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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD D45ORPHA:729PV

Polycythaemia Vera

Polycythaemia Vera is a myeloproliferative neoplasm in which the bone marrow overproduces red blood cells, causing blood thickening and increased clotting risk. It is almost universally driven by the JAK2 V617F mutation. Management includes phlebotomy, aspirin, and cytoreductive therapy with hydroxyurea or ruxolitinib. The primary risk is thrombosis and transformation to myelofibrosis.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

621
Articles
185
Trials (30 AU)
Data refreshed
19 October 2026
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Common Questions

What is Polycythaemia Vera?

Polycythaemia Vera is a myeloproliferative neoplasm in which the bone marrow overproduces red blood cells, causing blood thickening and increased clotting risk. It is almost universally driven by the JAK2 V617F mutation. Management includes phlebotomy, aspirin, and cytoreductive therapy with hydroxyurea or ruxolitinib. The primary risk is thrombosis and transformation to myelofibrosis.

How many clinical trials are available for Polycythaemia Vera?

RareWays currently indexes 185 clinical trials for Polycythaemia Vera, of which 27 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Polycythaemia Vera come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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