Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10158576 | Pulmonary Pharmacology & Therapeutics | 2018 | 30 Pages |
Abstract
The addition of FF 10â¯Î¼g to GP MDI 28.8â¯Î¼g or 14.4â¯Î¼g in a fixed-dose combination did not appreciably alter the PK of GP, nor did an increase in GP dose from 14.4â¯Î¼g to 28.8â¯Î¼g in a fixed-dose combination with FF 10â¯Î¼g appreciably alter the PK of formoterol. Both formulations of GFF MDI and GP MDI were well tolerated in healthy Japanese subjects. Data from this study support further evaluation of GFF MDI in Japanese patients with COPD.
Keywords
tmaxλzMDIAUC0–tAUC0–12time to Cmaxterminal elimination rate constantFormoterol fumarate dihydratet½FDCGFFCmaxLLQapparent terminal elimination half-lifeLAMATEAElong-acting muscarinic antagonistLong-acting β2-agonistECGelectrocardiogramstandard deviationChronic obstructive pulmonary diseaseCOPDFixed-dose combinationlower limit of quantificationmaximum observed plasma concentrationMetered Dose InhalerCV%LSMLABACoefficient of Variationadverse eventtreatment-emergent adverse eventPharmacokineticspharmacokineticconfidence intervalCo-suspension delivery technologyLeast squares meanGlycopyrronium
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Authors
Colin Reisner, Joel Miller, Paolo DePetrillo, Andrea Maes, Shahid Siddiqui, Ubaldo J. Martin,