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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

and ratio of means = 3.667 / 7.333 = 0.50

Cell migration was monitored in real time using a cultured cell monitoring system (CCM-1.4XYZ/CO2, Astec Co.) and wound closure area was measured using CCM software

Not at all

These findings are part of the reason Epitalon is often discussed in longevity medicine

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