Effect of a high‐fat and high‐calorie food on the pharmacokinetics of a novel, potent GABA analog HSK16149 in healthy subjects

Author:

Wu Qingqing123ORCID,Zhu Huijuan123,Song Rong123,Zhang Mengqi123,Li Fangqiong4,Zeng Weifang4,Wang Wei123,Jia Jingying123ORCID,Yu Chen123,Liu Yanmei123

Affiliation:

1. Drug Clinical Trial Center Shanghai Xuhui Central Hospital Shanghai China

2. Shanghai Engineering Research Center of Phase I Clinical Research & Quality Consistency Evaluation for Drugs Shanghai China

3. Shanghai Institute of Clinical Mass Spectrometry Shanghai China

4. Haisco Pharmaceutical Group Co., Ltd. Chengdu China

Abstract

AbstractHSK16149 is a novel, potent gamma‐aminobutyric acid (GABA) analog for the treatment of neuropathic pain. The purpose of this study was to assess the effect of a high‐fat and high‐calorie meal on the pharmacokinetics of HSK16149 in healthy Chinese subjects. An open‐label, two‐period crossover design was applied in this study. Twenty‐six subjects were enrolled and were randomly divided into two groups: a fasted‐fed group and a fed‐fasted group, with 13 subjects in each group. Subjects took a single oral dose of 45 mg of HSK16149 under fasted or fed conditions on Day 1 and Day 4. A series of blood samples were collected for PK analysis. Safety was evaluated throughout the study by physical examinations, clinical laboratory tests, 12‐lead ECGs, vital signs, and adverse events (AEs). The parameters AUC0‐∞, AUC0‐t, and Cmax of HSK16149 were compared to assess the bioequivalence of HSK16149 under fasted and fed conditions. The geometric mean ratios (GMRs) and their 90% confidence intervals (CIs) of AUC0‐t and AUC0‐∞ under the fed condition compared with the fasted condition were 95.84% (91.94–99.90%) and 95.79% (91.89–99.84%), respectively, which were all within the bioequivalent interval (80.00–125.00%). The GMR (90% CI) of Cmax under the fed condition compared with the fasted condition was 66.04% (59.45–73.36%), which was not within the bioequivalent range (80.00–125.00%). All adverse events were transient and resolved. This study demonstrated that HSK16149 can be administered with or without food.

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,Neurology

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