- 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 10 of 28.
EudraCT Number: 2014-000400-99 | Sponsor Protocol Number: PLMA34 | Start Date*: 2014-09-15 | |||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||
Full Title: 10-day decitabine, fludarabine and 2 Gray TBI as conditioning strategy for poor and very poor risk AML in CR1 | |||||||||||||
Medical condition: Acute myeloid leukemia AML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018980-41 | Sponsor Protocol Number: Pediatric_Relapsed_AML2010/01 | Start Date*: 2013-10-15 | |||||||||||
Sponsor Name:German Society of Pediatric Hematology and Oncology gGmbH (GPOH gGmbH) | |||||||||||||
Full Title: International randomized phase III study on the treatment of children and adolescents with refractory or relapsed acute myeloid leukemia | |||||||||||||
Medical condition: Pediatric relapsed or refractory AML | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) HU (Completed) DK (Prematurely Ended) CZ (Prematurely Ended) NL (Ongoing) SE (Prematurely Ended) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003871-20 | Sponsor Protocol Number: AML1819 | Start Date*: 2020-02-26 | ||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||
Full Title: Phase III study to assess the impact of gemtuzumab ozogamicin, in combination with standard chemotherapy, on the levels of minimal residual disease, and the role of glasdegib as a post-transplant m... | ||||||||||||||||||
Medical condition: Favorable-intermediate-risk Acute Myeloid Leukemia (AML) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002448-42 | Sponsor Protocol Number: GMI-1271-201 | Start Date*: 2015-03-12 | |||||||||||
Sponsor Name:GlycoMimetics, Inc. | |||||||||||||
Full Title: A Phase I/II, open-label multicenter study to determine safety, pharmacokinetics and efficacy of GMI-1271 in combination with chemotherapy in patients with acute myeloid leukemia | |||||||||||||
Medical condition: Acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004942-27 | Sponsor Protocol Number: P16/11 | Start Date*: 2017-07-17 | |||||||||||
Sponsor Name:Centre Hospitalier de Versailles | |||||||||||||
Full Title: A Phase 2 Study of Inotuzumab Ozogamicin (INO) Combined to Chemotherapy in Older Patients with Philadelphia Chromosome-negative CD22+ B-cell Precursor Acute Lymphoblastic Leukemia | |||||||||||||
Medical condition: Philadelphia chromosome (Ph)-negative CD22+ B-cell Precursor (BCP) Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003936-21 | Sponsor Protocol Number: AML1919 | Start Date*: 2020-04-09 | ||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||
Full Title: A Phase 3, prospective, randomized multi-center intervention trial of early intensification in AML patients bearing FLT3 mutations based on peripheral blast clearance. A MYNERVA-GIMEMA study. AMEL... | ||||||||||||||||||
Medical condition: Acute Myeloid Leukemia (LMA) with FLT3 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: 2015-002892-30 | Sponsor Protocol Number: 1315.2 | Start Date*: 2016-04-14 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: An open-label, Phase I/II trial to determine the maximum tolerated dose and investigate safety, pharmacokinetics and efficacy of BI 836858 in combination with decitabine in patients with acute myel... | |||||||||||||
Medical condition: patients with acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003150-13 | Sponsor Protocol Number: TUD-DELTA1-063 | Start Date*: 2015-03-31 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: A randomized placebo-controlled phase 2 study of decitabine with or without eltrombopag in AML patients ≥65 years of age not eligible for intensive chemotherapy | |||||||||||||
Medical condition: acute myeloid leukemia AML | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003969-10 | Sponsor Protocol Number: MB-105 | Start Date*: 2018-06-08 | |||||||||||
Sponsor Name:Moleculin Biotech, Inc. | |||||||||||||
Full Title: Phase 1/2 Study of Liposomal Annamycin for the Treatment of Subjects with Acute Myeloid Leukemia (AML) that is Refractory to or Relapsed after Induction Therapy | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000698-54 | Sponsor Protocol Number: 10002 | Start Date*: 2019-11-28 | |||||||||||
Sponsor Name:Prinses Maxima Centrum voor kinderoncologie | |||||||||||||
Full Title: A phase I/II post cord blood HCT dendritic cells vaccination trial directed against WT1 for pediatric and young adult acute myeloid leukemia: the U-DANCE-anti-AML trial | |||||||||||||
Medical condition: AML: Acute Myeloid leukemia/ cancer of blood and bone marrow | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002702-21 | Sponsor Protocol Number: UKH062014 | Start Date*: 2015-07-14 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle- Wittenberg | |||||||||||||
