Abstract
In two prospective, randomized studies intravenous (IV)/oral (PO) moxifloxacin (400 mg q.i.d.) was compared to IV/PO antimicrobial comparator agents for the treatment of hospitalized patients with community-acquired pneumonia. Reported here are the pooled data for the sub-population with atypical pathogens. Of 101 intent-to-treat patients with atypical pathogens, a total of 39 moxifloxacin-treated and 47 comparator-treated subjects were microbiologically valid and included in the analysis. Clinical and bacteriological success rates were 95% for the moxifloxacin-treated and 94% for the comparator-treated subjects at the test-of-cure visit. The results indicate IV/PO moxifloxacin (400 mg q.i.d.) is an effective monotherapy for patients with CAP due to atypical pathogens.
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Acknowledgments
We wish to thank all of the dedicated investigators who participated in the multinational and the North American clinical trials. We also thank B. Shearer and T. Tartaglione for editorial contributions. All experiments were performed in compliance with the current laws of the country in which they were conducted. This work was supported by a research grant from Bayer Pharmaceuticals Corporation, West Haven, CT, USA.
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Hoeffken, G., Talan, D., Larsen, L.S. et al. Efficacy and safety of sequential moxifloxacin for treatment of community-acquired pneumonia associated with atypical pathogens. Eur J Clin Microbiol Infect Dis 23, 772–775 (2004). https://doi.org/10.1007/s10096-004-1214-5
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DOI: https://doi.org/10.1007/s10096-004-1214-5