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12-Week Study: Efficacy and Safety Overview A 12-week, Phase 3, randomized, double-blind, double-dummy study evaluated the efficacy, safety, and tolerability of continuous 24-hour subcutaneous infusion of PRODUODOPA versus oral immediate-release (IR) levodopa/carbidopa (LD/CD) in patients with advanced Parkinsons disease (PD) and severe motor fluctuations

For instance, some people report a slight headache, dizziness, or a reaction at the injection site

12 Biomechanical testing demonstrated significant improvements in the stability of the DRUJ for both groups

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