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The purpose of the RELIEF study is to compare symptoms in polycythemia vera (PV) subjects treated with ruxolitinib versus subjects treated with hydroxyurea (HU) as measured by the percent of subjects ...
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Lead Sponsor
Incyte Corporation
NCT07357727 · Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (PPV-MF), and more
NCT06976918 · Primary Myelofibrosis, Secondary Myelofibrosis, and more
NCT06343805 · Primary Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis, and more
NCT05123365 · Myeloproliferative Neoplasm, MPN, and more
NCT06327100 · Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, and more
Scottsdale, Arizona
Fayetteville, Arkansas
Burbank, California
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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