- Trials with a EudraCT protocol (90)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
90 result(s) found for: Polycythemia vera.
Displaying page 1 of 5.
EudraCT Number: 2021-004732-29 | Sponsor Protocol Number: PTG-300-11 | Start Date*: 2022-06-21 | ||||||||||||||||
Sponsor Name:Protagonist Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Study of the Hepcidin Mimetic Rusfertide (PTG-300) in Patients with Polycythemia Vera | ||||||||||||||||||
Medical condition: Polycythemia Vera | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) HU (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) PT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004717-25 | Sponsor Protocol Number: Low-PV | Start Date*: 2016-07-08 | |||||||||||
Sponsor Name:FONDAZIONE PER LA RICERCA OSPEDALE MAGGIORE DI BERGAMO - FROM | |||||||||||||
Full Title: The benefit/risk profile of pegylated proline-Interferon alpha-2b (AOP2014) added to the best available strategy based on phlebotomies in low-risk patients with Polycythemia Vera (PV). The Low-PV r... | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018768-18 | Sponsor Protocol Number: P11012010 | Start Date*: 2010-07-02 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: An open-label, prospective, multicentre, phase I/II dose escalation study to determine the maximum tolerated dose and to assess the safety and efficacy of P1101, PEG-Proline-Interferon alpha-2b for... | |||||||||||||
Medical condition: Diagnosis for Polycythemia Vera as per the WHO or PVSG. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001908-11 | Sponsor Protocol Number: RG_16-148 | Start Date*: 2022-09-12 | |||||||||||
Sponsor Name:UNIVERSITY OF BIRMINGHAM | |||||||||||||
Full Title: A phase III, randomised, open-label, Multicenter International Trial comparing ruxolitinib with either HydRoxycarbamIDe or interferon Alpha as first line ThErapyfor high risk polycythemia vera | |||||||||||||
Medical condition: Myeloproliferative neoplasm (MPN), specifically Polycythaemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007801-63 | Sponsor Protocol Number: 1113/08 | Start Date*: 2010-01-07 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: International Study using Clopidogrel and Aspirin for the treatment of Polycythemia Vera. | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001356-31 | Sponsor Protocol Number: PEN-PV | Start Date*: 2015-05-20 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: An open-label, single arm, Phase III study to assess the self-administration of AOP2014 using a pre-filled pen, developed for the treatment of Polycythemia Vera patients | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) AT (Completed) CZ (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003704-40 | Sponsor Protocol Number: ISIS702843-CS4 | Start Date*: 2023-02-27 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2a, Randomized, Open-Label Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ISIS 702843 Administered to Patients with Phlebotomy Dependent Pol... | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2007-006647-45 | Sponsor Protocol Number: D1060C00001 | Start Date*: 2009-05-14 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Phase I/II, Open Label Multi-Centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the JAK2 inhibitor AZD1480 Administered Orally to Patients with Primary ... | ||||||||||||||||||
Medical condition: Myeloproliferative disorders including Primary Myelofibrosis (PMF) and Post-Polycythaemia Vera/Essential Thrombocythaemia Myelofibrosis (Post-PV/ET MF). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001309-42 | Sponsor Protocol Number: CINC424B2001X | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, multi-center, Expanded Treatment Protocol (ETP) of ruxolitinib in patients with Polycythemia Vera who are Hydroxyurea resistant or intolerant and for whom no treatment alternatives a... | |||||||||||||
Medical condition: hydroxyurea resistant or intolerant patients with polycythemia vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) NO (Completed) SK (Completed) PT (Completed) SE (Completed) BE (Completed) BG (Completed) | |||||||||||||
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: 2010-020807-57 | Sponsor Protocol Number: CINC424B2301 | Start Date*: 2011-02-08 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Randomized, open label, multicenter phase III study of Efficacy and Safety in Polycythemia vera subjects who are resistant to or intolerant of hydroxyurea: JAK iNhibitor INC424 tablets verSus bEst ... | |||||||||||||
Medical condition: Polycythemia vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) GB (Completed) IT (Completed) NL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003583-31 | Sponsor Protocol Number: CINC424B2401 | Start Date*: 2014-02-17 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Randomized, open label, multicenter phase IIIb study evaluating the efficacy and safety of ruxolitinib versus best available therapy in patients with polycythemia vera who are hydroxyurea resistant... | |||||||||||||
Medical condition: Polycythemia vera resistant or intolerant to hydroxyurea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) HU (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000860-27 | Sponsor Protocol Number: DSC/12/2357/45 | Start Date*: 2013-06-20 | |||||||||||
Sponsor Name:ITALFARMACO S.p.A | |||||||||||||
Full Title: A two-part study to assess the safety and preliminary efficacy of Givinostat in patients with JAK2V617F positive Polycythemia Vera | |||||||||||||
Medical condition: JAK2V617F positive Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FR (Completed) DE (Completed) GB (Completed) PL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 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) |
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