Posted in partnership: Would you like to take part in a virtual focus group with people affected by plantar fibromatosis in the United States? ICON plc and Endo Pharmaceuticals Inc. which is conducting research on an investigational treatment for plantar fibromatosis, are hosting focus groups to better understand the experiences of people affected by plantar fibromatosis in the USA and how it impacts their lives. They are looking for 16 people who are living with plantar fibromatosis. Participants will be offered $200 as compensation. Focus groups will take place in May/June 2022. Please contact Ms. Laura Iliescu, Director of Patient Advocacy, ICON plc at iliesculaura@prahs.com for more information if you would like to take part.
My experience with Ledderhose disease aka plantar fibromatosis. This information is not intended to replace your doctor. Information on this blog is provided for informational purposes only. You should not use the information on this web site for diagnosing or treating.
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