- 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 7 of 21.
EudraCT Number: 2009-014462-26 | Sponsor Protocol Number: DB-AML-01 | Start Date*: 2010-05-04 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Dutch-Belgian pediatric AML protocol for children with newly diagnosed acute myeloid leukemia, based on the NOPHO-AML 2004 study | |||||||||||||
Medical condition: Acute Myeloid Leukemia in children | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2014-001876-75 | Sponsor Protocol Number: HOVON103AMLSelinexor | Start Date*: 2016-10-28 | |||||||||||||||||||||
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 selinexor (KPT-330) to standard induction chemotherapy in AML and high r... | |||||||||||||||||||||||
Medical condition: patients ≥ 66 years with: - a diagnosis of AML and related precursor neoplasms according to WHO 2008 classification (excluding acute promyelocytic leukemia) including secondary AML (after an antec... | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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: 2016-000327-10 | Sponsor Protocol Number: SAMBA | Start Date*: 2016-11-03 | ||||||||||||||||
Sponsor Name:GWT-TUD GmbH | ||||||||||||||||||
Full Title: SINGLE AGENT JNJ-56022473 IN MDS AND AML PATIENTS FAILING HYPOMETHYLATING AGENT BASED THERAPY | ||||||||||||||||||
Medical condition: AML and MDS patients failing or being refractory to hypomethylating agent (HMA) treatment. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000508-13 | Sponsor Protocol Number: 72779 | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:Princess Máxima Center for Pediatric Oncology | |||||||||||||
Full Title: An open-label, randomized clinical trial on teicoplanin infection prophylaxis in pediatric patients with acute myeloid leukemia | |||||||||||||
Medical condition: Acute myeloid leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003803-11 | Sponsor Protocol Number: CHUBX 2007/13 | Start Date*: 2007-10-24 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Essai multicentrique randomisé ouvert évaluant l'apport du CCNU dans le traitement des leucémies aigues myéloïdes (LAM) des sujets de plus de 60 ans à cytogénétique non défavorable et la faisabilit... | |||||||||||||
Medical condition: Dans cette étude est évalué l'apport de la Belustine chez des patients porteurs d'une leucémie aiguë myéloïde (LAM) de plus de 60 ans à cytogénétique défavorable et la faisabilité de l'allogreffe à... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000282-68 | Sponsor Protocol Number: AML-PG03 | Start Date*: 2017-12-20 | |||||||||||
Sponsor Name:PROF.BRUNANGELO FALINI,DR.SSA MARIA PAOLA MARTELLI,UNIVERSITA' DI PERUGIA | |||||||||||||
Full Title: A phase 2a study of the clinical activity and safety of actinomycin D in patients with NPM1-wild type AML (other than APL) aged = 70 years old and/or unfit for intensive chemotherapy, either newly ... | |||||||||||||
Medical condition: patients with NPM1-wild type AML (other than APL) aged >= 70 years old and/or unfit for intensive chemotherapy, either newly diagnosed or previously treated with hypometylating agents | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003817-42 | Sponsor Protocol Number: NILG-AML 02/06 | Start Date*: 2006-09-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI RIUNITI DI BERGAMO A.O. DI RILIEVO NAZIONALE | |||||||||||||
Full Title: A phase III trial in adult acute myelogenous leukemia AML comparing 1 standard-dose versus high-dose remission induction therapy and 2 , within a risk-oriented postremission strategy, an autolo... | |||||||||||||
Medical condition: PATIENT WHIT LMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002610-23 | Sponsor Protocol Number: M14-387 | Start Date*: 2015-02-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 1/2 Study of Venetoclax in Combination with Low-Dose Cytarabine in Treatment-Naïve Subjects with Acute Myelogenous Leukemia Who Are ≥ 60 Years of Age and Who Are Not Eligible for Standard A... | |||||||||||||
Medical condition: Acute Myelogenous Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013669-25 | Sponsor Protocol Number: AEG35156-206 | Start Date*: 2009-12-18 | |||||||||||
Sponsor Name:Aegera Therapeutics Inc. | |||||||||||||
Full Title: An Open-Label Randomized Phase 2 Study of the X-Linked Inhibitor of Apoptosis (XIAP) Antisense AEG35156 Given in Combination with High-dose Cytarabine and Idarubicin in AML Following Failure of a S... | |||||||||||||
