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Study identifier: NCT07204392 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Unveiling the Germline Predisposition to Myeloproliferative Neoplasms

Condition: Myeloproliferative Disease · Germline Mutation  ·  Sponsor: Fondazione IRCCS Policlinico San Matteo di Pavia

PhaseN/A
Planned participants313
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The classic Ph-negative myeloproliferative neoplasms (MPN) are a group of clonal hematopoietic disorders caused by a dysregulated JAK/STAT signal transduction because of acquired somatic mutations of JAK2, CALR or MPL genes. They are sporadic diseases but there are several lines of evidence that support the role of germline factors in the pathogenesis of MPN: the existence of familial clustering, the presence of more than one clone in some patients, the known existence of common polymorphisms that cause predisposition to MPN. In this study, we would like to define the germline predisposition to MPN.

This description comes directly from the study's public registry record.

Talk to the study team

Elisa Rumi  ·  0382-503084  ·  e.rumi@smatteo.pv.it

Always discuss trial participation with your own doctor first.

Locations (1)

Fondazione IRCCS Policlinico San MatteoPavia, Lombardy, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT07204392