- Trials with a EudraCT protocol (199)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
199 result(s) found for: Myelodysplastic Syndromes (MDS).
Displaying page 8 of 10.
EudraCT Number: 2011-005934-20 | Sponsor Protocol Number: ALLO-WT1/IPC2011-006 | Start Date*: 2013-06-12 | |||||||||||||||||||||
Sponsor Name:Institut Paoli-Calmettes | |||||||||||||||||||||||
Full Title: | |||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002935-27 | Sponsor Protocol Number: ADVL1712 | Start Date*: 2021-05-21 | |||||||||||||||||||||
Sponsor Name:National Cancer Institute | |||||||||||||||||||||||
Full Title: A Feasibility Trial of MLN4924 (Pevonedistat,TAK924) Given in Combination With Azacitidine, Fludarabine, and Cytarabine, in Children, Adolescents, and Young Adults With Relapsed or Refractory Acute... | |||||||||||||||||||||||
Medical condition: This trial studies the side effects and how well pevonedistat, azacitidine, fludarabine phosphate, and cytarabine work in treating patients with acute myeloid leukemia that has come back or has not... | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000547-34 | Sponsor Protocol Number: QoL-ESC RevMDS | Start Date*: 2008-06-09 | |||||||||||
Sponsor Name:ASSOCIAZIONE QOL-ONE | |||||||||||||
Full Title: Lenalidomide for Myelodysplastic Syndromes: Efficacy, Safety, Cardiac Changes, and Quality of Life (QoL-ESC RevMDS) | |||||||||||||
Medical condition: Low or Intermediate-1 IPSS risk MDS with del(5q)as a single or combined cytogenetic abnormality and with anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003596-30 | Sponsor Protocol Number: MEDI4736-MDS-001 | Start Date*: 2016-05-23 | ||||||||||||||||
Sponsor Name:Celgene International II Sàrl | ||||||||||||||||||
Full Title: A Randomized Multicenter, Open-label, Phase 2 Study Evaluating the Efficacy and Safety of Azacitidine Subcutaneous in Combination With Durvalumab (MEDI4736) in Previously Untreated Subjects with Hi... | ||||||||||||||||||
Medical condition: Myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) PT (Completed) ES (Ongoing) AT (Completed) DE (Completed) BE (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003190-34 | Sponsor Protocol Number: ACE-536-MDS-002 | Start Date*: 2019-01-02 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 3, Open -label, Randomized Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) versus Epoetin Alfa for the Treatment of Anemia Due to IPSS-R Very Low, Low or Intermediate Ris... | |||||||||||||
Medical condition: Myelodysplastic syndrome (MDS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) LT (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) HU (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004685-32 | Sponsor Protocol Number: P02978 | Start Date*: 2005-08-22 |
Sponsor Name:Schering-Plough Research Institute | ||
Full Title: A Pivotal Randomized Study of Lonafarnib (SCH66336) Versus Placebo in the Treatment of Subjects With Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML) Who Are Platelet Transf... | ||
Medical condition: Platelet Transfusion Dependence in Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML) according to FAB criteria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) GR (Completed) AT (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-004884-20 | Sponsor Protocol Number: BRD 08/7-J | Start Date*: 2008-12-15 | |||||||||||||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||||||||||||
Full Title: Protocole Clinique de Phase II multicentrique non randomisé évaluant l’efficacité, la tolérance et la toxicité d’un conditionnement à intensité réduite combinant Clofarabine (Evoltra) + Busulfan IV... | |||||||||||||||||||||||
Medical condition: LAL Leucémie Aiguë lymphoblastique LAM Leucémie Aiguë Myéloblastique MDS Syndrome MyéloDysplasique | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003344-74 | Sponsor Protocol Number: HOVON116 | Start Date*: 2013-11-12 | ||||||||||||||||
Sponsor Name:HOVON Foundation | ||||||||||||||||||
Full Title: A phase I/II feasibility study of panoninostat alone and the combination of panobinostat and decitabine prior to donor lymphocyte infusion in recipients of allogeneic stem cell transplantation with... | ||||||||||||||||||
Medical condition: (very) poor risk AML or RAEB with IPSS ≥ 1.5 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002782-35 | Sponsor Protocol Number: A18-15331 | Start Date*: 2019-09-19 | |||||||||||
Sponsor Name:Aprea Therapeutics AB | |||||||||||||
Full Title: A Phase III Multicenter, Randomized, Open Label Study of APR-246 in Combination with Azacitidine Versus Azacitidine Alone for the Treatment of TP53 Mutant Myelodysplastic Syndromes | |||||||||||||
Medical condition: Myelodysplastic Syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000717-20 | Sponsor Protocol Number: CD-TCR-002 | Start Date*: 2019-10-09 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Medigene AG | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Long-Term Follow-Up Clinical Trial of Subjects Treated with PRAME TCR modified T cells, MDG1011 | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: High Risk Myeloid and Lymphoid Neopolasms | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023436-16 | Sponsor Protocol Number: HOVON 107 | Start Date*: 2011-05-31 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: The feasibility and efficacy of subcutaneous and intravenous Plerixafor for mobilization of peripheral blood stem cells in allogeneic HLA–identical sibling donors: a randomized phase II study. | |||||||||||||||||||||||
