FOR RESEARCHERS AND CLINICIANS
Resources for Today’s MPN Researcher and Clinician
At MPN Research Foundation, we’re different than other research funding organizations. As an organization that is founded by and funded by patients, we’re primarily influenced by the needs and concerns of MPN patients – the people who are most affected by myelofibrosis, essential thrombocythemia, and polycythemia vera.
MPN Research Foundation resources for researchers include:
- Apply for a Grant – Discover how to apply for a MPN Research Foundation grant.
- Request information kits or newsletters for your PV, ET, and MF patients
- MPN Science Report – Explore recent MPN research and science reports
- MPN Roundtable – See how we’re bridging the gap between industry and academia through the annual MPN Roundtable.
- MPN Neutrality Policy – View our statement of independence
