- Trials with a EudraCT protocol (311)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
311 result(s) found for: Myelodysplastic syndrome.
Displaying page 1 of 16.
EudraCT Number: 2004-002935-23 | Sponsor Protocol Number: GIMEMA MDS 0104 | Start Date*: 2004-11-24 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL ADULTO | |||||||||||||
Full Title: Phase II study of PS341 VELCADE in myelodysplastic syndromes MDS. | |||||||||||||
Medical condition: Patients with MDS | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001321-28 | Sponsor Protocol Number: AISSM02A | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:AISSM ONLUS | |||||||||||||
Full Title: Phase II multicenter study of association of arsenic trioxide (ATO) and ascorbic acid in myelodisplastic syndromes | |||||||||||||
Medical condition: Myelodisplastyc Syndrome treatment | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001774-27 | Sponsor Protocol Number: AISSM03 | Start Date*: 2005-05-23 | |||||||||||
Sponsor Name:AISSM ONLUS | |||||||||||||
Full Title: CAMPATH-1H AS IMMUNOSUPPRESSIVE AGENT IN MDS PATIENTS MULTICENTRIC PILOT STUDY | |||||||||||||
Medical condition: In this study we want to assess the potential of CAMPATH-1H as an immunosuppressive agent in a series of selected MDS patients, because T lymphocytes are thought to play an important role in the ... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001516-24 | Sponsor Protocol Number: 20060197 | Start Date*: 2007-08-23 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open Label Extension Study Evaluating the Safety of Long Term Dosing of Romiplostim in Thrombocytopenic Subjects with Myelodysplastic Syndromes (MDS) | |||||||||||||
Medical condition: Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) SE (Prohibited by CA) BE (Completed) DE (Completed) ES (Completed) HU (Completed) PL (Completed) CZ (Completed) AT (Completed) SK (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006147-31 | Sponsor Protocol Number: GIMEMA MDS 0306 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: An open multicenter clinical trial to evaluate the safety, tolerability and efficacy of Deferasirox (ICL670) in patients affected by Myelodysplastic syndrome and transfusional chronic hemosiderosis. | |||||||||||||
Medical condition: Low and intermediate I risk (IPSS score) Myelodysplastic syndrome and transfusion-induced hemosiderosis. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000727-13 | Sponsor Protocol Number: 20130113 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: Single arm, Companion Study to Myelodysplastic Syndrome (MDS) 20090160 Using Darbepoetin alfa for the Treatment of Anaemic Subjects With Myelodysplastic Syndrome | |||||||||||||
Medical condition: Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003997-25 | Sponsor Protocol Number: MDS0519 | Start Date*: 2020-06-10 | ||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||
Full Title: Prospective randomized study on the feasibility of allogeneic stem cell transplantation in higher-risk-myelodysplastic syndromes, performed upfront or preceded by azacitidine or conventional chemot... | ||||||||||||||||||
Medical condition: Higher-risk-myelodysplastic syndromes | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004452-20 | Sponsor Protocol Number: KCH-BMT-06-1.0 | Start Date*: 2007-03-01 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: Pilot study of Reduced Intensity Haematopoietic Stem Cell Transplantation in Patients with Poor Risk Myelodysplastic Syndrome and Acute Myeloid Leukaemia utilising conditioning with Fludarabine, Bu... | |||||||||||||
Medical condition: Myelodysplastic Syndrome Acute myeloid leukaemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011161-87 | Sponsor Protocol Number: GFM-EPO-QoL | Start Date*: 2010-01-13 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: Treatment of anemia in myelodysplastic syndromes low risk with epoetin beta with Analysis of impact on quality of life and functional capacity | |||||||||||||
Medical condition: patients with IPSS low- and intermediate-1 risk myelodysplastic syndromes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000246-62 | Sponsor Protocol Number: CICL670AAU01 | Start Date*: 2016-03-07 | |||||||||||
Sponsor Name:Novartis | |||||||||||||
