- 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 3 of 21.
EudraCT Number: 2010-019377-15 | Sponsor Protocol Number: TUD-ETAL-1-045 | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Randomisierte Studie zur allogenen hämatopoetischen Stammzelltransplantation im Vergleich zur Standardchemotherapie bei Patienten in erster kompletter Remission im Alter von <=60 Jahren mit AML int... | |||||||||||||
Medical condition: Hematopoietic stem cell transplantation in patients with newly diagnoses AML ≤60 years of age in intermediate risk, after first complete response in comparison to standard consolidation chemotherap... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004710-41 | Sponsor Protocol Number: AMLBFM0401 | Start Date*: 2006-11-26 | |||||||||||
Sponsor Name:St. Anna Kinderkrebsforschung | |||||||||||||
Full Title: Multizentrische Therapieoptimierungsstudie AML-BFM 2004 zur Behandlung der akuten myeloischen Leukämien bei Kindern und Jugendlichen Multicentric therapy optimizing study AML-BFM 2004 for the trea... | |||||||||||||
Medical condition: For acute myeloic leukaemia in children and juveniles improvment of treatment with new medications should be investigated: 1. Cladribine: originally licenced for hairy cell leukamia has shown good ... | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005872-42 | Sponsor Protocol Number: 0103-007 | Start Date*: 2007-01-31 | |||||||||||
Sponsor Name:Pharmion GmbH | |||||||||||||
Full Title: A Phase II study of MGCD0103 (MG-0103) in patients with acute myelogenous leukemia/high risk MDS who are elderly and have previously untreated disease or who are adult and have relapsed/refractory ... | |||||||||||||
Medical condition: Acute myelogenous leukemia or high risk myelodysplastic syndromes in patients who are elderly and have previously untreated disease or who are adult and have relapsed or refractory disease. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005562-39 | Sponsor Protocol Number: P060205 | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: ALFA 0703 : A Randomized Multicenter Phase III Study to Evaluate the Role of All-trans Retinoic Acid (ATRA) in Combination with Chemotherapy or azacitidine as salvage therapy and Azacitidine as Mai... | |||||||||||||
Medical condition: Older patients with acute myeloblastic leukemia (AML). | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002983-32 | Sponsor Protocol Number: CLBH589B2213 | Start Date*: 2009-06-16 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase II Study of Oral Single Agent Panobinostat in Patients with Refractory de novo or secondary Acute Myelogenous Leukemia (AML) | |||||||||||||
Medical condition: Patients with refractory de novo or secondary acute myelogenous leukemia (AML) | |||||||||||||
|
|||||||||||||
Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) FR (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018418-53 | Sponsor Protocol Number: CSTI571A2110 | Start Date*: 2010-06-01 | ||||||||||||||||
Sponsor Name:Novartis Pharma Service AG | ||||||||||||||||||
Full Title: A non-randomized, open-label study to characterize the pharmacokinetics of Glivec/Gleevec® (imatinib mesylate) in pediatric (age range 1 to less than 4 years) patients with chronic myeloid leukemia... | ||||||||||||||||||
Medical condition: Chronic Myeloid Leukemia (CML) and Philadelphia chromosome positive Acute Lymphoblastic Leukemia (Ph+ ALL) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) NL (Prematurely Ended) HU (Completed) DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001082-15 | Sponsor Protocol Number: IPC2006-07 | Start Date*: 2008-07-31 | |||||||||||
Sponsor Name:Institut Paoli Calmette | |||||||||||||
Full Title: Etude de Phase I-II multicentrique de l'association Cloretazine-Daunorubicine-Aracytine dans le traitement des leucémies aigües myéloïdes du groupe cytogénétique défavorable. | |||||||||||||
Medical condition: Malades atteints de Leucémie Aigüe Myéloïde | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020432-18 | Sponsor Protocol Number: LAMAN-01AN | Start Date*: 2011-05-03 | |||||||||||
Sponsor Name:ASOCIACION ANDALUZA DE HEMATOLOGIA Y HEMOTERAPIA | |||||||||||||
Full Title: TRATAMIENTO DE MANTENIMIENTO CON 5-AZACITIDINA EN PACIENTES CON LEUCEMIA MIELOBLÁSTICA AGUDA NO ELEGIBLES PARA TRATAMIENTO INTENSIVO Y CON RESPUESTA PARCIAL O COMPLETA TRAS QUIMIOTERAPIA DE INDUCCIÓN | |||||||||||||
Medical condition: PACIENTES CON LEUCEMIA MIELOBLÁSTICA AGUDA NO ELEGIBLES PARA TRATAMIENTO INTENSIVO Y CON RESPUESTA PARCIAL O COMPLETA TRAS QUIMIOTERAPIA DE INDUCCIÓN | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001430-14 | Sponsor Protocol Number: peg-filgrastim Vs filgrastim nel t | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Peg-filgrastim Vs filgrastrim in pediatric patients. | |||||||||||||
Medical condition: haematologic malignant tumors | |||||||||||||
|
|||||||||||||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004968-40 | Sponsor Protocol Number: TUD-SORAML-034 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized, multi-center phase II trial to assess the efficacy of Sorafenib added to standard primary therapy in patients with newly diagnosed AML ≤ 60 years of age | |||||||||||||
