drugset / Trial / NCT02676089

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

NCT02676089 ↗

Phase 3 Completed 1437 enrolled Chiesi Farmaceutici S.p.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2016-04-06
Primary completion
2018-05-28
Completion
2018-05-28

Outcome

Mixed primary results

registry analysis (superiority test); CHF 5993 200/6/12.5 µg vs CHF 1535 200/6 µg; p = 0.003; Least square mean difference 0.073 (95% CI 0.026 to 0.120) NCT02676089 ↗

registry analysis (superiority test); CHF 5993 200/6/12.5 µg vs CHF 1535 200/6 µg; p = 0.110; Adjusted rate ratio 0.880 (95% CI 0.751 to 1.030) NCT02676089 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrronium Unknown 12.5 ug Inhaled
Comparator Tiotropium Other / unclassified 2.5 ug Inhaled
Comparator Formoterol Other / unclassified 6 ug Inhaled
Comparator beclomethasone dipropionate Other / unclassified 200 ug Inhaled

Indications