Novartis Institutes for BioMedical Research, Cambridge, USA.
Novartis Pharma AG, Basel, Switzerland.
Pulm Pharmacol Ther. 2020 Oct;64:101964. doi: 10.1016/j.pupt.2020.101964. Epub 2020 Oct 6.
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.
茚达特罗(IND)与格隆溴铵(GLY)和糠酸莫米松(MF)联合制成每日一次(o.d.)吸入固定剂量复方制剂(IND/GLY/MF),通过 Breezhaler®装置给药,用于哮喘的维持治疗。我们评估了吸入 IND/GLY/MF 或单药治疗后 IND、GLY 和 MF 的稳态血浆药代动力学(PK)。这是一项随机、开放标签、四交叉研究。受试者每天通过 Breezhaler®装置接受 IND/GLY/MF 150/50/160μg(高剂量)、IND 150μg、GLY 50μg 或 MF 190μg(体外细颗粒质量与 IND/GLY/MF 中的 160μg MF 相当),每个时期持续 14 天,洗脱期至少 7 天。在第 14 天进行 PK 特征分析,直至给药后 24 小时。共有 36 名健康受试者被随机分组。对于 IND,AUC0-24h,ss 和 Cmax,ss 的几何均数比值(90%CI)分别为 0.922(0.878,0.969)和 1.02(0.967,1.08),IND/GLY/MF 与 IND 单药治疗比较。对于 GLY,AUC0-24h,ss 和 Cmax,ss 的几何均数比值(90%CI)分别为 0.986(0.944,1.03)和 1.21(1.09,1.34),IND/GLY/MF 与 GLY 比较。对于 MF,AUC0-24h,ss 和 Cmax,ss 的几何均数比值(90%CI)分别为 1.16(1.09,1.24)和 1.17(1.09,1.25),IND/GLY/MF 与 MF 比较。对于所有三种单一组分,IND/GLY/MF 与单药治疗相比,均观察到相似的全身暴露,表明不存在 PK 相互作用。单独或联合使用 IND、GLY 和 MF 时,多次吸入剂量是安全且耐受良好的。当作为 IND/GLY/MF 给药时,IND、GLY 和 MF 之间不存在临床相关的药代动力学相互作用。