Patient Endpoint Preference Project (PEPP)
The Patient Endpoint Preference Project (PEPP) investigated which symptoms matter most to people with early Parkinson’s disease, and priorities for delayed progression.
Summary
The Patient Endpoint Preference Project gathered direct patient input to inform endpoints for future trials. 511 UK participants consented through uMed's AccessPD cohort. Download the case study to see how remote participation connected patient preferences with clinical and genetic data.
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