MPNdpoint: Long-term Look at Philadelphia-negative Myeloproliferative Neoplasms
Official title: MPNdpoint. Single-center, Retrospective, Prospective Study of the Outcome of Patients With Philadelphia-negative Chronic Myeloproliferative Neoplasms
Run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · NCT07863466 · Data updated 2026-11-12
This study tests how outcomes differ for patients 16 and older with polycythemia vera, essential thrombocythemia, or myelofibrosis by collecting and analyzing clinical and treatment data.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 16 Years and up |
| Sex | All |
| Enrollment | 1190 (estimated) |
| Sponsor | Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico Academic / other |
| Locations | 1 site (Milan) |
| Status | Recruiting |
| Started | February 17, 2025 |
| Main results expected | June 2044 |
| Study ends | June 2044 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07863466 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients aged 16 or older with polycythemia vera, essential thrombocythemia, prefibrotic or overt primary myelofibrosis, or secondary myelofibrosis, with at least 6 months of follow-up.
✕Probably not a fit
Patients with diagnoses outside these MPN subtypes or with less than 6 months of follow-up may not benefit from the findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational study conducted at a single center to collect and review clinical, biological, and treatment information on patients with Philadelphia-negative myeloproliferative neoplasms. It includes both prefibrotic and overt primary myelofibrosis, secondary myelofibrosis, polycythemia vera, and essential thrombocythemia, aiming to build a database for better understanding of these diseases. The project retrospectively and prospectively aggregates data to examine outcomes and trends over time. Eligible participants are 16 years or older with these diagnoses and at least 6 months of follow-up. No interventional treatment is prescribed by the study protocol; data collection and analysis are the primary activities.
Why it matters
Potential benefit: If successful, the study could clarify real-world outcomes and help guide future research and care strategies for Philadelphia-negative MPNs.
How similar studies have gone: Previous work in similar registries and observational datasets has shown value in understanding MPN outcomes, though this exact centralized database approach is still being established.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients 16 years of age and older * Patients diagnosed with polycythemia vera, essential thrombocythemia, prefibrotic and overt primary myelofibrosis, secondary myelofibrosis (Arber et al, Blood 2022 or earlier but reclassified classifications) Exclusion Criteria: * Patients with diagnosis other than polycythemia vera, essential thrombocythemia, prefibrotic and overt primary myelofibrosis, secondary myelofibrosis * Follow up of less than 6 months
Where it's running
-
Ospedale Maggiore Policlinico
Milan, Italy Recruiting
Study contacts
- Study coordinator: Barbara Mora, MD
- Email: barbara.mora@policlinico.mi.it
- Phone: +39 0255033345
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.