A Randomized Double-Blind Placebo-Controlled Phase III Trial of Selegiline Monotherapy for Early Parkinson Disease.

Clin Neuropharmacol

*Department of Neurology, Juntendo University School of Medicine, Tokyo; †Rehabilitation Hananoie Hospital, Tochigi; ‡Department of Neurology and Clinical Pharmacology, Ehime University Graduate School of Medicine, Ehime; §Department of Biostatistics and Clinical Epidemiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama; ∥Department of Neurology, Kyoto University Graduate School of Medicine, Kyoto; ¶Takamatsu Neurology Clinic, Takamatsu; and #All Japan Labor Welfare Foundation, Tokyo, Japan.

Published: May 2018

Background: In Japan, selegiline has been approved for combination therapy with levodopa for Parkinson disease (PD). We conducted a trial of selegiline monotherapy for early PD.

Methods: In this 12-week controlled phase III trial, a total of 292 subjects were randomized to receive placebo (n = 146) (full analysis set 140) or selegiline (n = 146) (full analysis set 139). The primary outcome measure was the change in the Unified Parkinson Disease Rating Scale part I + II + III total score from baseline to the final visit. Other secondary measures and a safety profile were evaluated.

Results: Selegiline monotherapy reduced the primary outcome measure by -6.26 ± 7.86 compared with the placebo -3.14 ± 6.98 (mean ± SD, P = 0.0005 by analysis of covariance). There was no significant difference in the number of adverse events between the 2 groups (P > 0.05).

Conclusions: Selegiline monotherapy reduced the total Unified Parkinson Disease Rating Scale part I + II + III score and was well tolerated in Japanese patients with early PD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610558PMC
http://dx.doi.org/10.1097/WNF.0000000000000239DOI Listing

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