W. Storms et al., Clinical safety and tolerability of montelukast, a leukotriene receptor antagonist, in controlled clinical trials in patients aged >= 6 years, CLIN EXP AL, 31(1), 2001, pp. 77-87
Objective Montelukast is a leukotriene receptor antagonist administered ora
lly once daily for treatment of chronic asthma in adults and children. A co
mprehensive analysis of safety data from double-blind, randomized, placebo-
controlled trials with montelukast has not been previously reported.
Patients and methods A pooled analysis of safety data from 11 multicentre,
randomized, controlled montelukast Phase IIb and III trials and five long-t
erm extension studies was performed. A total of 3386 adult patients (a,oed
15-85 years) and 336 paediatric patients (aged 6-14 years) were enrolled in
the trials; 2031 adults received montelukast for up to 4.1 years, and 257
children received montelukast for up to 1.8 years. Summary statistics compa
ring incidences of adverse events among treatment groups were calculated.
Results The overall incidence of clinical and laboratory adverse events amo
ng montelukast-treated patients, both adult and paediatric, was similar to
that among patients receiving placebo. There were no clinically relevant di
fferences in individual adverse events, including infectious upper respirat
ory conditions and transaminase elevations, between montelukast and placebo
groups. Discontinuations due to adverse events occurred with similar frequ
encies during placebo, montelukast and inhaled beclomethasone therapy. No d
ose-related adverse effects of montelukast were observed in adults treated
with dosages as high as 200 mg per day (20 times the recommended dose) for
5 months. This tolerability profile montelukast observed in clinical trials
has been generally reflected in the post-marketing safety experience seen
to date.
Conclusion These data indicate a tolerability profile for montelukast simil
ar to placebo during both short-term and long-term administration, even at
doses substantially higher than the recommended clinical dose of 10 mg once
daily for adults and 5 mg once daily for children aged 6-14 years.