Bioequivalence Analysis of Clindamycin Hydrochloride Capsules in Healthy Chinese Subjects Under Fasted and Fed Conditions.
Autor: | Wang Z; Clinical Trial Research Organization, Nancheng Hospital (Hepatobiliary Hospital), Dongguan, China.; Clinical Research Center, KangHua Hospital, Dongguan, China., Wen H; Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China., Qian X; Clinical Trial Management & Research Center, College of Pharmacy, Jinan University, Guangzhou, China., Huang M; Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China., Cheng G; Clinical Trial Management & Research Center, College of Pharmacy, Jinan University, Guangzhou, China., Zhong G; Clinical Research Center, KangHua Hospital, Dongguan, China.; Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China. |
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Jazyk: | angličtina |
Zdroj: | Clinical pharmacology in drug development [Clin Pharmacol Drug Dev] 2024 Oct 17. Date of Electronic Publication: 2024 Oct 17. |
DOI: | 10.1002/cpdd.1480 |
Abstrakt: | Clindamycin is a lincosamide antibiotic for the treatment of staphylococcal, streptococcal, and anaerobic bacterial infections. We conducted a single-center, single-dose, 2-preparation, 2-period, 2-sequence, randomized, open-label, 2 × 2 crossover study to evaluate the pharmacokinetics (PKs) and safety of the test and reference clindamycin hydrochloride capsules in healthy Chinese subjects under both fasted and fed conditions. Forty-eight subjects were enrolled in the study totally, with 24 subjects in each group. All subjects were asked to take a test or reference preparation, under either fasted or fed condition, and their blood samples were collected and assayed by a validated high-performance liquid chromatography-tandem mass spectrometry method. PK parameters including maximum plasma concentration, area under the plasma concentration-time curve from time 0 to the last concentration, and area under the plasma concentration-time curve from time 0 to infinity were estimated with noncompartmental model and analyzed. Results showed that the PK profiles of the 2 preparations were consistent and met the bioequivalence criteria. Food was identified as a factor that had an impact on clindamycin absorption. The safety of clindamycin hydrochloride capsules was satisfactory. This study proved that the 2 clindamycin hydrochloride capsules were bioequivalent in healthy Chinese subjects under both fasted and fed conditions. (© 2024, The American College of Clinical Pharmacology.) |
Databáze: | MEDLINE |
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