The Effect of Telithromycin in Acute Exacerbations of Asthma
Sebastian L. Johnston, M.D., Ph.D., Francesco Blasi, M.D., Peter N. Black, M.B., Ch.B., Richard J. Martin, M.D., David J. Farrell, Ph.D., Richard B. Nieman, M.D., for the TELICAST Investigators
Background We conducted a double-blind, randomized, placebo-controlledstudy to evaluate the efficacy of telithromycin in patientswith acute exacerbations of asthma.
Methods A total of 278 adults with diagnosed asthma were enrolledwithin 24 hours after an acute exacerbation of asthma requiringshort-term medical care. The patients were randomly assignedto receive 10 days of oral treatment with telithromycin (ata dose of 800 mg daily) or placebo in addition to usual care.Primary efficacy end points were a change from baseline overthe treatment period in symptoms (as recorded by patients ina diary card) and in the peak expiratory flow in the morningat home. The presence of Chlamydophila pneumoniae or Mycoplasmapneumoniae was ascertained by serologic analysis, polymerasechain reaction, and culture.
Results Of the two prespecified primary outcomes, only asthmasymptoms showed a significantly greater reduction among patientsreceiving telithromycin than among those receiving placebo.Mean (±SD) scores on a test of asthma symptoms (on a7-point scale, with 0 denoting no symptoms and 6 denoting severesymptoms) were 3.0±1.4 at baseline and 1.7±1.1at the end of treatment for the telithromycin group and 2.8±1.3at baseline and 2.0±1.0 at the end of treatment for theplacebo group. The mean decrease in symptom scores during thetreatment period was 1.3 for telithromycin and 1.0 for placebo(mean difference, 0.3; 95 percent confidence interval,0.5 to 0.1; P=0.004). There was no significanttreatment effect on the other primary outcome measure, a changein morning peak expiratory flow. Nausea was more common amongpatients in the telithromycin group than in the placebo group(P=0.01). Although 61 percent of patients had evidence of infectionwith C. pneumoniae, M. pneumoniae, or both, there was no relationshipbetween bacteriologic status and the response to asthma treatment.
Conclusions This study provides evidence of the benefit of telithromycinin patients with acute exacerbations of asthma; the mechanismsof benefit remain unclear. (ClinicalTrials.gov number, NCT00273520
[ClinicalTrials.gov]
.)
Source Information
From the National Heart and Lung Institute, Imperial College London (S.L.J.); and G.R. Micro (D.J.F.) both in London; the University of Milan, Istituto di Ricovero e cura a Carattere Scientifico Policlinico, Milan (F.B.); the University of Auckland, Auckland, New Zealand (P.N.B.); the National Jewish Medical and Research Center, Denver (R.J.M.); and Sanofi-Aventis, Bridgewater, N.J. (R.B.N.).
Address reprint requests to Dr. Johnston at the Department of Respiratory Medicine, National Heart and Lung Institute and Wright Fleming Institute of Infection and Immunity, Imperial College London, Norfolk Pl., London W2 1PG, United Kingdom, or at s.johnston{at}imperial.ac.uk.
Telithromycin in Acute Exacerbations of Asthma
Caramori G., Papi A., Mutgi A., Hammersley J., Kuramochi Y., Morita T., Osawa R., Andraws R., Johnston S. L., Nieman R. B., the Telithromycin, Chlamydophila, and Asthma Trial Investigators
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N Engl J Med 2006;
355:96-98, Jul 6, 2006.
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