A. Fairfax et al., A randomized, double-blind comparison of beclomethasone dipropionate extrafine aerosol and fluticasone propionate, ANN ALLER A, 86(5), 2001, pp. 575-582
Background: Inhaled corticosteroids provide first-line treatment for asthma
. An advance to improve potency was to produce new molecules with increased
glucocorticoid receptor affinity (eg, fluticasone propionate [FP]). An alt
ernative is to deliver more medication to both the large and small airway i
nflammation of asthma by using an extrafine aerosol (eg, beclomethasone dip
ropionate extrafine aerosol [BDP-extrafine]).
Objective: To demonstrate clinical equivalence of BDP-extrafine (400 mug da
ily) and FP (400 mug daily) in symptomatic asthmatic patients over the cour
se of 6 weeks.
Methods: This was a double-blind, double-dummy, parallel-group, multicenter
, 6-week study in adults with asthma taking conventional FP 1010 to 250 mug
daily or equivalent, and displaying signs/symptoms of active disease requi
ring additional therapy.
Results: Eighty-eight patients were randomized to BDP-extrafine (and FP-pla
cebo) and 84 to FP (and BDP-placebo). There were no significant differences
between treatments with respect to symptom control, as evidenced by mean c
hange from baseline in percentage days without asthma symptoms/nights witho
ut sleep disturbance observed at weeks 1 to 2, 3 to 4, or 5 to 6. Mean chan
ges from baseline in AM PEFR at weeks 5 to 6 for BDP-extrafine (19.0) and F
P (30.5) were equivalent (P = 0.022 for equivalence). There were significan
t (P < 0.001) within-treatment-group differences in mean change from baseli
ne in AM PEFR at weeks 1 to 2 for both treatments. There was no difference
in the incidence of patients reporting at least one adverse event during th
e study (BDP-extrafine 41%; FP 37%). Mean percentage change from baseline f
or AM plasma cortisol at week 6 was +17.7% for BDP-extrafine and +4.2% for
FP (P = 0.066 for difference).
Conclusions: BDP-extrafine and FP at doses of 400 <mu>g daily provided equi
valent asthma control in patients with symptomatic asthma and exhibited sim
ilar safety profiles.