N. Vetter et al., Efficacy and safety of once-daily and twice-daily clarithromycin formulations in the treatment of acute exacerbations of chronic bronchitis, ADV THER, 16(1), 1999, pp. 13-21
The broad-spectrum antibiotic clarithromycin has been shown to be safe and
effective in the treatment of lower respiratory tract infections, including
acute exacerbations of chronic bronchitis (AECB), when dosed at 250 or 500
mg twice daily. Because a once-daily schedule may improve compliance, a mo
dified-release formulation of clarithromycin was developed. This prospectiv
e, double-blind, parallel-group, multicenter study randomized 239 patients
to receive either clarithromycin modified-release tablets 500 mg once daily
(CL MR) or clarithromycin tablets 250 mg twice daily (CL) for 7 to 14 days
. At the end of treatment, 93% of evaluable and 91% of intent-to-treat (ITT
) patients in the once-daily group and 95% and 90% of patients, respectivel
y, in the twice-daily group achieved clinical success. At 21 days posttreat
ment, clinical success rates were 86% (evaluable) and 82% (ITT) with the on
ce-daily formulation and 91% and 83% with the twice-daily formulation, Reso
lution or improvement of all symptoms occurred in 75% to 100% of patients i
n both groups. As measured by pill count, 96% and 94% of patients in the on
ce- and twice-daily groups, respectively, were more than 90% compliant with
their prescribed regimens. The most commonly reported adverse events were
abdominal pain (9%) and diarrhea (4%) in the once-daily group and abdominal
pain and headache (4% each) in the twice-daily group. CL MR is as effectiv
e as standard 250 mg CL given twice daily in the treatment of AECB. Both fo
rmulations were safe and well tolerated, and compliance with CL MR was slig
htly higher than with CL.