Pharmacokinetics of indacaterol, glycopyrronium and mometasone furoate administered as an inhaled fixed-dose combination in Japanese and Caucasian healthy subjects

被引:7
作者
Inoue, Satoru [1 ]
Vaidya, Soniya [2 ]
Tillmann, Hanns-Christian [3 ]
Sakita, Yohei [1 ]
Machineni, Surendra [4 ]
Heudi, Olivier [3 ]
Furihata, Kenichi [5 ]
机构
[1] Novartis Pharma KK, Tokyo, Japan
[2] Novartis Inst BioMed Res, Cambridge, MA USA
[3] Novartis Inst BioMed Res, Basel, Switzerland
[4] Novartis Healthcare Pvt Ltd, Hyderabad, India
[5] Keikokai Med Corp, P One Clin, Tokyo, Japan
关键词
Indacaterol; glycopyrronium; mometasone furoate; Pharmacokinetics; Japanese-Caucasian; Asthma;
D O I
10.1186/s12890-020-01382-6
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BackgroundA once-daily (o.d.) fixed-dose combination of indacaterol acetate (IND), glycopyrronium bromide (GLY), and mometasone furoate (MF) delivered via the Breezhaler((R)) device (IND/GLY/MF) is being developed for treatment of asthma. This study compared steady-state pharmacokinetics of IND, GLY and MF between Japanese and Caucasian male subjects after multiple inhalations of IND/GLY/MF o.d.MethodsThis was a single-center, open-label, 2-treatment crossover study with a 21-day washout period. Japanese and Caucasian subjects received IND/GLY/MF 150/50/80 mu g (inhaled corticosteroid [ICS] medium-dose) or 150/50/160 mu g o.d. (ICS high-dose) for 14 days in each period. Pharmacokinetics were characterized up to 24 h post-dose on Days 1 and 14.ResultsIn total, 16 Japanese (median age 31 years [range 20-40 years], mean weight 68.3 kg) and 17 Caucasian subjects (median age 27 years [range 21-43 years], mean weight 75.0 kg) were randomized. Geometric mean ratios (Japanese/Caucasian) [90% confidence interval (CI)] for C-max for IND, GLY and MF at the high ICS dose on Day 14 were 1.31 [1.13, 1.51] 1.38 [1.13, 1.69] and 1.07 [0.969, 1.18], respectively. Geometric mean ratios (Japanese/Caucasian) [90% CI] for AUC(0-24h) on Day 14 for IND, GLY and MF at the high ICS dose were 1.17 [1.01, 1.35], 1.05 [0.920, 1.20] and 1.15 [1.05, 1.27] respectively. Similar trends were noted for all components for the medium ICS dose treatment. IND/GLY/MF was safe and well tolerated; no AEs suspected to be study drug-related were observed.ConclusionPharmacokinetics of IND, GLY and MF (high and medium dose) when delivered as a fixed-dose combination were comparable between Japanese and Caucasian subjects. The IND/GLY/MF combination at the administrated doses was safe and well tolerated in both ethnic groups.Trial registrationJapan Registry of Clinical Trial: jRCT2031200227, retrospectively registered on 04, December, 2020.
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页数:12
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