Full Title: A double- blind, placebo controlled, randomized, multicenter, Phase II study to assess the efficacy of BL-8040 addition to consolidation therapy in AML patients | |||||||||||||
Medical condition: consolidation therapy in acute myeloid leukemia in first complete remission | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Temporarily Halted) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003148-31 | Sponsor Protocol Number: P05115 | Start Date*: 2007-10-12 | ||||||||||||||||||||||||||
Sponsor Name:Schering-Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
Full Title: A Phase 4 Study of the Pharmacokinetics of Oral Posaconazole Among Patients with Compromised Gastrointestinal Function and at High Risk for Invasive Fungal Infection. | ||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukemia, Neutropenia, Antifungal Prophylaxis, Gastrointestinal Disorders | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005542-39 | Sponsor Protocol Number: C0701a/501/ON/US | Start Date*: 2006-03-29 |
Sponsor Name:Cephalon Inc. | ||
Full Title: Estudio de extensión abierto del fármaco oral CEP-701 en pacientes con enfermedades malignas hematológicas y no hematológicas que han participado en un estudio clínico del CEP-701 | ||
Medical condition: Patients with hematologic and non hematologic malignancies who have participated in a clinical study of CEP 701 may participate in this extension study. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) SE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001086-41 | Sponsor Protocol Number: UKM10_0014 | Start Date*: 2012-02-28 | |||||||||||
Sponsor Name:University Hospital of Muenster | |||||||||||||
Full Title: A randomized, placebo-controlled, multi-center phase I/II trial to assess the safety and efficacy of nintedanib (BIBF 1120) added to low-dose cytarabine in elderly patients with AML unfit for an in... | |||||||||||||
Medical condition: untreated acute myeloid leukemia patients unfit for an intensive treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 2014-002217-31 | Sponsor Protocol Number: 2215-CL-0101 | Start Date*: 2015-07-09 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
Full Title: A Phase 1/2 Open-Label, Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ASP2215 in Patients with Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
Medical condition: Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018539-16 | Sponsor Protocol Number: KKS-134 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:Philipps-Universität Marburg | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized, multi-center phase II trial to assess the efficacy of Sorafenib-maintenance therapy in Flt3-ITD positive AML in complete hematological remission afte... | |||||||||||||
Medical condition: Flt3-ITD positive AML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008198-73 | Sponsor Protocol Number: CR-AIR-004 | Start Date*: 2010-09-09 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: An open-label, uncontrolled, multicenter, multinational study on the efficacy and safety of administration of donor lymphocytes depleted of alloreactive T-cells (ATIR), through the use of TH9402 an... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with hematologic malignancies who are eligible for an allogeneic stem cell transplantation but without the availability of an (according to the treating physician) suitable matched related... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) NL (Prematurely Ended) BE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002160-34 | Sponsor Protocol Number: ELP1020 | Start Date*: 2008-10-24 | |||||||||||
Sponsor Name:EleosInc Limited | |||||||||||||
Full Title: Aezea™ (cenersen) in combination with chemotherapy for the treatment of refractory acute myelogenous leukemia subjects ≥ 55 years of age with inadequate response to a single frontline induction cou... | |||||||||||||
Medical condition: Refractory acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002743-89 | Sponsor Protocol Number: S0106 | Start Date*: 2007-04-10 | |||||||||||
Sponsor Name:Southwest Oncology Group (SWOG) | |||||||||||||
Full Title: A PHASE III STUDY OF THE ADDITION OF GEMTUZUMAB OZOGAMICIN (MYLOTARG®) DURING INDUCTION THERAPY VERSUS STANDARD INDUCTION WITH DAUNOMYCIN AND CYTOSINE ARABINOSIDE FOLLOWED BY CONSOLIDATION AND SUBS... | |||||||||||||
Medical condition: Previously untreated de novo acute myeloid leukemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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