Medical condition: Acute myeloid leukemia after failure of a single standard dose cytarabine based frontline induction regimen. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004724-34 | Sponsor Protocol Number: PRAN-16-52 | Start Date*: 2017-08-11 | |||||||||||
Sponsor Name:Helsinn Healthcare SA | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo-Controlled, Multicenter, Randomized Study Of Pracinostat In Combination With Azacitidine In Patients ≥18 Years With Newly Diagnosed Acute Myeloid Leukemia Unfit F... | |||||||||||||
Medical condition: Newly diagnosed Acute Myeloid Leukemia patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) HU (Completed) ES (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006114-20 | Sponsor Protocol Number: AML2420 | Start Date*: 2021-09-28 | ||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||
Full Title: A Phase 2, prospective, multi-center intervention trial in patients with acute myeloid leukemia secondary to myeloproliferative neoplasms unfit for intensive chemotherapy investigating a treatment ... | ||||||||||||||||||
Medical condition: Acute Myeloid Leukemia secondary to myeloproliferative neoplasms | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003124-44 | Sponsor Protocol Number: DKMS-14-01 | Start Date*: 2015-01-15 | ||||||||||||||||
Sponsor Name:DKMS gemeinnützige GmbH | ||||||||||||||||||
Full Title: Evaluation of the impact of remission induction chemotherapy prior to allogeneic stem cell transplantation in relapsed and poor-response patients with AML | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002365-37 | Sponsor Protocol Number: 3066K1-1165 | Start Date*: 2012-04-04 | |||||||||||
Sponsor Name:J.W. Goethe-University | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized, multicenter phase II trial to assess the efficacy of temsirolimus added to standard primary therapy in elderly patients with newly diagnosed AML | |||||||||||||
Medical condition: Patients with newly diagnosed AML (except APL) according to the FAB and WHO classification, including AML evolving from MDS and AML after previous cytotoxic therapy or radiation (secondary AML) Bo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019718-25 | Sponsor Protocol Number: AML-CLOFARA-CA09 | Start Date*: 2010-08-19 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: Ensayo clínico multicéntrico, prospectivo, abierto, de un solo grupo, de fase II para analizar la terapia de inducción con una combinación de clofarabina y dosis bajas de citarabina seguido de tera... | |||||||||||||
Medical condition: Leucemia Mieloblástica Aguda | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001381-14 | Sponsor Protocol Number: CSTI5710109E2 | Start Date*: 2005-08-02 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II study to determine the safety and the anti- leukemic effects of STI571 in adults patients with Philadelphia chromosome positive leukemia including acute lymphoblastic le... | |||||||||||||
Medical condition: Philadelphia chromosome positive leukemia including acute lymphoblastic leukemia, acute myeloid leukemia and accelerate phase myeloid leukemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000241-35 | Sponsor Protocol Number: PXD101-CLN-15 | Start Date*: 2007-06-22 | |||||||||||
Sponsor Name:TopoTarget A/S | |||||||||||||
Full Title: A Phase I/II Clinical Trial of PXD101 in Combination with Idarubicin in Patients with AML Not Suitable for Standard Intensive Therapy | |||||||||||||
Medical condition: Patients with AML in need of new treatment principles | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012346-23 | Sponsor Protocol Number: AZA-AML-001 | Start Date*: 2010-07-14 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, OPEN-LABEL, STUDY OF AZACITIDINE (VIDAZA®)VERSUS CONVENTIONAL CARE REGIMENS FOR THE TREATMENT OF OLDER SUBJECTS WITH NEWLY DIAGNOSED ACUTE MYELOID LEUKEMIA | |||||||||||||
Medical condition: Newly diagnosed de novo Acute Myeloid Leukemia (AML) or AML secondary to prior myelodysplastic disease in older subjects with >30% bone marrow blasts and who are not eligible for hematopoietic ste... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) BE (Completed) FR (Completed) GB (Completed) ES (Completed) NL (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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