- Trials with a EudraCT protocol (75)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
75 result(s) found for: Essential thrombocythemia.
Displaying page 1 of 4.
EudraCT Number: 2015-002798-39 | Sponsor Protocol Number: 2015050991 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:Anne-Mette Hvas | |||||||||||||
Full Title: Platelet Function and Treatment with ASA in patients with Essential Thrombocytosis | |||||||||||||
Medical condition: Essential thrombocytosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017095-24 | Sponsor Protocol Number: AOP13007 | Start Date*: 2010-02-17 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: A phase III, randomized, multicenter, subject- and sponsor-blinded, placebo controlled study to compare the efficacy and safety of “Anagrelide retard” versus placebo in “at risk” subjects with Esse... | |||||||||||||
Medical condition: male and female "at risk" subjects with Essential Thrombocythaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) SI (Completed) LT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004061-15 | Sponsor Protocol Number: SPD422-403 | Start Date*: 2005-07-07 | |||||||||||
Sponsor Name:Shire Pharmaceutical Development Ltd. | |||||||||||||
Full Title: A Phase IIIb, randomised, open label study to compare the safety, efficacy and tolerability of anagrelide hydrochloride versus hydroxyurea in high-risk essential thrombocythaemia patients. | |||||||||||||
Medical condition: Essential thrombocythaemia (ET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IE (Completed) ES (Completed) IT (Completed) SK (Completed) CZ (Completed) SI (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002885-30 | Sponsor Protocol Number: ARES | Start Date*: 2017-07-27 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Novel strategies of antithrombotic prophylaxis in patients with Essential Thrombocythemia (ET) at high risk of cardiovascular events: comparison of different dosing regimens of administration of l... | |||||||||||||
Medical condition: Essential thrombocytemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023076-10 | Sponsor Protocol Number: CP14B015 | Start Date*: 2011-02-28 | |||||||||||
Sponsor Name:Geron Corporation | |||||||||||||
Full Title: A Phase II Trial to Evaluate the Activity of Imetelstat (GRN163L) in Patients with Essential Thrombocythemia who Require Cytoreduction and Have Failed or Are Intolerant to Previous Therapy, or who ... | |||||||||||||
Medical condition: Essential thrombocythemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003410-41 | Sponsor Protocol Number: AOP18007 | Start Date*: 2014-01-13 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: A phase III randomized, multicenter, double-blind, active controlled study to compare the efficacy and safety of two different anagrelide formulations in patients with Essential Thrombocythemia (TE... | |||||||||||||
Medical condition: male or female patients with confirmed diagnosis of Essential Thrombocythemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) LT (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003659-13 | Sponsor Protocol Number: IMG-7289-CTP-201 | Start Date*: 2020-06-21 | |||||||||||
Sponsor Name:Imago BioSciences Inc. | |||||||||||||
Full Title: A Phase 2 Multi-Center, Open Label Study to Assess the Safety,Efficacy and Pharmacodynamics of IMG-7289 in Patients with Essential Thrombocythemia | |||||||||||||
Medical condition: Patients with essential thrombocythemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007335-99 | Sponsor Protocol Number: Tarceva-HH-2008 | Start Date*: 2009-08-24 | ||||||||||||||||
Sponsor Name:Herlev Hospital, Dept. of Haematology (L121) | ||||||||||||||||||
Full Title: A Phase II Study of Erlotinib in Patients with Polycythaemia Vera and Essential Thrombocythemia | ||||||||||||||||||
Medical condition: Polycythaemia Vera & Essential Thrombocythaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001406-42 | Sponsor Protocol Number: 30032016 | Start Date*: 2016-12-20 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Hæmatologisk Afdeling, Sjælland Sygehus, Roskilde | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Statin- and bisphosphonate treatment in patients with the Philadelphia-negative chronic myeloproliferative neoplasms - essential thrombocytosis, polycythemia vera and hypercellular myelofibrosis. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: The Philadelphia-negative chronic myeloproliferative neoplasms: Essential thrombocytosis, polycythemia vera and hypercellular myelofibrosis. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012784-34 | Sponsor Protocol Number: 384/09 | Start Date*: 2009-07-08 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: STUDY OF HYDROXYUREA MECHANISMS OF ACTION ON LEUKOCYTE ACTIVATION IN PATIENTS WITH CHRONIC MYELOPROLIFERATIVE SYNDROMES. | ||||||||||||||||||
Medical condition: MYELOPROLIFERATIVE SYNDROMES | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019500-23 | Sponsor Protocol Number: MPD-RC111 | Start Date*: 2012-02-15 | ||||||||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | ||||||||||||||||||
Full Title: Single Arm Salvage Therapy with Pegylated Interferon Alfa-2a for Patients with High Risk Polycythemia Vera or High Risk Essential Thrombocythemia who are Either Hydroxyurea Resistant or Intolerant ... | ||||||||||||||||||