Medical condition: stem cell mobilization | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) DE (Restarted) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002915-93 | Sponsor Protocol Number: ACE-536-LTFU-001 | Start Date*: 2019-06-26 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Celgene Corporation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase 3B, open-label, single-arm, rollover study to evaluate long-term safety in subjects who have participated in other Luspatercept (ACE-536) clinical trials. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prior participation on a clinical trial of luspatercept (ACE-536) in protocols eligible for participation in this study ACE-536-LTFU-001 with the following medical conditions: - myelodysplastic syn... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) BE (Completed) BG (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004461-41 | Sponsor Protocol Number: CR-AIR-007 | Start Date*: 2013-06-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of ATIR, donor T-lymphocytes depleted ex vivo of host alloreactive T-cells, in patients with a hematologic malignan... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with a hematologic malignancy (AML, ALL, or MDS) who are eligible for a haploidentical HSCT | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006895-17 | Sponsor Protocol Number: MOLIVO-1 | Start Date*: 2022-12-02 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: Phase Ia/IIb study of PHD inhibitor molidustat in combination with IDH1 inhibitor ivosidenib in IDH1-mutated relapsed/refractory AML or MDS/AML patients | |||||||||||||
Medical condition: Adult patients with relapsed or refractory IDH1-mutated AML or relapsed/refractory MSD/AML with 10-19% bone marrow blasts at initial diagnosis and at screening (ECOG 0-2) after at least one prior l... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002471-34 | Sponsor Protocol Number: AZA-MDS-003 | Start Date*: 2012-11-23 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind Study to Compare the Efficacy and Safety of Oral Azacitidine Plus Best Supportive Care Versus Placebo Plus Best Supportive Care in Subjects With Red... | |||||||||||||
Medical condition: Subjects with Red Blood Cell Transfusion-Dependent Anemia and Thrombocytopenia due to IPSS Lower-Risk Myelodysplastic Syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NO (Completed) SE (Completed) ES (Ongoing) CZ (Completed) PT (Completed) LT (Completed) IT (Completed) NL (Completed) GB (GB - no longer in EU/EEA) DE (Completed) FI (Completed) DK (Completed) FR (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003576-40 | Sponsor Protocol Number: 74494550MDS2001 | Start Date*: 2020-04-24 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International N.V. | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Open-label Study of Cusatuzumab in Combination with Azacitidine Compared with Azacitidine Alone in Patients with Higher-risk Myelodysplastic Syndrome (MDS) or Chronic Myelomo... | ||||||||||||||||||
Medical condition: Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) ES (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000246-13 | Sponsor Protocol Number: GFM-REV-2006-02 | Start Date*: 2007-04-17 |
Sponsor Name:Groupe Français des myélodysplasies | ||
Full Title: 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] | ||
Medical condition: Myelodysplastic syndrome (MDS) is a clonal disease of the bone marrow stem cells. The disease is frequent/asociated with cytopenia and/or blastosis. an evolution to an acute leukemia is not frequen... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002821-20 | Sponsor Protocol Number: CR-AIR-008 | Start Date*: 2015-10-01 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of a two-dose regimen of ATIR101, a T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreacti... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with a hematologic malignancy (AML, ALL, or MDS) who are eligible for a haploidentical HSCT | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) PT (Completed) HR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003943-55 | Sponsor Protocol Number: MDS0706 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Clinical and biological effects of 5-Azacitidine five days/monthly schedule in symptomatic low-risk myelodysplastic syndromes (MDSs) | |||||||||||||
Medical condition: Adlut patients with low risk MDS (IPPS 0-1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003285-12 | Sponsor Protocol Number: BGB-11417-103 | Start Date*: 2022-05-17 |
Sponsor Name:BeiGene, Ltd. | ||
Full Title: A Phase 1b/2, Open-Label, Dose Finding, and Expansion Study of the Bcl-2 Inhibitor BGB-11417 in Patients With Myeloid Malignancies | ||
Medical condition: Myeloid malignancies (acute myeloid leukemia [AML], myelodysplastic syndromes [MDS], and myelodysplastic syndrome/myeloproliferative neoplasms [MDS/MPN]) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) ES (Ongoing) | ||
Trial results: (No results available) |
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