Loading...
To assess the efficacy and safety of nabilone, a synthetic tetrahydrocannabinol analogue, as a potential treatment for some nonmotor symptoms (NMS) occurring in Parkinson disease (PD), investigators conducted a placebo-controlled, double-blind, parallel-group, enriched-enrollment randomized trial. The 47 participants had PD with an NMS scale score of ≥4 points on the Movement Disorder Society Unified PD Rating Scale-I. The study began with open-label titration of nabilone (0.25 mg once daily to 1 mg twice daily). The responders from the titration phase were then randomized 1:1 to nabilone or placebo. The change in MDS-UPDRS-I was compared at baseline prerandomization to 1-month posttreatment. The 38 patients who proceeded to a second phase …