Multicentre, randomised, parallel-group study of the efficacy and tolerability of flunisolide administered once daily via AeroChamber (R) in the treatment of mild to moderate asthma

Citation
L. Bielory et al., Multicentre, randomised, parallel-group study of the efficacy and tolerability of flunisolide administered once daily via AeroChamber (R) in the treatment of mild to moderate asthma, CLIN DRUG I, 19(2), 2000, pp. 93-101
Citations number
23
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
CLINICAL DRUG INVESTIGATION
ISSN journal
11732563 → ACNP
Volume
19
Issue
2
Year of publication
2000
Pages
93 - 101
Database
ISI
SICI code
1173-2563(200002)19:2<93:MRPSOT>2.0.ZU;2-F
Abstract
Objective: To evaluate the efficacy and tolerability of flunisolide given o nce-daily in patients with persistent asthma versus other inhaled corticost eroids given in standard multidose regimens. Patients and Methods: A total of 515 patients aged 16 to 75 years with mild to moderate asthma stabilised on multidose regimens of various inhaled cor ticosteroids were enrolled in an 8-week, open-label, multicentre, randomise d, parallel-group study. Patients were randomised in a 4:1 ratio to receive either once-daily flunisolide (1000 mu g at 6pm increased if necessary up to 2000 mu g; n = 416) administered via AeroChamber(R) or their previous co rticosteroid regimens (triamcinolone, beclomethasone or fluticasone propion ate; n = 99), which were continued on a 2- to 4-times daily basis at the pr eviously established dosages. The transfer to once-daily flunisolide from t he previous regimen was made directly without a run-in period. Results: The treatment 'success rate' [percentage of patients whose forced expiratory volume in 1 second (FEV1) values at the study end-point were at least 90% of baseline values] was 85.7% in both treatment groups. Other eff icacy parameters, including percentage predicted FEV1, morning and evening peak expiratory flow rate (PEFR) values, asthma symptom scores, salbutamol (albuterol) usage, nocturnal awakenings, quality-of-life scores and global rating of change were also similar in the two groups. The incidence of drug -related adverse events such as headache, increased cough, pharyngitis, nau sea and oral candidiasis were low in both groups (less than or equal to 1.7 % with flunisolide), and there were no notable changes in vital signs or ph ysical examination variables in either group. The majority of patients expr essed a preference for the once-daily flunisolide dosage regimen. Conclusions: Once-daily flunisolide provided asthma therapy that was at lea st as effective and as well tolerated as the patients' previous inhaled cor ticosteroid medication, indicating that individuals with mild to moderate a sthma can be directly transferred to once-daily flunisolide therapy without compromising efficacy and tolerability.