Efficacy and safety of rasagiline as an adjunct to levodopa treatment in Chinese patients with Parkinson's disease: A randomized, double-blind, parallel-controlled, multi-centre trial

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Abstract

Rasagiline mesylate is a highly potent, selective and irreversible monoamine oxidase type B (MAOB) inhibitor and is effective as monotherapy or adjunct to levodopa for patients with Parkinson's disease (PD). However, few studies have evaluated the efficacy and safety of rasagiline in the Chinese population. This study was designed to investigate the safety and efficacy of rasagiline as adjunctive therapy to levodopa treatment in Chinese PD patients. This was a randomized, double-blind, placebo-controlled, parallel-group, multi-centre trial conducted over a 12-wk period that enrolled 244 PD patients with motor fluctuations. Participants were randomly assigned to oral rasagiline mesylate (1 mg) or placebo, once daily. Altogether, 219 patients completed the trial. Rasagiline showed significantly greater efficacy compared with placebo. During the treatment period, the primary efficacy variable - mean adjusted total daily off time - decreased from baseline by 1.7 h in patients treated with 1.0 mg/d rasagiline compared to placebo (pÂ

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Zhang, L., Zhang, Z., Chen, Y., Qin, X., Zhou, H., Zhang, C., … Li, J. (2013). Efficacy and safety of rasagiline as an adjunct to levodopa treatment in Chinese patients with Parkinson’s disease: A randomized, double-blind, parallel-controlled, multi-centre trial. International Journal of Neuropsychopharmacology, 16(7), 1529–1537. https://doi.org/10.1017/S1461145713000175

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