Giembycz Mark A
Department of Pharmacology and Therapeutics, Institute of Infection, Immunity and Inflammation, University of Calgary, Calgary, Alberta, Canada.
Br J Clin Pharmacol. 2006 Aug;62(2):138-52. doi: 10.1111/j.1365-2125.2006.02640.x.
Cilomilast (Ariflo, SB 207499) is an orally active, second-generation phosphodiesterase (PDE) 4 inhibitor that is being developed by GlaxoSmithkline for the treatment of chronic obstructive pulmonary disease (COPD). The results of Phase I and Phase II studies have demonstrated that cilomilast significantly improves lung function and quality of life to a clinically meaningful extent, which has led to a comprehensive Phase III programme of research evaluating efficacy, safety and mechanism of action. However, the results of those Phase III studies are unremarkable and disappointing, raising doubt over the future of cilomilast as a novel therapy for COPD. This review summarizes data obtained from the Phase III clinical development programme, highlights some of the potential concerns both specific to cilomilast and to PDE4 inhibitors in general and assesses the likelihood that cilomilast will reach the market.
西洛司特(Ariflo,SB 207499)是一种口服活性的第二代磷酸二酯酶(PDE)4抑制剂,由葛兰素史克公司研发用于治疗慢性阻塞性肺疾病(COPD)。I期和II期研究结果表明,西洛司特能在临床上显著改善肺功能和生活质量,这促使开展了一项全面的III期研究计划,以评估其疗效、安全性及作用机制。然而,那些III期研究结果并不显著且令人失望,引发了对西洛司特作为COPD新型疗法未来前景的质疑。本综述总结了从III期临床开发计划中获得的数据,突出了一些西洛司特及一般PDE4抑制剂特有的潜在问题,并评估了西洛司特上市的可能性。