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Pharmacokinetics of indacaterol, glycopyrronium and mometasone furoate following once-daily inhalation as a combination in healthy subjects.
Vaidya, Soniya; Jauernig, Juergen; Ethell, Brian; Abdallah, Nasri; Machineni, Surendra; Drollmann, Anton; Heudi, Olivier; Last, Stefanie; Hahn, Michael; Radhakrishnan, Rajkumar; Ignatenko, Stanislav; Tillmann, Hanns-Christian.
Afiliação
  • Vaidya S; Novartis Institutes for BioMedical Research, Cambridge, USA.
  • Jauernig J; Novartis Pharma AG, Basel, Switzerland.
  • Ethell B; Novartis Institutes for BioMedical Research, Cambridge, USA.
  • Abdallah N; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland.
  • Machineni S; Novartis Healthcare Pvt. Ltd., Hyderabad, India.
  • Drollmann A; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland.
  • Heudi O; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland.
  • Last S; Charité Research Organisation GmbH, Berlin, Germany.
  • Hahn M; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland.
  • Radhakrishnan R; Novartis Healthcare Pvt. Ltd., Hyderabad, India.
  • Ignatenko S; Charité Research Organisation GmbH, Berlin, Germany.
  • Tillmann HC; Novartis Institutes for BioMedical Research, Translational Medicine, Basel, Switzerland. Electronic address: hanns-christian.tillmann@novartis.com.
Pulm Pharmacol Ther ; 64: 101964, 2020 10.
Article em En | MEDLINE | ID: mdl-33035700
ABSTRACT
Indacaterol (IND), is co-formulated with glycopyrronium (GLY), and mometasone furoate (MF) as a once-daily (o.d.) inhaled fixed-dose combination (IND/GLY/MF) delivered via the Breezhaler® device for maintenance treatment of asthma. We evaluated the steady state plasma pharmacokinetics (PK) of IND, GLY and MF following inhalation of IND/GLY/MF or as monotherapies. This was a randomized, open-label, four-way crossover study. Subjects received IND/GLY/MF 150/50/160 µg (high-dose), IND 150 µg, GLY 50 µg or MF 190 µg (in vitro fine particle mass comparable to 160 µg MF in IND/GLY/MF) via the Breezhaler® device, o.d. for 14 days in each period, with a washout of at least 7 days. PK was characterized on Day 14, up to 24 h post-dose. In total, 36 healthy subjects were randomized. For IND, the geometric mean ratios (90% CI) for AUC0-24h,ss and Cmax,ss were 0.922 (0.878, 0.969) and 1.02 (0.967, 1.08), respectively for the IND/GLY/MF versus IND monotherapy comparison. For GLY, the geometric mean ratios (90% CI) for AUC0-24h,ss and Cmax,ss were 0.986 (0.944, 1.03) and 1.21 (1.09, 1.34), respectively for the IND/GLY/MF versus GLY comparison. For MF, the geometric mean ratios (90% CI) for AUC0-24h,ss and Cmax,ss were 1.16 (1.09, 1.24) and 1.17 (1.09, 1.25), respectively for IND/GLY/MF versus MF comparison. Similar systemic exposure was noted for IND/GLY/MF versus monotherapy for all three mono-components, indicating a lack of PK interaction. Multiple inhaled doses of IND, GLY and MF were safe and well tolerated, when administered alone or in combination. There was no clinically relevant pharmacokinetic interaction between IND, GLY and MF when administered as IND/GLY/MF.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicopirrolato Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicopirrolato Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article