ongoing) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001051-32 | Sponsor Protocol Number: 2102-HEM-101 | Start Date*: 2019-03-14 | |||||||||||||||||||||
Sponsor Name:Forma Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: A Phase 1/2, Multicenter, Open-label Study of FT 2102 as a Single Agent and in Combination with Azacitidine or Cytarabine in Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome with an... | |||||||||||||||||||||||
Medical condition: Relapsed/refractory Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000168-53 | Sponsor Protocol Number: EP0042-101 | Start Date*: 2020-07-29 | |||||||||||||||||||||
Sponsor Name:Ellipses Pharma Limited | |||||||||||||||||||||||
Full Title: A Modular, Multipart, Multi-arm, Open-label, Phase I/IIa Study to Evaluate the Safety and Tolerability of EP0042 Alone and in Combination with Anti-cancer Treatments in Patients with Advanced Malig... | |||||||||||||||||||||||
Medical condition: Acute myeloid leukaemia (AML), Chronic myelomonocytic leukaemia (CMML) and Myelodysplastic syndrome (MDS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000273-24 | Sponsor Protocol Number: RG_19-282 | Start Date*: 2020-10-06 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Venetoclax or Intensive Chemotherapy for Treatment Of Favourable Risk Acute Myeloid Leukaemia: A Molecularly Guided Phase 2 Study | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002301-61 | Sponsor Protocol Number: 2215-CL-0603 | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. (APGD) | |||||||||||||
Full Title: A Phase 1/2, Multicenter, Open-Label, Single Arm, Dose Escalation and Expansion Study of Gilteritinib (ASP2215) Combined with Chemotherapy in Children, Adolescents and Young Adults with FMS-like Ty... | |||||||||||||
Medical condition: FMS-like Tyrosine Kinase 3 (FLT3)/Internal Tandem Duplication (ITD) Positive Relapsed or Refractory Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002730-21 | Sponsor Protocol Number: SPON1227-13 | Start Date*: 2013-11-25 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A Trial for Older Patients with Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
Medical condition: Acute Myeloid Leukaemia High Risk Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000749-19 | Sponsor Protocol Number: SPON934-11 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: Bloodwise and NCRI Working Group Pick a Winner Programme (LI-1) Trial | |||||||||||||
Medical condition: Acute myeloid leukemia and high-risk myelodysplastic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002477-56 | Sponsor Protocol Number: IMGN632-0802 | Start Date*: 2020-01-08 | |||||||||||
Sponsor Name:ImmunoGen, Inc. | |||||||||||||
Full Title: A Phase 1b/2 Study of IMGN632 as Monotherapy or Combination with Venetoclax and/or Azacitidine for Patients with CD123-Positive Acute Myeloid Leukemia | |||||||||||||
Medical condition: CD123 positive Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003813-11 | Sponsor Protocol Number: CP-MGD006-01 | Start Date*: 2016-07-14 | ||||||||||||||||
Sponsor Name:MacroGenics, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2, First-in-Human, Dose Escalation Study of MGD006, a CD123 x CD3 Dual Affinity Re-Targeting (DART) Bi-Specific Antibody-Based Molecule, in Patients with Relapsed or Refractory Acute Myel... | ||||||||||||||||||
Medical condition: Relapsed or Refractory Acute Myeloid Leukemia or Intermediate-2/High Risk Myelodysplastic Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005066-30 | Sponsor Protocol Number: RG_14-088 | Start Date*: 2018-03-20 | |||||||||||
Sponsor Name:The University of Birmingham | |||||||||||||
Full Title: MyeChild 01: International Randomised Phase III Clinical Trial in Children with Acute Myeloid Leukaemia - Incorporating an Embedded Dose Finding Study for Gemtuzumab Ozogamicin in Combination with ... | |||||||||||||
Medical condition: Newly diagnosed acute myeloid leukaemia (AML), high risk myelodysplastic syndrome(MDS) and isolated myeloid sarcoma (either de novo or secondary) are eligible for the trial. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005584-10 | Sponsor Protocol Number: 103 PH GL 2007 CL003 | Start Date*: 2008-02-27 | ||||||||||||||||
Sponsor Name:Pharmion Corporation [...] | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Open-Label Study of Single Agent Azacitidine (Vidaza®) vs. Single Agent MGCD0103 vs. Azacitidine in Combination With MGCD0103 for the Treatment of Elderly Subjects With Newly... | ||||||||||||||||||
Medical condition: Newly diagnosed Acute Myeloid Leukemia and Intermediate-2, or high-risk Myelodysplastic Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Ongoing) SE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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