Staab Alexander, Tillmann Christiane, Forgue S Thomas, Mackie Alison, Allerheiligen Sandra R B, Rapado Javier, Trocóniz Iñaki F
Global Pharmacokinetics/Pharmacodynamics and Trial Simulation, Lilly Research Center, Windlesham, Surrey, United Kingdom.
Pharm Res. 2004 Aug;21(8):1463-70. doi: 10.1023/b:pham.0000036922.03519.40.
To determine the population dose-response relationship for tadalafil during on-demand (as-needed) administration for treatment of erectile dysfunction (ED).
A total of 212 male patients with mild, moderate, or severe ED participated in a multicenter, randomized, double-blind, placebo-controlled, parallel-group study. Patients were randomized to receive placebo or 2, 5, 10, or 25 mg tadalafil, taken on demand over an 8-week period. Efficacy was assessed on the basis of questions 2 and 3 of the Sexual Encounter Profile (SEP) and questions 3 and 4 of the International Index of Erectile Function (IIEF) questionaires. These scores were modeled using logistic regression. A fifth patient response, the IIEF EF (erectile function) domain score, was modeled as a continuous variable.
The dose-response relationship for each efficacy variable was best described with an Emax model, in which maximum effect increased with ED severity at baseline. Response scores increased substantially between 10 and 25 mg tadalafil doses, and the dose-response parameter estimates suggested possibly higher responses at even higher doses.
Population dose-response modeling of all five oucome measures indicated that efficacy in all ED severity groups in the studied population generally increased across the 2 to 25 mg tadalafil dose range. Estimates of maximal improvement (Emax) in the IIEF EF domain score were 7.5, 11.4, and 16.3 points for patients with mild, moderate, and severe ED, respectively. Corresponding tadalafil doses to attain half-maximal improvement (ED50 estimates) were 4.7 mg, 7.1 mg, and 10.1 mg.
确定按需服用他达拉非治疗勃起功能障碍(ED)时的群体剂量反应关系。
共有212例轻度、中度或重度ED男性患者参与了一项多中心、随机、双盲、安慰剂对照、平行组研究。患者被随机分配接受安慰剂或2、5、10或25mg他达拉非,在8周内按需服用。疗效根据性活动记录简表(SEP)的问题2和问题3以及国际勃起功能指数(IIEF)问卷的问题3和问题4进行评估。这些分数采用逻辑回归建模。第五个患者反应,即IIEF勃起功能(EF)领域得分,被建模为连续变量。
每个疗效变量的剂量反应关系用Emax模型描述最佳,其中最大效应随基线时ED严重程度增加而增加。在他达拉非剂量为10至25mg之间,反应分数大幅增加,剂量反应参数估计表明,更高剂量时反应可能更高。
所有五项结果指标的群体剂量反应建模表明,在研究人群中,所有ED严重程度组在2至25mg他达拉非剂量范围内的疗效普遍增加。轻度、中度和重度ED患者在IIEF EF领域得分的最大改善估计值(Emax)分别为7.5、11.4和16.3分。达到最大改善一半(ED50估计值)的相应他达拉非剂量分别为4.7mg、7.1mg和10.1mg。