A Phase II study to evaluate the safety and efficacy of prasinezumab in early Parkinson's disease (PASADENA): Results from Part 1 Week 52

PASADENA is a Phase II, multicenter, randomized, double-blind, placebo controlled study assessing the effficacy and safety of prasinezumab, a monoclonal antibody targetting aggregated α-Syn, in individuals with early Parkinson's disease. This presentation describes the results from the first 52 weeks of the study (Part 1).

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