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This study examines autoantibodies against type I interferon in patients with Ph-negative myeloproliferative neoplasms. People diagnosed with PV, ET, prePMF, overt PMF or MPN-U according to the 2016 WHO criteria who can provide a blood sample may take part. The study does not use a clinical phase and is active but not currently recruiting participants.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * A diagnosis of PV, ET, prePMF, overt PMF or MPN-U according to 2016 WHO criteria * Characterization of the MPN driver mutation performed at any moment before enrolment * A peripheral blood (PB) sample collected at the enrolment visit suitable for plasma extraction and functional evaluation of anti-cytokine auto-Abs Exclusion Criteria: * None