- Trials with a EudraCT protocol (816)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
816 result(s) found for: Acute toxicity.
Displaying page 1 of 41.
EudraCT Number: 2007-005806-29 | Sponsor Protocol Number: AKH-AML-0108 | Start Date*: 2008-05-23 | |||||||||||
Sponsor Name:Medical University of Vienna, Dep. of Internal Medicine I, division of Hematology & Hemostaseology | |||||||||||||
Full Title: Evaluation of Efficacy and Toxicity of Intensified Consolidation Therapy in AML Patients ≥60 Years | |||||||||||||
Medical condition: Acute myeloid leukemia (AML), de novo, FAB classification other than M3 or WHO classification other than APL t(15,17), > 60 years, abesence of any other antededent hematologic disease of >8 months,... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000334-19 | Sponsor Protocol Number: 702 | Start Date*: 2012-08-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE S. SALVATORE | |||||||||||||
Full Title: Phase II multicenter study of low dose Cytarabine + Tosedostat for previously untreated older patients with acute myeloid leukemia (AML) | |||||||||||||
Medical condition: Untreated patients aged 60> years with Acute Myeloid Leukemia | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000526-37 | Sponsor Protocol Number: SAIL | Start Date*: 2014-08-18 | ||||||||||||||||||||||||||
Sponsor Name:GSO Global Clinical Research B.V. | ||||||||||||||||||||||||||||
Full Title: An Investigator-Initiated Study To Evaluate Ara-C and Idarubicin in Combination with the Selective Inhibitor Of Nuclear Export (SINE) Selinexor (KPT-330) in Patients with Relapsed Or Refractory A... | ||||||||||||||||||||||||||||
Medical condition: Patients with relapsed/refractory Acute Myeloid Leukemia (AML) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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: 2017-004110-25 | Sponsor Protocol Number: TUD-PEMAZA-068 | Start Date*: 2018-12-14 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: MRD-guided treatment with pembrolizumab and azacitidine in NPM1mut AML patients with an imminent hematological relapse | |||||||||||||
Medical condition: Patients with NPM1mut AML >= 18 years in CR presenting with MRD after conventional chemotherapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006852-37 | Sponsor Protocol Number: CPKC412A2301 | Start Date*: 2008-07-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase III randomized, double-blind study of induction(daunorubicin/cytarabine)and consolidation (high dose cytarabine) chemotherapy + midostaurin (PKC412) or placebo in newly diagnosed patients <... | |||||||||||||
Medical condition: newly diagnosed FLT3 mutated acute myeloid leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) AT (Completed) CZ (Completed) NL (Completed) SK (Completed) HU (Completed) BE (Completed) IT (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005248-26 | Sponsor Protocol Number: AML 07 | Start Date*: 2008-05-29 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. MARIA DELLA MISERICORDIA | |||||||||||||
Full Title: INDUCTION, CONSOLIDATION AND INTENSIFICATION PROTOCOL FOR PATIENTS YOUNGER THAN 66 YEARS WITH PREVIOUSLY UNTREATED CD33 POSITIVE ACUTE MYELOID LEUKEMIA (AML) | |||||||||||||
Medical condition: newly diagnosed (untreated) and CD 33 positive AML, under 66 years. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
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 | |||||||||||||
|
|||||||||||||
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: 2012-001594-93 | Sponsor Protocol Number: IPH2102-201 | Start Date*: 2013-05-15 | |||||||||||
Sponsor Name:Innate Pharma | |||||||||||||
Full Title: Double-Blind Placebo-Controlled Randomized Phase 2 Study of IPH2102 as Maintenance Treatment in Elderly patients with Acute Myeloid Leukemia (AML) in First Complete Remission | |||||||||||||
Medical condition: Acute Myeloid Leukemia in Elderly patients in First Complete Remission | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002986-30 | Sponsor Protocol Number: CLBH589B2116 | Start Date*: 2010-01-08 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase Ib, open-label, multi-center dose-finding study of oral panobinostat (LBH589) in combination with ara-C and mitoxantrone as salvage therapy for refractory or relapsed acute myeloid leukemia | |||||||||||||
Medical condition: refractory or relapsed acute myeloid leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001588-78 | Sponsor Protocol Number: SPON CU 125 | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: AML16 Pilot Trial: A Phase1/2 Trial to assess the feasibility of combining Clofarabine with daunorubicin and Daunorubicin + Clofarabine with Mylotarg in older patients with Acute Myeloid Leukaemia ... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006295-11 | Sponsor Protocol Number: ICOG-2007 | Start Date*: 2008-04-07 | |||||||||||
Sponsor Name:Instituto de Investigación del Hospital de la Santa Creu i Sant Pau | |||||||||||||
Full Title: TREATMENT OF PRIMARY ACUTE MYELOID LEUKEMIA WITH THE COMBINATION OF IDARUBICIN, CYTARABINE AND GEMTUZUMAB OZOGAMYCIN (MYLOTARG) ASSOCIATED OR NOT TO G-CSF PRIMING: PROSPECTIVE STUDY OF EFFICACY AND... | |||||||||||||
Medical condition: Leucemia Mieloide Aguda Primaria "de novo" | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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: 2008-004583-40 | Sponsor Protocol Number: 101010 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universitaetsklinikum Muenster | |||||||||||||
Full Title: A randomized, multi-center phase II trial to assess the efficay of 5-azacytidine added to standard primery therapy in elderly patients with newly diagnosed AML. | |||||||||||||
Medical condition: The disease under investigation is newly diagnosed Acute Myeloid Leucemia (AML) in elderly patients. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004503-11 | Sponsor Protocol Number: DACO-016 | Start Date*: 2006-09-14 | ||||||||||||||||
Sponsor Name:Eisai Medical Research Inc. | ||||||||||||||||||
Full Title: Randomized Phase 3 Trial of Decitabine Versus Patient's Choice with Physician's Advice of Either Supportive Care or Low-dose Cytarabine for the Treatment of Older Patients with Newly Diagnosed Acut... | ||||||||||||||||||
Medical condition: Acute Myloid Leukemia | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) ES (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
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: 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 | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002026-78 | Sponsor Protocol Number: GRASPA-AML-2012-01 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:ERYTECH Pharma | |||||||||||||
Full Title: A Multicentre, open, randomized, controlled phase IIb trial evaluating efficacy and tolerability of GRASPA (L-asparaginase encapsulated in red blood cells) plus low-dose cytarabine vs low-dose cyta... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FI (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002331-41 | Sponsor Protocol Number: HaploMUDStudy | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:University Medical Center Hamburg - Eppendorf | |||||||||||||
Full Title: Matched Unrelated vs. Haploidentical Donor for Allogeneic Stem Cell Transplantation in Patients with Acute Leukemia with Identical GVHD Prophylaxis – A Randomized Prospective European Trial | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000018-39 | Sponsor Protocol Number: AMLBFM2012 | Start Date*: 2014-11-20 | |||||||||||
Sponsor Name:Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH gGmbH) | |||||||||||||
Full Title: Clinical trial for the treatment of acute myeloid leukemia in children and adolescents | |||||||||||||
Medical condition: AML | |||||||||||||
|
|||||||||||||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
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. |
