Single-dose pharmacokinetics of thalidomide in human immunodeficiency virus-infected patients

Antimicrob Agents Chemother. 1997 Dec;41(12):2797-9. doi: 10.1128/AAC.41.12.2797.

Abstract

The pharmacokinetics of thalidomide in nine human immunodeficiency virus-infected patients were studied. Single doses of thalidomide were well absorbed, with mean peak concentrations (+/- standard deviations) of 1.17 +/- 0.21 and 3.47 +/- 1.14 microg/ml in the 100- and 300-mg dosing groups, respectively, and the mean elimination half-life was approximately 6 h. Adverse effects were mild, with drowsiness being reported for seven of nine patients.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Female
  • HIV Infections / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Thalidomide / pharmacokinetics*

Substances

  • Thalidomide