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A crossover study to evaluate the pharmacokinetics and bioequivalence of hydroxychloroquine tablets in healthy Chinese subjects.
- 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.
- Subjects :
- Humans
Male
Adult
Female
Young Adult
Healthy Volunteers
Asian People
Half-Life
Drugs, Generic pharmacokinetics
Drugs, Generic administration & dosage
Drugs, Generic adverse effects
Administration, Oral
China
East Asian People
Therapeutic Equivalency
Cross-Over Studies
Hydroxychloroquine pharmacokinetics
Hydroxychloroquine administration & dosage
Hydroxychloroquine adverse effects
Hydroxychloroquine blood
Tablets
Fasting
Food-Drug Interactions
Area Under Curve
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