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NCT07204392

Unveiling the Germline Predisposition to Myeloproliferative Neoplasms

Recruiting now Last updated 2 October 2025
What this trial tests

trial in Myeloproliferative Disease in 313 participants. Currently enrolling.

Timeline
27 June 2022
Primary endpoint
31 December 2030
31 December 2030

Quick facts

Lead sponsorFondazione IRCCS Policlinico San Matteo di Pavia
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment313
Start date27 June 2022
Primary completion31 December 2030
Estimated completion31 December 2030
Sites1 location across Italy

Conditions studied

Sponsor

Fondazione IRCCS Policlinico San Matteo di Pavia

Who can join

18 and older, any sex, with Myeloproliferative Disease or Germline Mutation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myeloproliferative Disease

Currently open trials in the same condition.

Other Fondazione IRCCS Policlinico San Matteo di Pavia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07204392.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing