Wasmuth Jan-Christian, la Porte Charles J L, Schneider Katrin, Burger David M, Rockstroh Juergen K
Department of Internal Medicine I, University of Bonn, Germany.
Antivir Ther. 2004 Apr;9(2):213-20.
To assess the pharmacokinetics and tolerability of reduced dosages of twice daily indinavir (IDV) boosted by low-dose ritonavir (RTV) in healthy volunteers.
Pharmacokinetics and tolerability of IDV/RTV twice daily (600/100 mg and 400/100 mg) were assessed in a randomized crossover design in 16 healthy volunteers. Each dosage was taken twice daily for 2 weeks before 12 h pharmacokinetics were obtained.
Sixteen subjects were included, with a mean age +/- SD of 30 +/- 4 years; seven female, nine male. Fifteen subjects completed the study. After dose reduction of IDV AUC, Cmax and Cmin decreased significantly. In the 400 mg group three out of 15 subjects had IDV levels below 0.10 mg/l vs none in the 600 mg group. All subjects reported mild to moderate side effects throughout the study period, which were more severe in the 600 mg group (mostly renal, dry skin/lips, paresthesias/oral discomfort). In the 600 mg group four subjects reported dysuria and one subject discontinued because of flank pain, whereas two subjects reported dysuria and no subject discontinued in the 400 mg group, respectively. Eight subjects developed crystalluria without a significant difference between both groups. No significant change in serum creatinine was observed.
IDV/RTV 400/100 mg twice daily resulted in significant lower IDV exposure, with three out of 15 subjects revealing Cmin values below the recommended threshold for wild-type virus of 0.10 mg/l. Tolerability, however, was lower in the 600 mg IDV group. Therapeutic drug monitoring in the individual patient appears to be necessary to guarantee appropriate drug levels and simultaneously minimize toxicity.
评估在健康志愿者中,低剂量利托那韦(RTV)增强的每日两次低剂量茚地那韦(IDV)的药代动力学和耐受性。
在16名健康志愿者中采用随机交叉设计评估每日两次IDV/RTV(600/100毫克和400/100毫克)的药代动力学和耐受性。每种剂量每日服用两次,持续2周,然后获取12小时的药代动力学数据。
纳入16名受试者,平均年龄±标准差为30±4岁;7名女性,9名男性。15名受试者完成了研究。IDV剂量降低后,AUC、Cmax和Cmin显著下降。在400毫克组中,15名受试者中有3名的IDV水平低于0.10毫克/升,而600毫克组中无人低于此水平。在整个研究期间,所有受试者均报告有轻度至中度副作用,600毫克组更为严重(主要是肾脏问题、皮肤/嘴唇干燥、感觉异常/口腔不适)。在600毫克组中,4名受试者报告排尿困难,1名受试者因胁腹痛停药,而在400毫克组中,分别有2名受试者报告排尿困难,但无人停药。8名受试者出现结晶尿,两组之间无显著差异。未观察到血清肌酐有显著变化。
每日两次服用IDV/RTV 400/100毫克导致IDV暴露显著降低,15名受试者中有3名的Cmin值低于野生型病毒推荐阈值0.10毫克/升。然而,600毫克IDV组的耐受性较低。对个体患者进行治疗药物监测似乎有必要,以确保药物水平合适并同时将毒性降至最低。