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Clinical Trial
. 2001 Mar;45(3):701-5.
doi: 10.1128/AAC.45.3.701-705.2001.

Pharmacokinetics of the protease inhibitor indinavir in human immunodeficiency virus type 1-infected children

Affiliations
Clinical Trial

Pharmacokinetics of the protease inhibitor indinavir in human immunodeficiency virus type 1-infected children

D M Burger et al. Antimicrob Agents Chemother. 2001 Mar.

Abstract

The objective of this study was to evaluate the pharmacokinetics of indinavir in human immunodeficiency virus-infected children as part of a prospective, open, uncontrolled, multicenter study in The Netherlands. Human immunodeficiency virus type 1-infected children were monitored over 6 months of treatment with zidovudine (120 mg/m(2) every 8 h [q8h]), lamivudine (4 mg/kg of body weight q12h), and indinavir (33mg/kg of metabolic weight [MW] q8h). Four weeks after the start of treatment, the steady-state pharmacokinetics of indinavir were determined by high-pressure liquid chromatography. If patients had an indinavir area under the concentration-time curve (AUC) of below 10 or above 30 mg/liter. h, a dose increase or a dose reduction was made and pharmacokinetic measurements were repeated 4 weeks later. Nineteen patients started with the dose of 33 mg/kg of MW q8h. The median AUC (range) was 10.5 (2.8 to 51.0) mg/liter. h. The median AUC (range) in 17 children treated with 50 mg/kg of MW q8h was 20.6 (4.1 to 38.7) mg/liter. h. Finally, five patients had a dose increase to 67 mg/kg of MW q8h, resulting in a median AUC (range) of 36.6 (27.2 to 80.0) mg/liter. h. After 6 months of treatment, there were 11 children with an AUC of below 20 mg/liter. h, of whom 5 (45%) had a detectable viral load, while this was the case in none of the 11 children with an AUC of higher than 20 mg/liter. h. We conclude that the optimal dose of indinavir in children to obtain drug exposure similar to that observed in adult patients is 50 mg/kg of MW q8h, which approximates 600 mg/m(2) q8h. It would even be better to adjust the indinavir dose based on an AUC of greater than 20 mg/liter. h.

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Figures

FIG. 1
FIG. 1
Mean concentrations of indinavir in plasma versus time for the three dose levels and adult data for comparison.
FIG. 2
FIG. 2
Relationship between the AUC of indinavir and the virological response after 6 months of treatment. The numbers of patients in the AUC groups are as follows: five, <15 mg/liter · h; six, 15 to 20 mg/liter · h; seven, 20 to 30 mg/liter · h; four, >30 mg/liter · h. VL, viral load.

References

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    1. Burger D M, Hoetelmans R M W, Hugen P W H, Mulder J W, Meenhorst P L, Koopmans P P, Brinkman K, Keuter M, Dolmans W, Hekster Y A. Low plasma concentrations of indinavir are related to virological treatment failure in HIV-1 infected patients on indinavir-containing triple therapy. Antivir Ther. 1998;3:215–220. - PubMed
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