4.7 Article

Bioequivalence and Pharmacokinetic Profiles of Generic and Branded Obeticholic Acid in Healthy Chinese Subjects Under Fasting and Fed Conditions

期刊

DRUG DESIGN DEVELOPMENT AND THERAPY
卷 15, 期 -, 页码 185-193

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/DDDT.S289016

关键词

obeticholic acid; bioequivalence; pharmacokinetics; food effect

资金

  1. Nanjing Zhengda Tianqing Pharmaceutical Co., Ltd.
  2. National Natural Science Foundation of China [81673519, 81803639]
  3. National major new drug creation project of China [2020ZX09201010]

向作者/读者索取更多资源

The study demonstrated the bioequivalence of a generic form of obeticholic acid and the reference drug in healthy Chinese subjects under both fasting and fed conditions, with no significant adverse events reported. Food intake may impact the main pharmacokinetic parameters of the two preparations.
Objectives: This study was conducted to evaluate the bioequivalence (BE) of a generic form of obeticholic acid (OCA) and Ocaliva (TM) under fasting and fed conditions and to determine the effects of food on the pharmacokinetic (PK) profiles of OCA in healthy Chinese subjects. Methods: A randomized, single-dose, three-sequence, three-period, partial replicated crossover study was conducted with a 21-day washout interval between periods under fasting (n=48) and fed (n=48) conditions. Blood samples for OCA and its metabolites Glyco-OCA and Tauro-OCA were collected up to 168 hours after administration in each period. PK parameters were calculated using the non-compartmental method. Geometric mean ratios for PK parameters of the test to reference drug under fasting and fed conditions and their 90% confidence intervals were estimated. Safety evaluations were carried out all through the study. Results: A total of 91 subjects completed the study with 45 in a fasted state and 46 receiving a high-fat diet. There were no serious or unexpected drug-related adverse events occurring during the study. There was no significant difference in the main PK parameters of the two preparations, irrespective of the fasting or fed conditions. Under fasting and fed conditions, the S-WR of lnC(max), lnAUC(0-t) and lnAUC(0-infinity), were 0.445, 0.370, 0.448, 0.340, 0.168, and 0.180, respectively. Thus, the average BE or the reference-scaled average BE was used to verify that the two preparations were bioequivalent under fasting and fed conditions. Compared with the fasting state, the AUC(0-t) of the test drug, the AUC(0-t), and lnAUC(0-infinity) of the reference drug were higher in the fed state. Conclusion: The test drug and the reference drug were BE and well tolerated in Chinese healthy subjects under both fasting and fed conditions. Food-intake may cause a significant difference in the main PK parameters of the two preparations.

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