A phase II study of the sterilising activities of ofloxacin, gatifloxacin and moxifloxacin in pulmonary tuberculosis
dc.contributor.author | Rustomjee R. | |
dc.contributor.author | Lienhardt C. | |
dc.contributor.author | Kanyok T. | |
dc.contributor.author | Davies G.R. | |
dc.contributor.author | Levin J. | |
dc.contributor.author | Mthiyane T. | |
dc.contributor.author | Reddy C. | |
dc.contributor.author | Sturm A.W. | |
dc.contributor.author | Sirgel F.A. | |
dc.contributor.author | Allen J. | |
dc.contributor.author | Coleman D.J. | |
dc.contributor.author | Fourie B. | |
dc.contributor.author | Mitchison D.A. | |
dc.contributor.author | Bah-Sow O.Y. | |
dc.contributor.author | Diop H. | |
dc.contributor.author | Fielding K. | |
dc.contributor.author | Gninafon M. | |
dc.contributor.author | Mitchison D. | |
dc.contributor.author | Lienhardt C. | |
dc.contributor.author | Odhiambo J. | |
dc.contributor.author | Perronne C. | |
dc.contributor.author | Portaels F. | |
dc.contributor.author | Rustomjee R. | |
dc.contributor.author | Ramjee A. | |
dc.contributor.author | Master I. | |
dc.contributor.author | Olowolagba A. | |
dc.contributor.author | Chinappa T. | |
dc.contributor.author | Osburne G. | |
dc.contributor.author | Bamber S. | |
dc.contributor.author | Pala A.S. | |
dc.contributor.author | Pillay L. | |
dc.contributor.author | Tembe C. | |
dc.contributor.author | Mpangase P. | |
dc.contributor.author | Hadebe T. | |
dc.contributor.author | Ngcobo C.P. | |
dc.contributor.author | Mkhize Z. | |
dc.contributor.author | Dlamini C.N. | |
dc.contributor.author | Gill L. | |
dc.contributor.author | Dube T. | |
dc.contributor.author | Saul M. | |
dc.contributor.author | Merle C. | |
dc.contributor.author | Suma K.F. | |
dc.date.accessioned | 2011-05-15T15:53:48Z | |
dc.date.available | 2011-05-15T15:53:48Z | |
dc.date.issued | 2008 | |
dc.description.abstract | SETTING: Current treatment for pulmonary tuberculosis (TB) might be shortened by the incorporation of fluoroquinolones (FQs). OBJECTIVES: A Phase II study aimed to assess the sterilising activities of three novel regimens containing FQs before a Phase III trial of a 4-month regimen containing gatifloxacin (GFX). DESIGN: A total of 217 newly diagnosed smear-positive patients were randomly allocated to one of four regimens: isoniazid (INH), pyrazinamide and rifampicin (RMP) with either ethambutol, GFX, moxifloxacin (MFX) or ofloxacin (OFX) for 2 months. At the end of the study, RMP and INH were given for 4 months. The rates of elimination of Mycobacterium tuberculosis were compared in the regimens using non-linear mixed effects modelling of the serial sputum colony counts (SSCC) during the first 8 weeks. RESULTS: After adjustment for covariates, MFX substitution appeared superior during the early phase of a biexponential fall in colony counts, but significant and similar acceleration of bacillary elimination during the late phase occurred with both GFX and MFX (P = 0.002). Substitution of OFX had no effect. These findings were supported by estimates of time to conversion, using Cox regression, but there were no significant differences in proportions culture-negative at 8 weeks. CONCLUSIONS: GFX and MFX improve the sterilising activity of regimens and might shorten treatment; their progression into Phase III trials therefore seems warranted. © 2008 The Union. | |
dc.description.version | Article | |
dc.identifier.citation | International Journal of Tuberculosis and Lung Disease | |
dc.identifier.citation | 12 | |
dc.identifier.citation | 2 | |
dc.identifier.issn | 10273719 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/8823 | |
dc.title | A phase II study of the sterilising activities of ofloxacin, gatifloxacin and moxifloxacin in pulmonary tuberculosis | |
dc.type | Article |