- 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 6 of 21.
EudraCT Number: 2019-003863-23 | Sponsor Protocol Number: TUD-MOSAIC-075 | Start Date*: 2020-07-03 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Midostaurin + Gemtuzumab Ozogamicin combination in first-line standard therapy for acute myeloid leukemia | |||||||||||||
Medical condition: Patients with newly diagnosed acute myeloid leukemia (AML) fit for intensive curative treatment displaying a cytogenetic aberration or fusion transcript in the core-binding factor (CBF) genes or FL... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 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: 2019-003685-40 | Sponsor Protocol Number: GFM-DACORAL-DLI | Start Date*: 2020-12-28 | ||||||||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | ||||||||||||||||||
Full Title: A PHASE II PROSPECTIVE STUDY “GFM-DACORAL-DLI” ASTX727 AND DONOR LYMPHOCYTE INFUSIONS (DLI) AFTER ALLOGENEIC STEM CELL TRANSPLANTATION (ALLO SCT) IN VERY HIGH RISK MDS OR AML PATIENTS | ||||||||||||||||||
Medical condition: Patients with high risk myelodysplastic syndrome or acute myeloid leukemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (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: 2020-002297-26 | Sponsor Protocol Number: NCT04476199 | Start Date*: 2020-11-03 | |||||||||||
Sponsor Name:GITMO GRUPPO ITALIANO PER IL TRAPIANTO DI MIDOLLO OSSEO, CELLULE STAMINALI EMOPOIETICHE E TERAPIA | |||||||||||||
Full Title: Phase II study on Venetoclax (VEN) plus Decitabine (DEC) (VEN-DEC) for elderly (=60 <75years) patients with newly diagnosed Acute Myeloid Leukemia (AML) elegible for allogeneic Stem Cell Transplant... | |||||||||||||
Medical condition: allogeneic transplantation in CR / Cri / MLFS condition | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2007-005803-16 | Sponsor Protocol Number: GITMOAMLR.2 | Start Date*: 2007-12-24 | |||||||||||
Sponsor Name:GITMO (GRUPPO ITALIANO DI MIDOLLLO OSSEO) | |||||||||||||
Full Title: RANDOMIZED STUDY COMPARING INTRAVENOUS BUSULFAN (I.V. BU; BUSILVEX) PLUS FLUDARABINE (BUFLU) VERSUS INTRAVENOUS BUSULFAN PLUS CYCLOPHOSPHAMIDE (BUCY2) AS CONDITIONING REGIMENS PRIOR TO ALLOGENEIC H... | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002042-32 | Sponsor Protocol Number: CPX-351-TA-SMP | Start Date*: 2021-09-16 | |||||||||||
Sponsor Name:FILO | |||||||||||||
Full Title: A phase II study of CPX-351 monotherapy in Acute Myeloid Leukemia secondary to Myeloproliferative neoplams | |||||||||||||
Medical condition: newly secondary AML according to WHO 2016 classification following an antecedent of Myeloproliferative Neoplasm including Essential Thrombocythemia (ET), Polycythemia Vera (PV), primary or secondar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2015-001901-15 | Sponsor Protocol Number: NKCell_LMA_2015 | Start Date*: 2016-04-01 | |||||||||||
Sponsor Name:Antonio Pérez Martínez | |||||||||||||
Full Title: Natural Killer cell infusion as consolidation therapy in children and adolescents with acute myelogenous leukemia. | |||||||||||||
Medical condition: Acute myeloid leukemia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2013-000642-20 | Sponsor Protocol Number: TRC117146 | Start Date*: 2013-08-02 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Randomized, Blinded, Placebo-Controlled, Dose Finding Study to Assess the Safety and Efficacy of the Oral Thrombopoietin Receptor Agonist, Eltrombopag, Administered to Subjects with Acute Myelog... | |||||||||||||
Medical condition: Acute myelogenous leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) PL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003061-19 | Sponsor Protocol Number: CL1-65487-003 | Start Date*: 2021-01-07 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Phase I / II, open label, dose escalation part (phase I) followed by non-comparative expansion part (phase II), multi-centre study, evaluating safety, pharmacokinetics and efficacy of S65487, a Bcl... | |||||||||||||
Medical condition: Previously untreated Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) FR (Trial now transitioned) HU (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2006-000868-83 | Sponsor Protocol Number: CP4055-106 | Start Date*: 2008-04-30 | |||||||||||
Sponsor Name:Clavis Pharma ASA | |||||||||||||
Full Title: A Phase I/II Study of CP-4055 in Patients with Refractory/Relapsed Hematologic Malignancies | |||||||||||||
Medical condition: Phase II. Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
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: 2014-003490-41 | Sponsor Protocol Number: AML-PG02 | Start Date*: 2016-09-09 | |||||||||||
Sponsor Name:PROF.BRUNANGELO FALINI,DR.SSA MARIA PAOLA MARTELLI,UNIVERSITA' DI PERUGIA | |||||||||||||
Full Title: A PHASE 2A STUDY ON THE CLINICAL ACTIVITY AND SAFETY OF ACTINOMYCIN-D IN PATIENTS WITH NPM1-MUTATED AML AGED =70 YEARS AND/OR UNFIT FOR INTENSIVE CHEMOTHERAPY, EITHER NEWLY DIAGNOSED OR PREVIOUSLY ... | |||||||||||||
Medical condition: NPM1-MUTATED AML NEWLY DIAGNOSED OR PREVIOUSLY TREATED WITH HYPOMETHYLATING AGENTS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002864-36 | Sponsor Protocol Number: PKRPC001 | Start Date*: 2021-11-04 | |||||||||||
Sponsor Name:Priothera S.A.S. | |||||||||||||
Full Title: A prospective randomized, double-blind, placebo-controlled, multi-center phase IIb study to evaluate the efficacy and safety of mocravimod in acute myeloid leukemia (AML) patients undergoing alloge... | |||||||||||||
Medical condition: Patients undergoing allogeneic hematopoietic stem cell transplant (HSCT) for acute myeloid leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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