Safety and efficacy of newly formulated selegiline orally disintegrating tablets as an adjunct to levodopa in the management of 'off' episodes in patients with Parkinson's disease

被引:29
作者
Lew, Mark F.
Pahwa, Rajesh
Leehey, Maureen
Bertoni, John
Kricorian, Greg
机构
[1] Univ So Calif, Keck Sch Med, Div Movement Disorders, Los Angeles, CA 90033 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66103 USA
[3] Univ Kansas, Med Ctr, Parkinsons Dis & Movement Disorder Ctr, Kansas City, KS 66103 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80262 USA
[5] Univ Colorado, Hlth Sci Ctr, Movement Disorders Program, Denver, CO 80262 USA
[6] Creighton Univ, Med Ctr, Dept Neurol, Omaha, NE 68178 USA
[7] Valeant Pharmaceut Int, Aliso Viejo, CA USA
关键词
clinical study; levodopa; motor fluctuations; Parkinson's disease; selegiline orally disintegrating tablet;
D O I
10.1185/030079906X167697
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Patients receiving levodopa for Parkinson's disease experience motor fluctuations and immobility ('off' episodes) between doses. This study assessed adjunctive Zelapar dagger (selegiline orally disintegrating tablet (ODT)) for managing off episodes and for long-term safety. Methods: This open-label extension evaluated long-term safety, efficacy, and tolerability of adjunctive selegiline ODT 2.5 mg in patients who completed either of two large phase 3 double-blind studies. The study was to end after 12 months but was amended to be open-ended. Investigators could increase levodopa doses and introduce controlled-release formulations of levodopa or dopamine agonists if warranted. Additionally, results of a small randomized trial of open-label selegiline ODT 1.25 mg in comparison to conventional selegiline was added only to the safety analysis. Efficacy variables included changes in daily off time and Patient's Global Impression of Improvement (PGI-I) and Clinical Global Impressions Severity of Disease (CGI-S) ratings. Safety assessments included adverse events and oropharyngeal findings. Results: This study enrolled 254 patients: 248 from the large phase 3 studies (efficacy analysis) and an additional six from the prior open-label comparison (safety analysis) in order to evaluate a larger population for safety purposes. Mean reduction from baseline in daily off time was 9.4% (1.6h) for patients previously given selegiline ODT, 6.0% (1.2 h) for those switched from placebo, and 8.1% (1.4h) overall. PGI-I and CGI-S ratings indicated little or no change from baseline. Treatment-related adverse events occurred 132 (52%) patients. No severe oral irritations were attributed to selegiline ODT or prompted discontinuation. Conclusions: Long-term selegiline ODT 2.5 mg/day was effective, safe, and well tolerated in patients with Parkinson's disease experiencing off episodes during levodopa therapy.
引用
收藏
页码:741 / 750
页数:10
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