BENITIONSClinical Trial Intelligence

TRIple in Asthma hiGh strenGth vErsus Ics/Laba hs and tiotRopium (TRIGGER)

3期 已完成 NCT02676089

适应症Asthma
分期3期
申办方Chiesi Farmaceutici S.p.A.
状态已完成
受试者人数1,437 人
干预(药物)CHF 5993 200/6/12.5 µg, CHF 1535 200/6 µg, CHF 1535 200/6 µg + Tiotropium Respimat 2.5 µg
开始日期2016年4月6日
完成日期2018年5月28日
结果公布日2026年5月29日

摘要

Evaluate the superiority of CHF 5993 200/6/12.5 µg pressurised metered dose inhaler (pMDI) (fixed combination of extrafine beclometasone dipropionate plus formoterol fumarate plus glycopyrronium bromide) versus CHF 1535 200/6 µg pMDI (fixed combination of extrafine beclometasone dipropionate plus formoterol fumarate) in patients with uncontrolled asthma under medium doses of inhaled corticosteroid/long-acting β2-adrenergic receptor agonists (ICS/LABA), in patients with uncontrolled asthma who received medium doses of ICS/LABA. The treatments tested the improvement of the forced expiratory volume in the 1st second (FEV1) and the reduction of moderate and severe asthma exacerbations rate.

1_Change From Baseline in Pre-Dose Forced Expiratory Volume in the First Second (FEV1) at Week 26

Week 0 (pre-treatment, baseline) to Week 26. · Liter

CHF 5993 200/6/12.5 µg0.229 Liter
CHF 1535 200/6 µg0.157 Liter
CHF 1535 200/6 µg + Tiotropium (Tio) 2.5 µg0.274 Liter
p-value0.003
Least square mean difference0.073 (95% CI 0.026–0.120)

2_Moderate and Severe Asthma Exacerbation Rate Over the 52-Week Treatment Period

Week 0 (pre-treatment, baseline) to Week 52. · events/year

CHF 5993 200/6/12.5 µg1.726 events/year
CHF 1535 200/6 µg1.963 events/year
CHF 1535 200/6 µg + Tiotropium Respimat 2.5 µg1.613 events/year
p-value0.110
Adjusted rate ratio0.880 (95% CI 0.751–1.030)

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。