- Trials with a EudraCT protocol (136)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
136 result(s) found for: Chronic myelomonocytic leukemia.
Displaying page 1 of 7.
EudraCT Number: 2009-014561-77 | Sponsor Protocol Number: DECI-2009-AISSM06 | Start Date*: 2010-03-16 | ||||||||||||||||||||||||||
Sponsor Name:AISSM ONLUS | ||||||||||||||||||||||||||||
Full Title: Phase III multicentric open label study to assess the effectiveness of decitabine in the treatment of chronic myelomonocytic leukemia | ||||||||||||||||||||||||||||
Medical condition: patients with myelodisplastic syndrome | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017147-33 | Sponsor Protocol Number: AGMT_CMML1 | Start Date*: 2010-02-10 | |||||||||||
Sponsor Name:AGMT gemeinnützige GmbH | |||||||||||||
Full Title: A Phase I/II Study of Lenalidomide in Patients with Chronic Myelomonocytic Leukemia | |||||||||||||
Medical condition: Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002977-22 | Sponsor Protocol Number: 108/2004/U | Start Date*: 2004-09-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: A PHASE II STUDY OF VELCADE BORTEZOMIB - PS341 IN THE TREATMENT OF PATIENTS OVER 18 YEARS WITH Ph LEUKEMIA | |||||||||||||
Medical condition: patients over 18 years with Ph leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002007-35 | Sponsor Protocol Number: AVENHIR | Start Date*: 2023-03-02 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | |||||||||||||
Full Title: Phase II study with safety run-in of Azacitidine (AZA) combined with Venetoclax (VEN) in patients with higher-risk Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
Medical condition: Newly diagnosed, HMA-naïve, higher-risk (HR, defined as CPSS risk intermediate-2 or high) CMML patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002281-23 | Sponsor Protocol Number: Spon1345-14 | Start Date*: 2016-06-13 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A phase 2 study of the monocyte-targeted histone deacetylase inhibitor tefinostat (CHR-2845) in chronic myelomonocytic leukaemia (CMML) | |||||||||||||
Medical condition: Chronic myelomonocytic leukaemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000470-21 | Sponsor Protocol Number: JNJ-30979754 | Start Date*: 2008-08-04 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A Phase II study of Decitabine in patients with Chronic Myelomonocytic Leukemia | |||||||||||||
Medical condition: Chronic Myelomonocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010548-32 | Sponsor Protocol Number: CLBH589H2101 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A phase Ib/IIb, open-label, multi-center study of oral Panobinostat (LBH589) administered with 5-Azacitidine (Vidaza®) in adult patients with myelodysplastic syndromes (MDS), chronic myelomonocytic... | |||||||||||||||||||||||
Medical condition: Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), or acute myeloid leukemia (AML) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) SE (Prematurely Ended) AT (Prematurely Ended) ES (Completed) BE (Completed) GB (Prematurely Ended) HU (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006349-23 | Sponsor Protocol Number: HM08/8540 | Start Date*: 2009-04-28 | |||||||||||
Sponsor Name:The Leeds Teaching Hospitals NHS Trust | |||||||||||||
Full Title: CMML201: A phase 2 study of azacitidine in chronic myelomonocytic leukaemia (CMML) | |||||||||||||
Medical condition: Chronic Myelomonocytic Leukaemia (CMML): Patients with newly diagnosed or previously treated CMML-1 or CMML-2. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000346-30 | Sponsor Protocol Number: CINC424XDE04T | Start Date*: 2015-03-16 | ||||||||||||||||
Sponsor Name:Universität Leipzig | ||||||||||||||||||
Full Title: An open-label, multicenter study of INC424 monotherapy or in combination with azacitidine for patients with post-myeloproliferative disorders (MPD) – AML or with CMML | ||||||||||||||||||
Medical condition: Chronic Myelomonocytic Leukemia and secondary Acute myeloid leukemia | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003395-12 | Sponsor Protocol Number: ASTX727-02 | Start Date*: 2019-11-14 | |||||||||||||||||||||
Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||||||||||||
Full Title: A Phase 3, Randomized, Open-Label, Crossover Study of ASTX727 (Cedazuridine and Decitabine Fixed-Dose Combination) versus IV Decitabine in Subjects with Myelodysplastic Syndromes (MDS), Chronic Mye... | |||||||||||||||||||||||
Medical condition: Acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), and chronic myelomonocytic leukemia (CMML) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) AT (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000200-10 | Sponsor Protocol Number: GFM-DAC-CMML | Start Date*: 2014-08-12 | |||||||||||
Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | |||||||||||||
