Department of Clinical Pharmacology, University of Toulouse, Faculty of Medicine, 37 Allées Jules Guesde, 31000 Toulouse, France.
Expert Opin Pharmacother. 2010 Sep;11(13):2221-30. doi: 10.1517/14656566.2010.510515.
Immediate-release pramipexole (P-IR) is indicated three times daily for the symptomatic treatment of early and advanced Parkinson's disease (PD). An extended-release formulation of pramipexole (P-ER) has been developed to allow a once-daily formulation and to provide more stable dopaminergic stimulation.
This review summarizes clinical pharmacology and pharmacokinetics of P-ER for the treatment of early and advanced PD. The advantages and disadvantages of the strategies available at present for achieving continuous dopaminergic stimulation in the treatment of PD are discussed first. The pharmacological properties are then summarized. Finally, the clinical pharmacology and pharmacokinetics of P-ER are described.
The reader will gain knowledge of the development of P-ER, its current place in the pharmacotherapy of PD, and future directions.
P-ER has been shown to be efficacious in early and advanced PD and it has the same clinical profile when administered once daily as P-IR administered three times daily. An overnight switching of P-IR to dose-equivalent P-ER is successful in 80% of patients with early PD.
速释普拉克索(P-IR)每日三次用于早期和晚期帕金森病(PD)的症状治疗。已开发出普拉克索的缓释制剂(P-ER),以允许每日一次的制剂并提供更稳定的多巴胺能刺激。
本综述总结了 P-ER 治疗早期和晚期 PD 的临床药理学和药代动力学。首先讨论了目前用于实现 PD 治疗中连续多巴胺能刺激的策略的优缺点。然后总结了药理学特性。最后描述了 P-ER 的临床药理学和药代动力学。
读者将了解 P-ER 的开发、它在 PD 药物治疗中的当前地位以及未来的方向。
P-ER 已被证明在早期和晚期 PD 中有效,并且当每日一次给药时,其临床特征与每日三次给药的 P-IR 相同。80%的早期 PD 患者成功地将 P-IR 夜间转换为等效剂量的 P-ER。