De Wit S, O'Doherty E, Edwards J, Yates R, Smith R P, Clumeck A N
C.H.U. Saint-Pierre, Brussels, Belgium.
Antimicrob Agents Chemother. 1998 Apr;42(4):903-6. doi: 10.1128/AAC.42.4.903.
D0870 is a triazole with a broad antifungal spectrum, and it has been shown to have both in vitro and in vivo activities against wild-type and fluconazole-resistant strains of Candida albicans. Twenty-two human immunodeficiency virus (HIV)-positive male subjects were enrolled in an open, nonrandomized trial investigating the pharmacokinetics of two different dosing regimens of D0870 and assessing the safety of multiple oral doses of D0870 in HIV-positive subjects and their ability to tolerate multiple oral doses. Nine subjects received an initial loading dose of 50 mg, followed by four once-daily maintenance doses of 10 mg. A further nine subjects received an initial 200-mg loading dose followed by four daily maintenance doses of 25 mg. All subjects were fasting. A single loading dose of 50 mg of D0870 resulted in a mean maximum concentration in serum (Cmax) of 107 +/- 32 ng/ml. Concentrations in plasma were maintained by the 10-mg once-daily dosing regimen as seen by the similar values of the area under the concentration-time curve from 0 to 24 h following dosing on days 1 and 5 and a mean accumulation ratio close to unity (0.90). The terminal plasma half-life of D0870 in plasma following dosing on day 5 ranged from 23 to 85 h (mean, 49 h). A single loading dose of 200 mg of D0870 resulted in a Cmax of 431 +/- 186 ng/ml. Concentrations in plasma were again maintained by the 25-mg daily dosing regimen, with the mean accumulation ratio being close to unity (1.17). The terminal half-life of D0870 in plasma following dosing on day 5 of phase II of the study ranged from 34 to 137 h (mean, 71 h). In addition, the concentrations achieved in the plasma of these HIV-positive subjects were similar to the values predicted from simulations based on data derived from normal, healthy subjects. D0870 was well tolerated. No serious adverse events were experienced during the course of the study, and all volunteers completed the trial. A total of 15 adverse events were reported, but none were considered to be related to the administration of D0870 and all had resolved by the end of the trial. No changes in the hematology, clinical chemistry, or urinalysis parameters were considered to be related to dosing with D0870. No clinically significant changes in the electrocardiogram parameters were noted during the trial. The data generated in this trial support further investigation of these regimens with HIV-positive subjects with fluconazole-susceptible or -resistant oropharyngeal candidosis.
D0870是一种具有广谱抗真菌活性的三唑类药物,已证明其在体外和体内对白色念珠菌的野生型菌株及氟康唑耐药菌株均有活性。22名人类免疫缺陷病毒(HIV)阳性男性受试者参与了一项开放、非随机试验,该试验研究了D0870两种不同给药方案的药代动力学,并评估了HIV阳性受试者多次口服D0870的安全性及其耐受多次口服剂量的能力。9名受试者接受了50mg的初始负荷剂量,随后是4次每日10mg的维持剂量。另外9名受试者接受了200mg的初始负荷剂量,随后是4次每日25mg的维持剂量。所有受试者均处于禁食状态。单次50mg负荷剂量的D0870导致血清中平均最大浓度(Cmax)为107±32ng/ml。通过每日10mg的给药方案可维持血浆浓度,在给药第1天和第5天后0至24小时浓度-时间曲线下面积值相似,且平均蓄积比接近1(0.90)可证明这一点。给药第5天后D0870在血浆中的终末血浆半衰期为23至85小时(平均49小时)。单次200mg负荷剂量的D0870导致Cmax为431±186ng/ml。血浆浓度再次通过每日25mg的给药方案得以维持,平均蓄积比接近1(1.17)。在研究的II期第5天给药后D0870在血浆中的终末半衰期为34至137小时(平均71小时)。此外,这些HIV阳性受试者血浆中达到的浓度与基于正常健康受试者数据模拟预测的值相似。D0870耐受性良好。在研究过程中未发生严重不良事件,所有志愿者均完成了试验。共报告了15起不良事件,但均被认为与D0870的给药无关,且所有不良事件在试验结束时均已缓解。未发现血液学、临床化学或尿液分析参数的变化与D0870给药有关。试验期间未观察到心电图参数有临床意义的变化。该试验产生的数据支持对这些方案在患有氟康唑敏感或耐药性口咽念珠菌病的HIV阳性受试者中进行进一步研究。