Pharmacokinetics of Single-Dose Oral Stavudine in Subjects with Renal Impairment and in Subjects Requiring Hemodialysis

Two open-label studies assessed the pharmacokinetics of single orally administered doses of 40 mg of stavudine in subjects with renal impairment. In one study (study I), 15 subjects with selected degrees of renal impairment, but not requiring hemodialysis, were stratified into three groups of five subjects each according to creatinine clearance (CL CR ) normalized by body surface area (ml/min/1.73 m 2 ): mild (CL CR , 60 to 80), moderate (30 to 50), and severe (≤20) renal impairment. Five healthy subjects (CL CR ≥ 90) were also enrolled. The stavudine area under the curve from 0 h to infinity (AUC 0–∞ ) increased nonlinearly with declining renal function: 1,864, 2,215, 3,609, and 5,928 ng · h/ml for normal renal function and for mild, moderate, and severe renal impairment, respectively ( P = 0.0001 between renal impairment groups). The following stavudine dosage recommendations for renal impairment were proposed for subjects weighing ≥60 kg: CL CR of >50 ml/min/1.73 m 2 , 40 mg every 12 h; CL CR of 21 to 50 ml/min/1.73 m 2 , 20 mg every 12 h; and CL CR of 10 to 20 ml/min/1.73 m 2 , 20 mg every 24 h. For subjects weighing 0–∞ , AUC 2–6 , time to maximum concentration of drug in serum, half-life, or apparent oral clearance when the two treatment dosage regimens were compared. As a result of study II, the recommended dosing rate for subjects requiring hemodialysis was the same as that proposed for those with severe renal impairment not requiring hemodialysis; however, dosing was recommended to follow hemodialysis and to occur at the same time each day.