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Our mission is to make life easier for people with MPN. For this purpose we bring doctors and researchers together so that we are getting closer to our common goal.


Through the creation of a Swiss registry, we ensure that treatment and illness data is optimally recorded.  

We encourage clinical research into MPN as well as improving the care of all MPN patients. 

In order to facilitate global research projects, we network researchers and support the exchange of data with other international MPN registration authorities.

These include the University of Cambridge, the German Study Group for Myeloproliferative Neoplasias (GSG-MPN) and the Grupo Espanol de Enfermedades Mieloproliferativas Cronicas Filadelfia negatives (GEMFIN). 

It is also our aim to enable an MPN research grant to gain further knowledge in this area and get one step closer to curing the disease. 

Hospital Employees
Laboratory Scientist


Our Swiss registry enables the optimal  management and use of disease data. We have developed clear standards for collecting the data. 

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