Full Title: A Study of Magnetic Resonance Imaging Assessment of Cardiac and Liver Iron Load in Patients With Haemoglobinopathies, Myelodysplastic Syndromes (MDS) or Other Anaemias Treated With Exjade® (Deferas... | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003971-11 | Sponsor Protocol Number: CICL670ADE03 | Start Date*: 2007-04-10 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A one-year, open-label, single arm, multi-center trial evaluating the efficacy and safety of oral ICL670 in patients diagnosed with Low and INT-1 risk Myelodysplastic Syndrome (MDS) and transfusion... | |||||||||||||
Medical condition: myelodysplastic syndrome and transfusion-dependent iron overload | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005999-28 | Sponsor Protocol Number: GFM-Erlotinib-08 | Start Date*: 2010-02-04 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | |||||||||||||
Full Title: PHASE I-II TRIAL OF ERLOTINIB IN HIGHER RISK MYELODYSPLASTIC SYNDROME | |||||||||||||
Medical condition: HIGH-RISK MYELODYSPLASTIC SYNDROME (MDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019673-15 | Sponsor Protocol Number: BMT-AZA | Start Date*: 2010-07-15 | |||||||||||
Sponsor Name:Universit� Cattolica del Sacro Cuore | |||||||||||||
Full Title: A open label, phase 2, non randomized, multicentre trial to assess the feasibility of induction treatment with 5-azacitidine (5-AZA) followed by allogeneic stem cell transplantation (allo-SCT) or ... | |||||||||||||
Medical condition: myelodysplastic syndrome (MDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008262-12 | Sponsor Protocol Number: GFM-Len-Epo-08 | Start Date*: 2009-10-05 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A phase II study evaluating the efficacy and safety of Lenalidomide (Revlimid®) with or without Epoetin beta (NeoRecormon®) in transfusion-dependent ESA-resistant patients with IPSS low- and interm... | |||||||||||||
Medical condition: patients with IPSS low- and intermediate-1 risk myelodysplastic syndromes without chromosome 5 abnormality | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014768-21 | Sponsor Protocol Number: TUD-TEMDS1-042 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Dresden Technical University | |||||||||||||
Full Title: Treatment of MDS patients with single agent temsirolimus – a pilot study | |||||||||||||
Medical condition: Myelodysplastic Syndromes (MDS) (20 IPSS LOW+INT-1 and 20 IPSS INT-2+HIGH or proliferating CMML) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017178-19 | Sponsor Protocol Number: GFM- Aza-Ida-09 | Start Date*: 2010-09-14 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A phase I-II study of the efficacy and safety of Idarubicin combined to Azacitidine in int-2 or high risk myelodysplastic syndromes | |||||||||||||
Medical condition: Myelodysplastic syndromes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019709-41 | Sponsor Protocol Number: GFM-Aza-ceplene | Start Date*: 2010-10-13 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A phase I study of azacitidine with Ceplene/interleukin-2 followed by a randomized phase II study of the efficacy and safety of maintenance treatment with azacitidine with or without Ceplene/interl... | |||||||||||||
Medical condition: Myelodysplastic syndromes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003986-20 | Sponsor Protocol Number: LUCAS | Start Date*: 2021-09-06 | |||||||||||
Sponsor Name:Leipzig University | |||||||||||||
Full Title: A Phase II, Open-Label, Multicenter Study of Orally Administered CA-4948 for the Treatment of Anemia in Patients with Very Low, Low or Intermediate Risk Myelodysplastic Syndromes (MDS) | |||||||||||||
Medical condition: Anemia in patients with very low, low or intermediate risk myelodysplastic syndromes (MDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002532-28 | Sponsor Protocol Number: ThymoHEMO1206 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: A Phase II Study of Efficacy of Rabbit Antithymocyte Globulin (rATG) in patients with Low and Itermediate-1 Risk Mylodysplastic Syndrome | |||||||||||||
Medical condition: Low And Intermediate-1 Risk Myelodysplastic Syndrome in adult patients 70 years or younger | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) FR (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020341-27 | Sponsor Protocol Number: GFM-Aza intensif | Start Date*: 2010-06-22 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A phase I/II study of the efficacy and safety of an intensified schedule of Azacitidine (Vidaza®) in intermediate-2 and high risk MDS patients | |||||||||||||
Medical condition: Myelodysplastic syndromes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
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. |
