- Trials with a EudraCT protocol (77)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
77 result(s) found for: Decitabine.
Displaying page 1 of 4.
| EudraCT Number: 2015-004896-60 | Sponsor Protocol Number: LUMC2015-02 | Start Date*: 2015-11-26 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Decitabine-cytarabine chemotherapy in elderly AML and high risk MDS patients (> 65 years) with high early mortality risk | ||
| Medical condition: Acute myeloid leukemia and high risk myelodysplasia | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001060-38 | Sponsor Protocol Number: DECO | Start Date*: 2013-05-28 |
| Sponsor Name:Academic Medical center | ||
| Full Title: Pre-operative Decitabine in colon cancer: a proof of principal study | ||
| Medical condition: colon cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002324-41 | Sponsor Protocol Number: PH2/051 | Start Date*: 2006-11-30 | |||||||||||
| Sponsor Name:Cancer Research UK | |||||||||||||
| Full Title: A Cancer Research UK Randomised Multicentre Phase II Trial of the DNA-hypomethylating Agent, 5-Aza-2'-deoxycytidine(Decitabine) given intravenously in Combination with Carboplatin, versus Carboplat... | |||||||||||||
| Medical condition: Progressive, advanced ovarian cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| 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: 2015-001611-12 | Sponsor Protocol Number: 56022473AML2002 | Start Date*: 2015-07-03 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized Phase 2/3 Study of DACOGEN® (Decitabine) Plus JNJ-56022473 (Anti-CD123) Versus DACOGEN (Decitabine) Alone in Patients with AML who are not Candidates for Intensive Chemotherapy | |||||||||||||
| Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) SE (Completed) PL (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003586-34 | Sponsor Protocol Number: CYC682-12 | Start Date*: 2014-02-13 | |||||||||||
| Sponsor Name:Cyclacel Limited | |||||||||||||
| Full Title: A Phase III Randomized Study of Oral Sapacitabine in Elderly Patients with Newly Diagnosed Acute Myeloid Leukemia | |||||||||||||
| Medical condition: Acute myeloid leukemia (AML) is a cancer of the myeloid line of blood cells, characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with th... | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) DE (Completed) IT (Completed) GB (Completed) AT (Completed) IE (Completed) HU (Completed) ES (Completed) PL (Completed) FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) ES (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-002892-30 | Sponsor Protocol Number: 1315.2 | Start Date*: 2016-04-14 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: An open-label, Phase I/II trial to determine the maximum tolerated dose and investigate safety, pharmacokinetics and efficacy of BI 836858 in combination with decitabine in patients with acute myel... | |||||||||||||
| Medical condition: patients with acute myeloid leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003485-39 | Sponsor Protocol Number: NN7533-4470 | Start Date*: 2022-07-19 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A multicentre trial evaluating the efficacy and safety of oral decitabine-tetrahydrouridine (NDec) in patients with sickle cell disease | |||||||||||||
| Medical condition: Sickle cell disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001233-89 | Sponsor Protocol Number: SGI-110-04 | Start Date*: 2015-05-15 | |||||||||||
| Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Open-label, Randomized Study of SGI-110 versus Treatment Choice (TC) in Adults with Previously Untreated Acute Myeloid Leukemia (AML) Who Are Not Considered Candidates for I... | |||||||||||||
| Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) SE (Completed) BE (Completed) HU (Completed) DE (Completed) GB (Completed) NL (Completed) FI (Completed) CZ (Completed) AT (Completed) ES (Completed) PL (Completed) FR (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019755-21 | Sponsor Protocol Number: 04-21 | Start Date*: 2011-12-22 | |||||||||||
| Sponsor Name:Onconova Therapeutics Inc. | |||||||||||||
| Full Title: A Phase III, Multi-Center, Randomized, Controlled Study to Assess the Efficacy and Safety of ON 01910.Na Administered as a 72-Hour Continuous Intravenous Infusion Every Other Week in Myelodysplasti... | |||||||||||||
| Medical condition: Myelodysplastic syndrome with excess blasts | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Ongoing) IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000098-38 | Sponsor Protocol Number: GFM-SGI-110 | Start Date*: 2014-03-27 | |||||||||||
| Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | |||||||||||||
| Full Title: 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... | |||||||||||||
| Medical condition: Myelodysplastic syndrome high and Int-2, acute myeloid leukemia ≤ 30% marrow blasts and chronic monocytic leukemia (CMML) type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001486-27 | Sponsor Protocol Number: 1301-LG | Start Date*: 2015-05-29 | |||||||||||||||||||||||||||||||
| Sponsor Name:European Orgainzation for the Research and Treatment of Cancer (EORTC) | |||||||||||||||||||||||||||||||||
| Full Title: 10-day decitabine versus conventional chemotherapy (“3+7”) followed by allografting in AML patients ≥ 60 years: a randomized phase III study of the EORTC Leukemia Group, CELG, GIMEMA and German MDS... | |||||||||||||||||||||||||||||||||
| Medical condition: Acute Myeloid Leukaemia (AML) in elderly population (equal or older than 60 years). | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) LT (Completed) SK (Completed) BG (Completed) NL (Completed) IT (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-000047-31 | Sponsor Protocol Number: HOVON155 | Start Date*: 2019-09-30 | ||||||||||||||||
| Sponsor Name:HOVON Foundation | ||||||||||||||||||
| Full Title: A randomized phase II multicenter study to assess the tolerability and efficacy of the addition of midostaurin to 10-day decitabine in UNFIT (i.e. HCT-CI ≥ 3) adult AML and high risk myelodysplasia... | ||||||||||||||||||
| Medical condition: Acute Meyloid Leukemia and high risk myelodysplastic syndromes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-002675-29 | Sponsor Protocol Number: CC-486-MDS-006 | Start Date*: 2015-06-19 | |||||||||||
| Sponsor Name:Celgene Corporation | |||||||||||||
| Full Title: A Phase 2, International, Multicenter, Single-arm, Open-label Study to Evaluate the Efficacy and Safety of CC-486 (oral azacitidine) in Subjects With Myelodysplastic Syndromes Who Fail to Achieve a... | |||||||||||||
| Medical condition: Myelodysplastic syndrome (MDS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002632-23 | Sponsor Protocol Number: IFO21_02 | Start Date*: 2021-12-22 | |||||||||||
| Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
| Full Title: A proof-of-concept, biomarker-driven, phase-II clinical trial to explore the activity of decitabine repurposing against advanced, refractory, KRAS-dependent pancreatic ductal adenocarcinoma (PDAC):... | |||||||||||||
| Medical condition: Advanced (locally advanced or metastatic), pre-treated PDAC patients, progressing after at least one and no more than two lines of systemic therapy, whose tumors express a KRAS-dependency signature. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004772-18 | Sponsor Protocol Number: ASTX727-07 | Start Date*: 2022-05-30 | |||||||||||
| Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Single-Arm, Open-Label Pharmacokinetic, Safety, and Efficacy Study of ASTX727 in Combination with Venetoclax in Adult Patients with Acute Myeloid Leukemia | |||||||||||||
| Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Temporarily Halted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003482-28 | Sponsor Protocol Number: SGN33A-005 | Start Date*: 2016-07-14 | |||||||||||
| Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
| Full Title: A randomized, double-blind phase 3 study of vadastuximab talirine (SGN-CD33A) versus placebo in combination with azacitidine or decitabine in the treatment of older patients with newly diagnosed ac... | |||||||||||||
| Medical condition: Acute myeloid leukemia (AML) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) HU (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) BE (Completed) AT (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| 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: 2015-002855-85 | Sponsor Protocol Number: HO135 | Start Date*: 2016-03-18 | ||||||||||||||||
| Sponsor Name:HOVON Foundation | ||||||||||||||||||
| Full Title: A randomized phase II multicenter study to assess the tolerability and efficacy of the addition of ibrutinib to 10-day decitabine in UNFIT (i.e. HCT-CI ≥ 3) AML and high risk myelodysplasia (MDS) (... | ||||||||||||||||||
| Medical condition: Acute Meyloid Leukemia and High Risk Myelodysplastic syndromes | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) BE (Completed) LT (Prohibited by CA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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