Bioequivalence study of fluticasone propionate nebuliser suspensions in healthy Chinese subjects

• Published in: Frontiers in pharmacology 2025-01, Vol.15, p.1452596
• Main Authors: Cheng, Feng, Shen, Tao, Zhang, Fucheng, Lei, Chenghao, Zhu, Ye, Luo, GuoJun, Xiao, Dawei
• Format: Article
• Language: English
• Subjects: asthma; bioequivalence; fluticasone propionate; healthy Chinese subjects; safety
• ISSN: 1663-9812; 1663-9812
• DOI: 10.3389/fphar.2024.1452596

Fluticasone propionate is a synthetic trifluoro-substituted glucocorticoid, a highly selective glucocorticoid receptor agonist. Fluticasone propionate nebuliser suspensions is an inhaled corticosteroid with the low systemic bioavailability which provides a low risk (benefit outcome without the adverse effects that accompany systemically administered corticosteroids), referred as a first-line preventive agent for patients with persistent asthma. China has become one of the countries with the highest asthma mortality rate in the world in the past years. It urgently needs good generic drugs to help ease patients' burden and improve their quality of life. The primary objective of this study was to evaluate the bioequivalence of fluticasone propionate nebuliser suspensions between test formulation (generic product) and reference formulation (original product, Flixotide Nebules ) with the pharmacokinetic parameters as the endpoint indicators and the secondary objective was to evaluate the safety of two inhalated fluticasone propionate nebuliser suspensions under the condition of fasting in healthy Chinese subjects. The bioequivalence study was conducted with a single-center, randomized, open-label, single-dose, two sequences, two-period crossover design. 24 healthy subjects were randomly assigned into T-R and R-T sequence groups with 12 patients in each group. The subjects were administered 1 mg (2 mL:0.5 mg,plastic ampoules) of generic fluticasone propionate nebuliser suspension as a test formulation or Flixotide Nebules as reference formulation and cross administration after sufficient washout period (5 days) for the second period study. The blood sample was collected at predetermined time points up to 48 h and the plasma concentration of fluticasone propionate was determined by HPLC-MS/MS in healthy subjects after inhalation of test or reference formulation. The non-compartment model method (NCA module) of the WinNonlin software (version 8.3) was used to calculate the pharmacokinetic parameters (C , AUC AUC ) between the test formulation and the reference formulation were within the predefined range of 80.00% and 125.00%, bioequivalence of both formulations was demonstrated. The 90% confidence intervals of the T/R ratio of the geometric mean of C , AUC , and AUC for both formulations were 90.24%-112.68%, 96.99%-112.27% and 96.41%-111.59% respectively, which were all within the bioequivalent range of 80%-125%. No severe, suspicious or unexpected serious advers