Medical condition: High risk polycythemia vera and high risk essential thrombocythemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001382-28 | Sponsor Protocol Number: INCB 18424-256 | Start Date*: 2008-09-19 | ||||||||||||||||
Sponsor Name:Incyte Corporation | ||||||||||||||||||
Full Title: A Phase 2, open label, dose regimen ranging clinical study to determine the safety and efficacy of INCB018424 in patients with advanced polycythemia vera or essential thrombocythemia refractory ... | ||||||||||||||||||
Medical condition: advanced polycythemia vera or essential thrombocythemia refractory to hydroxyurea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005306-49 | Sponsor Protocol Number: MK-0683-092 | Start Date*: 2008-09-03 | |||||||||||||||||||||
Sponsor Name:Department of Haematology, Herlev Hospital, University of Copenhagen | |||||||||||||||||||||||
Full Title: A Phase II Study of Vorinostat in Patients with Polycythaemia Vera and Essential Thrombocythaemia | |||||||||||||||||||||||
Medical condition: patients with polycythaemia vera or essential thrombocythaemia or myelofibrosis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) SE (Completed) NL (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004105-11 | Sponsor Protocol Number: GS-US-354-0101 | Start Date*: 2014-07-04 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
Full Title: A Phase 2, Open-label, Randomized Study to Evaluate Safety and Efficacy of Momelotinib in Subjects with Polycythemia Vera or Essential Thrombocythemia | ||||||||||||||||||
Medical condition: subjects with either polycythemia vera (PV) or essential thrombocythemia (ET) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004652-15 | Sponsor Protocol Number: 29BRC20.0263 | Start Date*: 2021-06-08 | ||||||||||||||||||||||||||
Sponsor Name:CHRU de Brest | ||||||||||||||||||||||||||||
Full Title: AVAJAK: Apixaban/rivaroxaban Versus Aspirin for primary prevention of thrombo-embolic complications in JAK2V617F-positive myelo-proliferative neoplasms | ||||||||||||||||||||||||||||
Medical condition: Myelo-proliferative neoplasms including essential thrombocythemia, Polycythemia Vera, Prefibrotic myelofibrosis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005279-18 | Sponsor Protocol Number: RG_11-164 | Start Date*: 2012-02-08 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: A RandoMised study of best Available therapy versus JAK Inhibition in patients with high risk Polycythaemia Vera or Essential Thrombocythaemia who are resistant or intolerant to HydroxyCarbamide. | ||||||||||||||||||
Medical condition: Polycythaemia vera Essential Thrombocythaemia | ||||||||||||||||||
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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: 2010-019501-41 | Sponsor Protocol Number: MPD-RC112 | Start Date*: 2012-02-15 | ||||||||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | ||||||||||||||||||
Full Title: Randomized Trial of Pegylated Interferon Alfa-2a versus Hydroxyurea Therapy in the Treatment of High Risk Polycythemia Vera and High Risk Essential Thrombocythemia | ||||||||||||||||||
Medical condition: High Risk Polycythemia Vera or High Risk Essential Thrombocythemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) SE (Ongoing) GB (Completed) DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004476-36 | Sponsor Protocol Number: GS-US-352-1154 | Start Date*: 2014-12-11 | |||||||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||||||||||||
Full Title: Open-label Study to Assess the Long-term Safety and Efficacy of Momelotinib in Subjects with Primary Myelofibrosis, Post polycythemia Vera Myelofibrosis, Post essential Thrombocythemia Myelofibros... | |||||||||||||||||||||||
Medical condition: subjects with either primary myelofibrosis (PMF) or post polycythemia vera myelofibrosis or post essential thrombocythemia myelofibrosis (post-PV / ET MF) or polycythemia vera (PV) or essential thr... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000579-34 | Sponsor Protocol Number: 0610-02 | Start Date*: 2018-07-02 | ||||||||||||||||
Sponsor Name:Constellation Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2 Study of CPI-0610, a Small Molecule Inhibitor of BET Proteins: Phase 1 (Dose Escalation of CPI-0610 in Patients with Hematological Malignancies) and Phase 2 (Dose Expansion of CPI-0610 ... | ||||||||||||||||||
Medical condition: Myeloproliferative Neoplasms (Myelofibrosis and Essential Thrombocythemia) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) BE (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001012-56 | Sponsor Protocol Number: I3X-MC-JHTB | Start Date*: 2012-08-30 | |||||||||||||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||||||||||||
Full Title: A Phase 2 Study of LY2784544 in Patients with Myeloproliferative Neoplasms | |||||||||||||||||||||||
Medical condition: Myeloproliferative neoplasms (MPNs), myelofibrosis, essential thrombocythemia, and polycythemia vera | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) SE (Completed) AT (Trial now transitioned) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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