Absence of clinically relevant drug interactions following simultaneous administration of didanosine-encapsulated enteric-coated bead formulation with either itraconazole of fluconazole

被引:8
作者
Damle, B [1 ]
Hess, H [1 ]
Kaul, S [1 ]
Knupp, C [1 ]
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Clin Discovery, Princeton, NJ 08543 USA
关键词
didanosine; enteric coating; antacid interaction; itraconazole; fluconazole;
D O I
10.1002/bdd.296
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This open-label, two-way crossover study was undertaken to determine whether the enteric formulation of didanosine influences the pharmacokinetics of itraconazole or fluconazole, two agents frequently used to treat fungal infections that occur with HIV infection, and whose bioavailability may be influenced by changes in gastric pH. Healthy subjects were randomized to Treatment A (200-mg itraconazole or 200-mg fluconazole) or Treatment B (same dose of itraconazole or fluconazole with 400 mg of didanosine as an encapsulated, enteric-coated bead formulation). In the itraconazole study, a lack of interaction was concluded if the 90% confidence interval (CI) of the ratio of the geometric means of log-transformed C-max and AUC(0-T) values of itraconazole and hydroxyitraconazole, the active metabolite of itraconazole, were contained entirely between 0.75 and 1.33. In the fluconazole study, the equivalence interval for C-max and AUC(0-T) was 0.80-1.25. The data showed that for itraconazole the point estimate and 90% CI of the ratios of C-max and AUC(0-T) values were 0.98 (0.79, 1.20) and 0.88 (0.71, 1.09), respectively; for hydroxyitraconazole the respective values were 0.91 (0.76, 1.08) and 0.85 (0.68, 1.06). In the fluconazole study, the point estimate and 90% CI of the ratios of C-max and AUC(0-T) values were 0.98 (0.98, 1.03) and 1.01 (0.99, 1.03), respectively. The T-max for itraconazole, hydroxyitraconazole, and fluconazole were similar between treatments. Both studies indicated a lack of clinically significant interactions of the didanosine formulation with itraconazole or fluconazole. These results showed that the encapsulated, enteric-coated bead formulation of didanosine can be concomitantly administered with drugs, such as the azole antifungal agents, whose bioavailability may be influenced by interaction with antacids. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:59 / 66
页数:8
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