All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Ongoing | 2005-005794-29 | Traitement des syndromes myélodysplasiques par l'association aracytine et bortezomib | not-yet-due | |
Ongoing | 2007-000246-13 | A phase II study of the efficacity and the safety of lenalidomide in subjects with intermediate or the high risk myelodysplastic syndromes (MSD) associated with a deletion (Del) 5q[31] | not-yet-due | |
Exempt | 2007-002212-26 | A Phase I/II Study of Vorinostat in Combination with Low Dose Ara-C for Patients with Intermediate-2 or High Risk Myelodysplastic Syndromes | not-yet-due | |
Ongoing | 2008-000470-21 | A Phase II study of Decitabine in patients with Chronic Myelomonocytic Leukemia | not-yet-due | |
Completed, but no date | 2008-004541-29 | A phase II Study of Azacitidine (Vidaza®) combined to Epoetin beta (NeoRecormon®) in IPSS low-risk and intermediate-1 MDS Patients, resistant to ESA | bad-data | |
Exempt | 2008-005999-28 | PHASE I-II TRIAL OF ERLOTINIB IN HIGHER RISK MYELODYSPLASTIC SYNDROME | not-yet-due | |
Completed, but no date | 2008-006032-36 | A phase ii study of the efficacy and safety of lenalidomide combined to escalating doses of chemotherapy in intermediate-2-or high risk MDS and AML with del 5 q31 | bad-data | |
Completed, but no date | 2008-008262-12 | 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 intermedi... | bad-data | |
Not reported | 2009-011160-11 | A phase II study of the efficacy and safety of lenalidomide combined to azacitidine in intermediate-2 or high risk MDS AND AML with del 5q | 2016-07-25 | due-trials |
Ongoing | 2009-011161-87 | Treatment of anemia in myelodysplastic syndromes low risk with epoetin beta with Analysis of impact on quality of life and functional capacity | not-yet-due | |
Exempt | 2009-013404-32 | A Phase I/II Multicenter Study of IV Clofarabine In Patients with High-Risk Myelodysplastic Syndrome who have failed Therapy with Azacitidine: the NIDEVOL study | not-yet-due | |
Exempt | 2009-017178-19 | A phase I-II study of the efficacy and safety of Idarubicin combined to Azacitidine in int-2 or high risk myelodysplastic syndromes | 2016-05-09 | not-yet-due |
Exempt | 2010-019709-41 | 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/interleuk... | not-yet-due | |
Exempt | 2010-020341-27 | 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 | not-yet-due | |
Exempt | 2012-003120-21 | A phaseI-II trial of acadesine in ipss high and int 2 myelodysplastic syndromes, acute myeloid leukemia with 20-30% marrow blasts and chronic myelomonocytic leukemia type 2 not responding to azacitidi... | not-yet-due | |
Not reported | 2014-000098-38 | A phase II trial of SGI-110 in patients with ipss high and int 2 myelodysplastic syndrome, acute myeloid leukemia with 20-30% marrow blasts and chronic myelomonocytic leukemia type 2 not responding to... | 2018-04-23 | due-trials |
Listed as ongoing, but also has a completion date | 2014-000200-10 | A Randomized Phase III study of Decitabine (DAC) with or without Hydroxyurea (HY) versus HY in patients with advanced proliferative Chronic Myelomonocytic Leukemia (CMML) | 2021-08-16 | bad-data |
Other | 2017-000812-41 | A RANDOMIZED TRIAL TESTING EARLY VERSUS LATE ONSET OF EPO ALFA TREATMENT IN LOWER RISK MDS WITH NON RBC TRANSFUSION DEPENDENT ANEMIA AND WITHOUT DEL 5Q Etude randomisée évaluant l’introduction préc... | not-yet-due | |
Ongoing | 2017-003681-27 | A single-arm phase II multicenter study of IDH1 (AG 120) inhibitor in patients with IDH1 mutated myelodysplastic syndrome Studio multicentrico di fase II a singolo braccio dell'inibitore di IDH1 (A... | not-yet-due | |
Ongoing | 2018-001693-25 | A single-arm phase II multicenter study of IDH2 (AG 221) inhibitor in patients with IDH2 mutated myelodysplastic syndrome | not-yet-due | |
Other | 2019-003685-40 | 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 Étude prospe... | not-yet-due | |
Ongoing | 2020-003400-13 | A Phase 2, Open-Label, Single Arm, Multi-Center Study to Assess the Efficacy and Safety of BST-236 as a Single Agent in Adults Unfit for Intensive Chemotherapy with Relapsed or Refractory Acute Myeloi... | not-yet-due | |
Exempt | 2021-000596-37 | A randomized phase I/ II multicenter study evaluating combination of luspatercept in LR-MDS without RS having failed or being ineligible to ESA Étude multicentrique de phase I/II randomisée évaluan... | not-yet-due | |
Other | 2021-002007-35 | Phase II study with safety run-in of Azacitidine (AZA) combined with Venetoclax (VEN) in patients with higher-risk Chronic Myelomonocytic Leukemia (CMML) Étude de phase II avec phase pilote de tolé... | not-yet-due |