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Mometasone/Indacaterol/Glycopyrronium (MF/IND/GLY) and MF/IND at Different MF Strengths versus Fluticasone Propionate/Salmeterol Xinafoate (FLU/SAL) and FLU/SAL+ Tiotropium in Patients with Asthma.
van Zyl-Smit, Richard N; Chapman, Kenneth R; Kerstjens, Huib A M; Gessner, Christian; Sagara, Hironori; Tanase, Ana-Maria; Hosoe, Motoi; Pethe, Abhijit; Lawrence, David; Tillmann, Hanns-Christian; D'Andrea, Peter.
Afiliação
  • van Zyl-Smit RN; Division of Pulmonology and UCT Lung Institute, University of Cape Town, Cape Town, South Africa.
  • Chapman KR; Division of Respiratory Medicine, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Kerstjens HAM; Department of Pulmonology, University of Groningen, University Medical Center Groningen, and Groningen Research Institute for Asthma and COPD, Groningen, the Netherlands.
  • Gessner C; Universitätsklinikum Leipzig, Germany POIS Leipzig GbR, Leipzig, Germany.
  • Sagara H; Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, Tokyo, Japan.
  • Tanase AM; Novartis Pharma AG, Basel, Switzerland.
  • Hosoe M; Novartis Pharma AG, Basel, Switzerland.
  • Pethe A; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Lawrence D; Novartis Pharma AG, Basel, Switzerland.
  • Tillmann HC; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland.
  • D'Andrea P; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
J Asthma Allergy ; 16: 123-134, 2023.
Article em En | MEDLINE | ID: mdl-36714049
ABSTRACT

Background:

Once-daily, single-inhaler mometasone furoate/indacaterol acetate/glycopyrronium bromide (MF/IND/GLY, an ICS/LABA/LAMA) and MF/IND (an ICS/LABA) via Breezhaler® have been approved for the maintenance treatment of patients with asthma inadequately controlled with medium-or high-dose ICS or medium-or high-dose ICS/LABA treatment.

Objective:

Once-daily (o.d.) formulations of MF/IND/GLY and MF/IND at different MF dose strengths have been compared with twice-daily (b.i.d.) fluticasone propionate/salmeterol xinafoate (FLU/SAL), and b.i.d. FLU/SAL+ o.d. tiotropium (TIO) in the PALLADIUM, IRIDIUM and ARGON studies.

Methods:

The similarity in study design and consistent outcomes in these studies prompted the pooling of data in this review to better characterise these novel once-daily controller formulations.

Results:

Pooled data from PALLADIUM and IRIDIUM studies showed comparable or greater efficacy with o.d. MF/IND formulations versus b.i.d. FLU/SAL. The o.d. MF/IND/GLY was superior to b.i.d. FLU/SAL in the IRIDIUM study, and similar to, if not more efficacious than b.i.d. FLU/SAL + o.d. TIO in the ARGON study.

Conclusion:

These formulations therefore provide novel once-daily treatment options for patients across asthma severity and flexibility for clinicians to step-up or step-down the treatment using the same device and formulations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Asthma Allergy Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Asthma Allergy Ano de publicação: 2023 Tipo de documento: Article