4.7 Article

Pharmacokinetics, Safety, and Dosing of Novel Pediatric Levofloxacin Dispersible Tablets in Children with Multidrug-Resistant Tuberculosis Exposure

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01865-18

关键词

bioavailability; children; dispersible tablets; formulation; levofloxacin; multidrug-resistant tuberculosis; pharmacokinetics

资金

  1. Joint Global Health Trials Scheme of the Department for International Development, UK (DFID)
  2. Wellcome Trust
  3. Medical Research Council (MRC UK) [MR/M007340/1]
  4. South African Medical Research Council (SA MRC) Strategic Health Innovation Partnerships (SHIP) [S003805]
  5. National Research Foundation of South Africa (NRF) [109056]
  6. Swedish Foundation for International Cooperation in Research and Higher Education (STINT grant) [SA2015-6259]
  7. South African National Research Foundation (NRF) [SA2015-6259, 101575]
  8. MRC [MR/M007340/1] Funding Source: UKRI

向作者/读者索取更多资源

This study characterized the pharmacokinetics of novel 100-mg levofloxacin dispersible tablets in 24 children aged <5 years who had household multidrug-esistant tuberculosus (MDR-TB) exposure. The current data were pooled with previously published data from children (n = 109) with MDR-TB receiving adult (250-mg) levofloxacin tablets, using nonlinear mixed-effects modelling. The adult tablets had 41% lower bioavailability than the novel dispersible tablets, resulting in much higher exposures with the dispersible tablets with the same dose.

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