Journal article
Clarithromycin therapy for patients with Cystic Fibrosis: A randomized controlled trial
P Robinson, MS Schechter, PD Sly, K Winfield, J Smith, S Brennan, M Shinkai, MO Henke, BK Rubin
Pediatric Pulmonology | Published : 2012
DOI: 10.1002/ppul.21613
Abstract
The clinically significant actions of oral azithromycin in modifying progressive cystic fibrosis (CF) lung disease have been well documented. In vitro and clinical data suggests that clarithromycin has immunomodulatory properties similar to other 14-member macrolides, however two previously reported short term, open label trials of clairthromycin in small numbers of patients with CF failed to show significant benefits in modifying lung function or inflammation. We performed an international double blind, cross-over trial in which 63 subjects with CF were studied while receiving either placeo or 500mg oral clarithromycin twice daily for 5 months, with a 1-month wash-out. The primary efficacy ..
View full abstractGrants
Funding Acknowledgements
This study was funded by research grants to BKR from the United States Cystic Fibrosis Foundation, Abbott Laboratories, and the NIH (GCRC Grant to Wake Forest University). We appreciate the assistance of Kay Ashburn RN and Walter Ambrosius, PhD in conducting this study.Funding source: Cystic Fibrosis Foundation, Abbott Laboratories, NIH, GCRC Grant.