Results of the first randomized, placebo¹-controlled long-term clinical trial show the investigational² drug safinamide may reduce dyskinesia（运动障碍） or involuntary movements（非随意运动） in mid-to-late stage Parkinson's disease. The findings will be presented as late-breaking research at the 63rd Annual Meeting of the American Academy of Neurology, April 9, 2011, in Honolulu. "Our findings over a two-year treatment period suggest that taking safinamide in addition to levodopa（左旋多巴） and other dopaminergic treatments could help patients who continue to experience tremors⁴ and involuntary movement problems," said study author Ravi Anand, MD, a consultant⁵ with Newron Pharmaceuticals⁶ in Bresso, Italy. "These results are an important step forward in understanding how safinamide impacts patients with severe Parkinson's disease. Symptoms of Parkinson`s disease, motor fluctuations⁷ and dyskinesia can greatly affect a person's daily living and quality of life."

For the two-year study, 669 patients with mid-to-late stage Parkinson's disease who were already taking levodopa and other dopaminergic treatments were given 50 or 100 milligrams of safinamide per day or a placebo pill. Scientists tested participant's movement ability using the United Parkinson's disease rating scale that measures activities such as tremor³, speech, behavior, mood and daily activities including swallowing, dressing⁸ and walking. A specific tool measuring severity of dyskinesia（运动障碍） (DRS) was used in addition as primary efficacy endpoint.

At the start of the study, patients who took the 50 milligram dose of safinamide had an average score of 3.9 compared to a score of 3.4 for those taking a placebo pill. Patients who took the 100 milligram dose had an average score of 3.7.

After two years, researchers discovered in a post-hoc analysis that safinamide at 100 milligrams a day on top of taking levodopa reduced dyskinesia, or movement problems, by 24 percent in the one-third of participants who had scored a four or higher on the dyskinesia rating scale at the beginning of the study compared to those taking a placebo. There were no significant differences for people who took the 50 milligram dose.

There were no significant differences in the primary efficacy measure (movement control, i.e., dyskinesia) scores in the overall population. Side effects were comparable among the three treatment groups.