- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Myeloid Tissue.
Displaying page 1 of 3.
EudraCT Number: 2007-000597-22 | Sponsor Protocol Number: GIMEMACML0307 | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: The protein tyrosine kinase inhibitor nilotinib as first-line treatment of Ph+ chronic myeloid leucemia (CML) in early chronic phase: a Phase II exploratory, multicenter study | |||||||||||||
Medical condition: Ph+ CML in early chronic phase | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003087-45 | Sponsor Protocol Number: MYLOX-1 | Start Date*: 2021-04-22 | |||||||||||||||||||||
Sponsor Name:Galecto Biotech AB | |||||||||||||||||||||||
Full Title: An open-label, phase IIa study of the safety, tolerability, pharmacokinetics and pharmacodynamics of oral GB2064 (a LOXL2 inhibitor) in participants with myelofibrosis (The MYLOX-1 study). | |||||||||||||||||||||||
Medical condition: Primary (PMF) or secondary (SMF) myelofibrosis. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002847-14 | Sponsor Protocol Number: CU 106 | Start Date*: 2005-12-16 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: AML16; A National Cancer Research Institute Trial in Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndromes | |||||||||||||
Medical condition: Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003936-21 | Sponsor Protocol Number: AML1919 | Start Date*: 2020-04-09 | ||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||
Full Title: A Phase 3, prospective, randomized multi-center intervention trial of early intensification in AML patients bearing FLT3 mutations based on peripheral blast clearance. A MYNERVA-GIMEMA study. AMEL... | ||||||||||||||||||
Medical condition: Acute Myeloid Leukemia (LMA) with FLT3 mutation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000920-26 | Sponsor Protocol Number: KCP-330-008 | Start Date*: 2014-09-08 | |||||||||||
Sponsor Name:Karyopharm Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized, Open Label, Phase 2 Study of the Selective Inhibitor of Nuclear Export (SINE) Selinexor (KPT-330) versus Specified Physician’s Choice in Patients ≥ 60 Years Old with Relapsed/Refracto... | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) NL (Completed) GB (Completed) DK (Prematurely Ended) BE (Completed) HU (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003426-32 | Sponsor Protocol Number: DCOne-002 | Start Date*: 2017-12-11 | |||||||||||
Sponsor Name:DCprime bv | |||||||||||||
Full Title: AN INTERNATIONAL, MULTICENTRE, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TWO DIFFERENT VACCINATION REGIMENS OF IMMUNOTHERAPY WITH ALLOGENEIC DENDRITIC CELLS, DCP-001, IN PATIENTS WIT... | |||||||||||||
Medical condition: The medical condition investigated are patients with acute myeloid leukemia in complete remission with persistent minimal residual disease and as such are at high risk of relapse. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) DE (Ongoing) NO (Ongoing) SE (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001718-80 | Sponsor Protocol Number: PRM-151G-101 | Start Date*: 2016-02-18 | |||||||||||||||||||||
Sponsor Name:Promedior, Inc | |||||||||||||||||||||||
Full Title: A Phase 2, Prospective Study Of PRM-151 In Subjects With Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (post-PV MF), Or Post-Essential Thrombocythemia MF (post-ET MF) | |||||||||||||||||||||||
Medical condition: Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (post-PV MF), Or Post-Essential Thrombocythemia MF (post-ET MF) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) FR (Completed) DE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000392-33 | Sponsor Protocol Number: AML1718 | Start Date*: 2018-08-29 | |||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | |||||||||||||
Full Title: A Safety Run-in and phase II, open-label, multicentre, study investigating safety, tolerability and effectiveness of Venetoclax add in combination at Fludarabine, Cytarabine and Idarubicine in ind... | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005010-19 | Sponsor Protocol Number: MPD-RC114 | Start Date*: 2014-11-25 | |||||||||||
Sponsor Name:Consorzio Mario Negri Sud | |||||||||||||
Full Title: Exploring the Potential of Dual Kinase JAK 1/2 Inhibitor Ruxolitinib (INC424) with Reduced Intensity Allogeneic Hematopoietic Cell Transplantation in Patients with Myelofibrosis | |||||||||||||
Medical condition: Primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PPV-MF) and post-essential thrombocythemia myelofibrosis (PET-MF), collectively known as myelofibrosis (MF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003811-23 | Sponsor Protocol Number: IMG-7289-CTP-102 | Start Date*: 2019-12-11 | |||||||||||||||||||||
Sponsor Name:Imago BioSciences, Inc. | |||||||||||||||||||||||
