MPN PROGRESSion Registry: Understanding Myeloproliferative Neoplasms
This is an observational study, not a treatment trial, designed to better understand myeloproliferative neoplasms (MPNs). These are rare, chronic blood cancers like polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (MF). Researchers will track your symptoms, treatments, and how your disease progresses over time. The goal is to gather real-world information from 5,000 participants to help improve care and research for people with MPNs. You may be eligible if you are an adult aged 18 or older with a confirmed MPN diagnosis, even if you've had a stem cell or bone marrow transplant.
- Study design
- This is an observational study aiming to enroll 5,000 participants. It is not testing a new intervention but rather collecting information over time.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed continuously from enrollment for a minimum of 5 years, with potential follow-up extending beyond 10 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
MPN PROGRESSion Registry: Observational Study Tracking Symptoms, Treatments, and Disease Progression in People With Myeloproliferative Neoplasms (MPNs)
At a glance
Conditions
Where it's being run
2 sites across 2 statesStudy leadership
- Raajit Rampal, MD, PhD · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center
Who to contact
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Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Time to Disease ProgressionAssessed continuously from enrollment over a minimum of 5 years per participant, with extended follow-up beyond 10 years for participants who remain active in the registry.
Time from enrollment to the first documented disease progression event, defined as transformation between MPN subtypes (for example, essential thrombocythemia or polycythemia vera to myelofibrosis), development of accelerated-phase MPN (MPN-AP), progression to blast phase (MPN-BP), or meeting updated World Health Organization (WHO) or International Working Group for Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) criteria for disease progression. This outcome measures the rate and timing of disease evolution over time and evaluates associations with treatments, exposures, and clinical risk factors among adults diagnosed with MPNs.