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Pharmacokinetics of Stavudine and Didanosine Coadministered with Nelfinavir in Human Immunodeficiency Virus-Exposed Neonates
Authors:Chokechai Rongkavilit   Pimolrat Thaithumyanon   Theshinee Chuenyam   Bharat D. Damle   Sompop Limpongsanurak   Chantana Boonrod   Aeumporn Srigritsanapol   Elly A. M. Hassink   Richard M. W. Hoetelmans   David A. Cooper   Joep M. A. Lange   Kiat Ruxrungtham     Praphan Phanuphak
Affiliation:HIV Netherlands-Australia-Thailand Research Collaboration, Thai Red Cross AIDS Research Centre, Bangkok, Thailand. crongkav@dmc.org
Abstract:We evaluated the pharmacokinetics of stavudine (d4T) and didanosine (ddI) in neonates. Eight neonates born to human immunodeficiency virus-infected mothers were enrolled to receive 1 mg of d4T per kg of body weight twice daily and 100 mg of ddI per m(2) once daily in combination with nelfinavir for 4 weeks after birth. Pharmacokinetic evaluations were performed at 14 and 28 days of age. For d4T, on days 14 and 28, the median areas under the concentration-time curves from 0 to 12 h (AUC(0-12)s) were 1,866 and 1,603, ng x h/ml, respectively, and the median peak concentrations (C(max)s) were 463 and 507 ng/ml, respectively. For ddI, on days 14 and 28, the median AUC(0-10)s were 1,573 and 1,562 h x ng/ml, respectively, and the median C(max)s were 627 and 687 ng/ml, respectively. Systemic levels of exposure to d4T were comparable to those seen in children, suggesting that the pediatric dose of 1 mg/kg twice daily is appropriate for neonates at 2 to 4 weeks of age. Levels of exposure to ddI were modestly higher than those seen in children. Whether this observation warrants a reduction of the ddI dose in neonates is unclear.
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