2021
DOI: 10.2147/dddt.s289016
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Bioequivalence and Pharmacokinetic Profiles of Generic and Branded Obeticholic Acid in Healthy Chinese Subjects Under Fasting and Fed Conditions

Abstract: 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 … Show more

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Cited by 5 publications
(4 citation statements)
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“…However, these adverse reactions can be effectively alleviated after dose control and medication regimen adjustment. Obecholic Acid is subject to enterohepatic circulation, and the pharmacokinetic parameters of the active metabolites show that food may increase its absorption ( Wang et al, 2021 ).…”
Section: Obeticholic Acid (Int-747 6-ecdca 6α-ethylchenodeoxycholic A...mentioning
confidence: 99%
“…However, these adverse reactions can be effectively alleviated after dose control and medication regimen adjustment. Obecholic Acid is subject to enterohepatic circulation, and the pharmacokinetic parameters of the active metabolites show that food may increase its absorption ( Wang et al, 2021 ).…”
Section: Obeticholic Acid (Int-747 6-ecdca 6α-ethylchenodeoxycholic A...mentioning
confidence: 99%
“…Obeticholic acid (OCA), a bile acid Farnesoid X Receptor (FXR) agonist, is approved for the treatment of Primary Biliary Cholangitis (marketed as OCALIVA) and has demonstrated significant efficacy on fibrosis (improvement >1stage) with no worsening of NASH [22]. Preliminary pharmacokinetic analysis led to the selection of 2.5 mg/kg/day as the dose to be tested in the minipig to match clinical exposure obtained at the 25mg dose [23], a dose resulting in J o u r n a l P r e -p r o o f significant improvement of fibrosis in patients with NASH (See supplementary table 2). In this intervention study, minipigs were either fed CDAHFD (n=18) or chow (n=9) for 4 weeks to initiate NASH development.…”
Section: Resultsmentioning
confidence: 99%
“…BE was established by the ABE method when the 90%CIs of the GMR (test/reference) of C max , AUC 0‐t , and AUC 0‐∞ of M3 were within 80.0%–125.0%. BE was demonstrated by the RSABE method when the GMRs (test/reference) of C max , AUC 0‐t , and AUC 0‐∞ of M3 were within 80.0%–125.0%, and the upper bound of 95% CI for (Ȳ T − Ȳ R ) 2 − θS 2 WR was ≤0 10 …”
Section: Methodsmentioning
confidence: 99%