Full Title: A Multi-Center, Open Label Study to Assess the Safety, Steady State Pharmacokinetics and Pharmacodynamics of IMG-7289 in Patients with Myelofibrosis | |||||||||||||||||||||||
Medical condition: Myelofibrosis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) IT (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004839-23 | Sponsor Protocol Number: CA-4948-102 | Start Date*: 2023-02-09 | ||||||||||||||||
Sponsor Name:Curis, Inc | ||||||||||||||||||
Full Title: A Phase 1/2a, Open-Label Dose Escalation and Cohort Expansion Study of Orally Administered CA-4948(IRAK4i) as a Monotherapy in patients with Acute Myelogenous Leukemia or Myelodysplastic Syndrome a... | ||||||||||||||||||
Medical condition: Acute Myelogenous Leukemia (AML) or high risk Myelodysplastic Syndrome (MDS). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) PL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004295-18 | Sponsor Protocol Number: 080487 | Start Date*: 2019-12-13 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Fibrinogen and platelets in patients with acute myeloid leukaemia and thrombocytopenia | |||||||||||||
Medical condition: Bleeding i patients with acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001560-14 | Sponsor Protocol Number: FJD-RA-TOF-60418809 | Start Date*: 2021-08-13 |
Sponsor Name:FUNDACION JIMENEZ DIAZ HEALTH RESEARCH INSTITUTE | ||
Full Title: Single-center, open-label, uncontrolled clinical trial to evaluate the association between the expression of the JAK / STAT pathway and the response to tofacitinib in patients with refractory rheum... | ||
Medical condition: Refractory rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000168-53 | Sponsor Protocol Number: EP0042-101 | Start Date*: 2020-07-29 | |||||||||||||||||||||
Sponsor Name:Ellipses Pharma Limited | |||||||||||||||||||||||
Full Title: A Modular, Multipart, Multi-arm, Open-label, Phase I/IIa Study to Evaluate the Safety and Tolerability of EP0042 Alone and in Combination with Anti-cancer Treatments in Patients with Advanced Malig... | |||||||||||||||||||||||
Medical condition: Acute myeloid leukaemia (AML), Chronic myelomonocytic leukaemia (CMML) and Myelodysplastic syndrome (MDS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000200-38 | Sponsor Protocol Number: VitDM3BH | Start Date*: 2021-06-13 |
Sponsor Name:University Clinic of Dentistry, Medical University of Vienna | ||
Full Title: THE IMPACT OF VITAMIN D3 HIGH DOSES SUPPLEMENTATTION ON SOFT TISSUE WOUND-HEALING AFTER MANDIBULAR THIRD MOLAR (M3) REMOVAL: A PILOT STUDY | ||
Medical condition: Vitamin D insufficiency undergoing tooth extraction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023757-11 | Sponsor Protocol Number: myDC/pDCinstageIIImelanoma | Start Date*: 2014-11-06 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Myeloid and plasmacytoid blood dendritic cells for immunotherapy of stage III melanoma patients scheduled for radical lymph node dissection | ||
Medical condition: melanoma patients with regional lymph node metastases (stage III) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003418-41 | Sponsor Protocol Number: NAV3-32 | Start Date*: 2020-05-18 | |||||||||||
Sponsor Name:Navidea Biopharmaceuticals Ltd | |||||||||||||
Full Title: A Comparison of Tc 99m Tilmanocept Quantitative Imaging with Immunohistochemical (IHC) Analysis of CD206 Expression in Synovial Tissue from Subjects Clinically Diagnosed with Rheumatoid Arthritis (RA) | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001522-41 | Sponsor Protocol Number: PACT2014-001 | Start Date*: 2016-02-08 | ||||||||||||||||
Sponsor Name:University Hospital Wuerzburg | ||||||||||||||||||
Full Title: Prophylactic application of donor-derived central memory T lymphocytes (TCM) after allogeneic HSCT to prevent infectious complications | ||||||||||||||||||
Medical condition: patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) after T cell depleted allo-SCT | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002730-21 | Sponsor Protocol Number: SPON1227-13 | Start Date*: 2013-11-25 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A Trial for Older Patients with Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
Medical condition: Acute Myeloid Leukaemia High Risk Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003280-35 | Sponsor Protocol Number: 2017BN003 | Start Date*: 2017-11-22 | |||||||||||
Sponsor Name:UZ Brussel | |||||||||||||
Full Title: AMENDMENT TITLE: Phase I clinical trial on intratumoral administration of autologous CD1c (BDCA-1)+ / CD141 (BDCA-3)+ myeloid dendritic cells plus ipilimumab and AS01 in combination with intravenou... | |||||||||||||
Medical condition: Patients with injectable metastases from histologically confirmed solid tumors who have failed standard-of-care life prolonging therapeutic options will be invited to participate in this clinical t... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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