Full Title: A Randomized Phase III study of Decitabine (DAC) with or without Hydroxyurea (HY) versus HY in patients with advanced proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
Medical condition: Proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004370-10 | Sponsor Protocol Number: RUXO_LMMC-PRO_1401 | Start Date*: 2014-03-21 | |||||||||||
Sponsor Name:Grupo Español de Sindromes Mielodisplásicos (GESMD) | |||||||||||||
Full Title: A phase II study of ruxolitinib (INCB018424) to evaluate efficacy and safety in Patients with Proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
Medical condition: Proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001361-29 | Sponsor Protocol Number: CLWP 001 2008 | Start Date*: 2009-10-08 | |||||||||||
Sponsor Name:EBMT (European group for Blood and Marrow Transplantation) | |||||||||||||
Full Title: Phase II efficacy and safety study of Dasatinib in Patients with Chronic and Accelerated Phase Chronic Myeloid Leukaemia Relapsing after Allogeneic Blood or Bone Marrow Transplantation | |||||||||||||
Medical condition: chronic myeloid leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017098-40 | Sponsor Protocol Number: DEC-MDS | Start Date*: 2010-07-09 | |||||||||||||||||||||||||||||||
Sponsor Name:King's College London [...] | |||||||||||||||||||||||||||||||||
Full Title: Use of Decitabine in Myelodysplastic Syndrome (MDS) Following Azacitidine (AZA) Failure (DEC-MDS) | |||||||||||||||||||||||||||||||||
Medical condition: Myelodysplastic Syndromes Acute Myeloid Leukaemia Chronic Myelomonocytic Leukaemia | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001334-18 | Sponsor Protocol Number: CarPAs | Start Date*: 2020-09-10 | ||||||||||||||||
Sponsor Name:Associazione Italiana Pazienti Leucemia Mieloide Cronica (AIPLMC) | ||||||||||||||||||
Full Title: Cardiovascular assessment of Ponatinib as treatment option in chronic phase chronic myeloid leukemia after failure of Imatinib and Bosutinib (CarPAs) | ||||||||||||||||||
Medical condition: Chronic Myeloid Leukemia (CML) in Chronic Phase (CP) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000899-28 | Sponsor Protocol Number: CAMN107CNL08T | Start Date*: 2018-09-04 | |||||||||||||||||||||
Sponsor Name:Albert Schweitzer Hospital | |||||||||||||||||||||||
Full Title: Dipeptidylpeptidase IV (CD26) on Philadelphia-positive leukemic stem cells (LSC) as marker and novel therapeutic target in chronic myeloid leukemia (CML). | |||||||||||||||||||||||
Medical condition: Chronic myeloid leukemia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011483-11 | Sponsor Protocol Number: NMDSG08A | Start Date*: 2009-11-18 | ||||||||||||||||
Sponsor Name:NMDSG | ||||||||||||||||||
Full Title: Clinical and biological evaluation of azacitidine in transfusion-dependent patients with Low and intermediate-1 risk MDS, and low-risk CMML, who are either refractory to or not eligible for treatme... | ||||||||||||||||||
Medical condition: Low and intermediate-1 risk MDS, and low-risk CMML. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001381-14 | Sponsor Protocol Number: CSTI5710109E2 | Start Date*: 2005-08-02 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II study to determine the safety and the anti- leukemic effects of STI571 in adults patients with Philadelphia chromosome positive leukemia including acute lymphoblastic le... | |||||||||||||
Medical condition: Philadelphia chromosome positive leukemia including acute lymphoblastic leukemia, acute myeloid leukemia and accelerate phase myeloid leukemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003674-26 | Sponsor Protocol Number: MK0457-009 | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:MERCK SHARP DOHME | |||||||||||||
Full Title: A Phase I Dose Escalation of MK-0457 in Combination With Dasatinib in Patients With Refractory Chronic Myelogenous Leukemia and Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia. | |||||||||||||
Medical condition: Patients with Refractory Chronic Myelogenous Leukemia and Philadelphia Chromosome-Positive Acute Lymphoblastic. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004422-30 | Sponsor Protocol Number: CMBG453B12206B | Start Date*: 2022-07-21 | ||||||||||||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||||||||||||
Full Title: An open-label, multicenter, roll-over study for patients who have completed a prior Novartis-sponsored sabatolimab (MBG453) study and are judged by the investigator to benefit from continued treatm... | ||||||||||||||||||||||||||||
Medical condition: intermediate, high or very high risk MDS in adult patients chronic Myelomonocytic Leukemia - 2 (CMML-2) Acute Myeloid Leukemia (AML) in adult patients unfit for chemotherapy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) BE (Completed) CZ (Trial now transitioned) DE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) FR (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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