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A crossover study to evaluate the pharmacokinetics and bioequivalence of hydroxychloroquine tablets in healthy Chinese subjects.

Authors :
Feng J
Kuang SY
Wan JH
Li R
Zhu YJ
Cai BL
Guan L
Zhang Z
Source :
International journal of clinical pharmacology and therapeutics [Int J Clin Pharmacol Ther] 2024 Jun; Vol. 62 (6), pp. 284-292.
Publication Year :
2024

Abstract

Aims: Hydroxychloroquine (HCQ) has a high variability and a long half-life in the human body. The purpose of this study was to evaluate the bioequivalence of a generic HCQ tablet (test preparation) versus a brand HCQ tablet (reference preparation) under fasting and fed conditions in a crossover design.<br />Materials and Methods: This was an open-label, two-period randomized, single-dose, crossover study in 47 healthy Chinese subjects who were sequentially and randomly allocated either to the fed group (high-fat meal; n = 23) or the fasting group (n = 24). Participants in each group were randomized to the two arms to receive either a single 200-mg dose of the test preparation or a 200-mg dose of the reference preparation. The application of the two preparations in each patient was separated by a 28-day washout period, regarded as sufficiently long to avoid significant interference from residual drug in the body. Whole blood samples were collected over 72 hours after drug administration.<br />Results: A total of 23 subjects completed both the fed and the fasting parts of the trial. There were no significant differences in C <subscript>max</subscript> , AUC <subscript>0-72h</subscript> , and T <subscript>1/2</subscript> between the test and reference preparation (p < 0.05). Food had no significant effect on C <subscript>max</subscript> and T <subscript>1/2</subscript> (p < 0.05), but AUC <subscript>0-72h</subscript> values were significantly reduced under fed condition compared to fasting condition (p < 0.05). The 90% confidence intervals (CIs) for the geometric mean ratios (GMRs) of C <subscript>max</subscript> and AUC <subscript>0-72h</subscript> were 0.84 - 1.05 and 0.89 - 0.98 in the fed study, and 0.97 - 1.07 and 0.97 - 1.05 in the fasting study, respectively. The carryover effect due to non-zero blood concentrations resulted in higher AUC <subscript>0-72h</subscript> values in the second period for both test and reference formulations and had no effect on the statistical results. No serious adverse events were reported.<br />Conclusion: The investigation demonstrated that the test and reference preparations are bioequivalent and well tolerated under both fasting and fed conditions in healthy Chinese subjects.

Details

Language :
English
ISSN :
0946-1965
Volume :
62
Issue :
6
Database :
MEDLINE
Journal :
International journal of clinical pharmacology and therapeutics
Publication Type :
Academic Journal
Accession number :
38577751
Full Text :
https://doi.org/10.5414/CP204406