Pharmacokinetics of nelfinavir in human immunodeficiency virus-infected infants

Academic Article

Abstract

  • Background. Nelfinavir dosed at ∼20 to 30 mg/kg three times a day (TID) in older children provides exposure similar to 750 mg TID in adults. However, the pharmacokinetics (PK) of nelfinavir in infants who are <2 years of age is not well-described. The objective of this study was to determine the pharmacokinetics of nelfinavir in infants <2 years of age. Methods. Nelfinavir concentrations were evaluated in 22 HIV-infected infants between 15 days and 2 years of age receiving nelfinavir as part of Pediatric ACTG Study 356. Nelfinavir therapy was initiated at ∼25 mg/kg TID (n = 18) or ∼55 mg/kg twice a day (n = 4) and given in combination with nevirapine, stavudine and lamivudine. PK samples were obtained predose and 1.5 and 4 h postdose at ∼6-month intervals. Eight infants (all ≤3 months of age) also had intensive PK samples collected at Week 1. Results. The median apparent clearance in the infants with intensive pharmacokinetic sampling was 2.7 liters/h/kg (range, 1.8 to ≥10) and was similar between twice a day and TID dosing cohorts. Overall nelfinavir concentrations at all collection times were lower in these infants than previously reported in older pediatric patients. Conclusions. Nelfinavir concentrations in infants are highly variable and lower than those seen in adult or older pediatric populations receiving labeled dosing. Therefore it is necessary to further evaluate nelfinavir safety, effectiveness and pharmacokinetics at higher doses than used among other pediatric populations.
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Capparelli EV; Sullivan JL; Mofenson L; Smith E; Graham B; Britto P; Becker MI; Holland D; Connor JD; Luzuriaga K
  • Start Page

  • 746
  • End Page

  • 751
  • Volume

  • 20
  • Issue

  • 8