Medical condition: Sorafenib added to standard primary therapy in patients with newly diagnosed AML ≤ 60 years of age | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003581-34 | Sponsor Protocol Number: DASATINIB compassionate use | Start Date*: 2006-07-27 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: DASATINIB compassionate use | |||||||||||||
Medical condition: CML and Ph | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004050-16 | Sponsor Protocol Number: HEAT-AML | Start Date*: 2019-08-01 | |||||||||||
Sponsor Name:University Hospital Karolinska | |||||||||||||
Full Title: HEAT-AML (Hydroxyurea-Enhanced Ara-C Treatment of Adult Acute Myeloid Leukaemia): A phase I/II multicenter study to assess the tolerability and efficacy of the addition of hydroxyurea to standard a... | |||||||||||||
Medical condition: Newly diagnosed acute myeloid leukaemia (AML) in patients ≥ 18 years of age | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003482-28 | Sponsor Protocol Number: SGN33A-005 | Start Date*: 2016-07-14 | |||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
Full Title: A randomized, double-blind phase 3 study of vadastuximab talirine (SGN-CD33A) versus placebo in combination with azacitidine or decitabine in the treatment of older patients with newly diagnosed ac... | |||||||||||||
Medical condition: Acute myeloid leukemia (AML) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) HU (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) BE (Completed) AT (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000981-40 | Sponsor Protocol Number: SWEAML12-A | Start Date*: 2013-01-23 | |||||||||||||||||||||
Sponsor Name:The Swedish AML Group | |||||||||||||||||||||||
Full Title: Azacitidine compared to conventional chemotherapy in consolidation of elderly patients (> 65 years) with AML in first complete remission | |||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002487-27 | Sponsor Protocol Number: 1230.14 | Start Date*: 2013-01-21 | |||||||||||
Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
Full Title: A phase III randomised, double-blind, controlled, parallel group study of intravenous volasertib in combination with subcutaneous low-dose cytarabine vs. placebo + low-dose cytarabine in patients ≥... | |||||||||||||
Medical condition: previously untreated acute myeloid leukaemia in patients ≥ 65 years and ineligible for intensive remission induction therapy | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) PT (Completed) GR (Completed) AT (Completed) FI (Completed) ES (Completed) IT (Completed) CZ (Completed) NL (Completed) HU (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003624-37 | Sponsor Protocol Number: CA180-188 | Start Date*: 2007-11-16 | |||||||||||||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: Dasatinib in Chronic Myelogenous Leukemia or Philadelphia Chromosome Positive Acute Lymphoblastic Leukemic Subjects Who are Experiencing Clinical Benefit on Current START or CA180039 Protocols: Lon... | |||||||||||||||||||||||
Medical condition: Chronic Myelogenous Leukemia or Philadelphia Chromosome Positive Acute Lymphoblastic Leukemic Subjects. | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) IE (Completed) GB (Completed) IT (Completed) FI (Completed) ES (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003617-27 | Sponsor Protocol Number: 1230.4 | Start Date*: 2008-11-07 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: An open phase I/IIa trial to investigate the maximum tolerated dose, safety, pharmacokinetics, and efficacy of intraveneous BI 6727 as monotherapy or in combination with subcutaneous cytarabine in... | |||||||||||||
Medical condition: patients with acute myeloid leukaemia (AML) that are not eligible for intensive treatment | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004761-17 | Sponsor Protocol Number: SG033-0003 | Start Date*: 2008-05-14 | |||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
Full Title: A Phase IIB, Randomized, Double-Blinded, Placebo-Controlled Study of Low Dose Cytarabine and Lintuzumab Compared to Low Dose Cytarabine and Placebo in Patients 60 Years of Age and Older with Previo... | |||||||||||||
Medical condition: acute myeloid leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) HU (Prematurely Ended) AT (Completed) PL (Prematurely Ended) BG (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001076-38 | Sponsor Protocol Number: GMI-1271-301 | Start Date*: 2018-12-21 | |||||||||||
Sponsor Name:GlycoMimetics, Inc. | |||||||||||||
Full Title: A Phase III Randomized, Double-Blind Trial to Evaluate the Efficacy of Uproleselan Administered with Chemotherapy versus Chemotherapy Alone in Patients with Relapsed/Refractory Acute Myeloid Leukemia | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) NL (Prematurely Ended) ES (Ongoing) IT (Prematurely Ended) FR (Prematurely Ended) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
