Acceptability of 100-mg moxifloxacin in children with rifampicin-resistant TB in three high-burden countries

Nishi Suryavanshi, Johns Hopkins Clinical Research Site
H. R. Draper, Stellenbosch University
G. Dhumal, Johns Hopkins Clinical Research Site
S. Bagchi, Johns Hopkins Clinical Research Site
N. T. Castillo-Carandang, University of the Philippines College of Medicine
A. Marthinus, Stellenbosch University
A. M.A. Cheong, De La Salle Medical and Health Sciences Institute
A. Kinikar, Byramjee Jeejeebhoy Government Medical College
M. Paradkar, Johns Hopkins Clinical Research Site
A. Gupta, Johns Hopkins University School of Medicine
J. D.R. Ocampo, University of Wisconsin School of Medicine and Public Health
M. V.G. Frias, University of the Philippines College of Medicine
D. J.O. Casalme, University of the Philippines College of Medicine
A. Hesseling, Stellenbosch University
A. J. Garcia-Prats, Stellenbosch University
M. Palmer, Stellenbosch University
G. Hoddinott, Stellenbosch University
L. Viljoen, Stellenbosch University

Abstract

BACKGROUND: Routinely, a 400-mg tablet of moxifloxacin is used in children with rifampicin-resistant TB (RR-TB), but it has very poor acceptability. We describe the acceptability of a 100-mg dispersible moxifloxacin among children and their caregivers in South Africa, India, and the Philippines. METHODS: This study is nested in a pharmacokinetics, safety, and acceptability trial of new formulations of clofazimine and moxifloxacin in children with RR-TB. Quantitative and qualitative data were collected at four time points over 24 weeks and were analysed descriptively and thematically. FINDINGS: Median age of participants (n ¼ 36) was 4.9 years. Children and caregivers from all three countries preferred the dispersible 100-mg moxifloxacin to the routine 400-mg tablet due to the relative ease of administration. The 100-mg formulation was unpalatably bitter. Children who were able to swallow the 100-mg formulation preferred to do so. The smaller size of the 100-mg tablets enhanced their ease of preparation and acceptability, although some older participants experienced the increase in the number of tablets (compared with single 400-mg tablet) as a burden. CONCLUSION: The 100-mg moxifloxacin dispersible formulation is preferred over 400-mg. Overall, moxifloxacin palatability remains sub-optimal, and there is a need to further improve the acceptability of RR-TB treatments for children.