The aim of the clinical study reported here was to investigate the eff
icacy of salmeterol, a new long-acting selective beta(2)-agonist, in p
atients with bronchial asthma. Twenty-four children with moderate asth
ma were enrolled in the longitudinal study, consisting of a run-in per
iod of 2 weeks followed by a treatment period of 4 weeks. Maintenance
treatment consisted of inhaled corticosteroid and disodium cromoglycat
e, or both, at the same daily dose throughout the study. During the ru
n-in period, the patients continued to inhale salbutamol when needed a
nd some of them (37%) also received theophylline. They were subsequent
ly treated with salmeterol 50 mu g twice daily and pm salbutamol for 4
weeks. Efficacy was evaluated using symptom scores and pulmonary func
tion tests including forced vital capacity parameters, pulmonary volum
es, airway resistance and specific airway conductance that were measur
ed sensitively by a whole body plethysmograph. As a result, salmeterol
produced significant improvement in morning and evening peak expirato
ry flow rates, vital capacity, airway resistance, conductance and asth
ma symptoms versus salbutamol and theophylline. Adverse reactions were
judged to be mild and few.