The duration of action of formoterol inhaled as a dry powder formulati
on is compared with placebo and a reference treatment of salbutamol dr
y powder in patients with bronchial asthma. This single-centre, double
-blind, cross-over study recruited 23 outpatients with clinically stab
le asthma. These patients were treated with 12 mu g formoterol, 400 mu
g salbutamol or placebo in a randomly allocated sequence, with at lea
st 2 days between treatments. Forced expiratory volume in Is of expira
tion (FEV(1)) was measured at specified time points from 15 min to 15
hours post-treatment. Formoterol produced significantly higher values
of FEV(1) at the primary endpoint of 12 hours compared with placebo an
d salbutamol. No differences between FEV(1) values were seen for the a
ctive treatments of formoterol and salbutamol for the first 5 hours po
st-inhalation. Formoterol was significantly superior to placebo at all
time points, whereas salbutamol was significantly superior to placebo
for the first 5 hours. This study demonstrates that formoterol, when
given as a dry powder inhalation, has a significantly longer duration
of acute bronchodilator action than 400 mu g salbutamol inhaled as a d
ry powder. The duration of action of formoterol of at least 12 hours s
een in this study is at least as long as that reported following admin
istration from a metered dose inhaler (MDI) at the same dose level. Th
e study also demonstrates that 12 mu g formoterol dry powder is well t
olerated by patients.