Fixed-dose combination of indacaterol/glycopyrronium/mometasone furoate once-daily versus salmeterol/fluticasone twice-daily plus tiotropium once-daily in patients with uncontrolled asthma: A randomised, Phase IIIb, non-inferiority study (ARGON)

被引:50
|
作者
Gessner, Christian [1 ]
Kornmann, Oliver [2 ]
Maspero, Jorge [3 ]
van Zyl-Smit, Richard [4 ,5 ]
Kruell, Matthias [6 ]
Salina, Anna [7 ]
Gupta, Pritam [8 ]
Bostel, Sebastien [7 ]
Fucile, Sebastian [9 ]
Conde, Lorena Garcia [7 ]
Pfister, Pascal [7 ]
机构
[1] Univ Klinikum Leipzig, Germany POIS Leipzig GbR, Leipzig, Germany
[2] IKF Pneumol Frankfurt, Clin Res Ctr Resp Dis, Frankfurt, Germany
[3] Fdn CIDEA, Allergy & Resp Res Unit, Buenos Aires, DF, Argentina
[4] Univ Cape Town, Div Pulmonol, Cape Town, South Africa
[5] Univ Cape Town, UCT Lung Inst, Cape Town, South Africa
[6] Inst Allerg & Asthmaforsch Berlin, IAAB, Berlin, Germany
[7] Novartis Pharma AG, Basel, Switzerland
[8] Novartis Healthcare Pvt Ltd, Hyderabad, India
[9] Novartis Pharmaceut, E Hanover, NJ USA
关键词
Indacaterol/glycopyrronium/mometasone; Salmeterol/fluticasone; Tiotropium; AQLQ; Non-inferiority; Lung function; DRY POWDER INHALER; FLUTICASONE PROPIONATE; MOMETASONE FUROATE; DAILY SALMETEROL; EFFICACY; SAFETY; CORTICOSTEROIDS; COPD; INDACATEROL; PERSISTENCE;
D O I
10.1016/j.rmed.2020.106021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The efficacy and safety of once-daily (o.d.) fixed-dose combination of indacaterol (IND), glycopyrronium (GLY) and mometasone furoate (MF) via Breezhaler (R) versus concurrent administration of salmeteml/fluticasone (SAL/FLU) twice-daily (b.i.d.) via Accuhaler (R)+Tiotropium (TIO) o.d. via Respimat (R) was evaluated in patients with uncontrolled asthma. Methods: Patients (aged >= 18 years), symptomatic (Asthma Control Questionnaire [ACQ]-7 >= 1.5) despite treatment with long-acting beta(2)-agonist/inhaled corticosteroid medium- or high-dose, received IND/GLY/MF high-(150/50/160 mu g) or medium-dose (150/50/80 mu g) o.d. or SAL/FLU high-dose (50/500 mu g) b.i.d.+Tio 5 mu g o.d. for 24 weeks. The primary objective was to confirm the non-inferiority of either dose of IND/GLY/MF to SAL/FLU high dose + TIO in terms of Asthma Quality of Life Questionnaire (AQLQ). Additional endpoints: ACQ-7, lung function, health status (St George's Respiratory Questionnaire [SGRQ]), exacerbations, and safety after 24 weeks. Results: IND/GLY/MF high- and medium-dose met the primary endpoint, confirming non-inferiority to SAL/FLU high dose + TIO for AQLQ (least square mean treatment difference [Delta]: 0.073 and -0.038, respectively; both p < 0.001). IND/GLY/MF high-dose improved ACQ-7 (Delta: -0.124; p = 0.004), trough FEV1 (Delta: 96 mL; p < 0.001), peak expiratory flow (morning [Delta: 9.56 L/min; p = 0.005], evening [Delta: 9.15 L/min; p = 0.006]) and SGRQ (Delta: -2.00; p = 0.04) versus SAL/FLU high dose + TIO. Improvements in these endpoints were comparable for IND/GLY/MF medium-dose and SAL/FLU high dose + TIO. Adverse events were generally comparable across treatments. Conclusions: IND/GLY/MF high- and medium-dose o.d. via a single inhaler were non-inferior to SAL/FLU high-dose b.i.d. + TIO o.d. via two inhalers for AQLQ. IND/GLY/MF high-dose o.d. improved lung function, asthma control and health status versus SAL/FLU high dose + TIO, while IND/GLY/MF medium-dose had comparable efficacy but at a corresponding lower steroid dose.
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页数:10
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