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Superiority of fluticasone propionate/formoterol fumarate versus fluticasone propionate alone in patients with moderate-to-severe asthma: a randomised controlled trial
被引:19
|作者:
Pertseva, Tetyana
[1
]
Dissanayake, Sanjeeva
[2
]
Kaiser, Kirsten
[3
]
机构:
[1] Dnepropetrovsk State Med Acad, Dnepropetrovsk, Ukraine
[2] Mundipharma Res Ltd, Cambridge, England
[3] Skyepharma, Muttenz, Switzerland
关键词:
Asthma;
Combination therapy;
Fluticasone propionate;
flutiform;
Formoterol fumarate;
ICS/LABA;
PELARGONIUM-SIDOIDES EPS-7630;
RESPIRATORY-TRACT ILLNESS;
HERBAL DRUG PREPARATION;
ACUTE BRONCHITIS;
DOUBLE-BLIND;
EPS;
7630;
FIXED COMBINATION;
PRIMROSE ROOT;
SCORING SYSTEM;
FLUID EXTRACT;
D O I:
10.1185/03007995.2013.825592
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objective: To demonstrate the efficacy and safety of fluticasone propionate/formoterol fumarate (flutiform*) in a pressurised metered-dose inhaler (pMDI) compared to two formulations of the fluticasone propionate component (Skyepharma fluticasone [SKP FP] or Flovent dagger, GlaxoSmithKline [GSK FP]) in adults and adolescents with moderate-to-severe asthma. Methods: Patients included in the study were >= 12 years, with symptomatic asthma for >= 1 year, steroid-requiring, had a forced expiratory volume in the first second (FEV1) of 40% to 80% (inclusive) of predicted normal values, and documented reversibility within 12 months of the study. Albuterol/salbuterol was given as rescue medication. The primary efficacy endpoint was the change in FEV1 from morning pre-dose at baseline (week 0) to 2 hours post-dose at week 12 for fluticasone/formoterol compared to SKP FP and, additionally, compared to GSK FP. Results: Fluticasone/formoterol was demonstrated to be statistically significantly superior to SKP FP. The least squares (LS) mean difference in FEV1 from baseline pre-dose to 2 hours post-dose at week 12 was 0.161 L (95% CI: 0.078, 0.245, p<0.001). Fluticasone/formoterol also demonstrated superior efficacy against GSK FP (LS mean difference = 0.185 L, 95% CI: 0.102, 0.268, p<50.001). Results from multiple secondary and tertiary efficacy endpoints assessing lung function, asthma symptoms, exacerbations and rescue medication use supported a superior efficacy of the fluticasone/formoterol combination over both fluticasone formulations. Treatment-emergent adverse events were lowest in the fluticasone/formoterol group (32.9%) compared to SKP FP (39.7%) or GSK FP (40.4%). Conclusions: Results from this study demonstrate that fluticasone/formoterol 250/10 mu g b.i.d. provides superior efficacy compared to fluticasone alone for the management of moderate-to-severe asthma, with a safety profile similar to that of fluticasone monotherapy.
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页码:1357 / 1390
页数:32
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