Bioequivalence Study of Tebipenem Pivoxil in Healthy Chinese Adults

Autor: Rui Hao, Yiming Shao, Sisi Lin, Yi Wu, Li Bian, Yiwen Zhang
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Drugs in R&D, Vol 24, Iss 1, Pp 89-96 (2024)
Druh dokumentu: article
ISSN: 1174-5886
1179-6901
DOI: 10.1007/s40268-024-00454-w
Popis: Abstract Background and Objective Tebipenem pivoxil (TP) is a carbapenem and is applied against pneumonia, otitis media, and sinusitis. This study compared the pharmacokinetics (PK) and safety of a test (T) preparation and reference (R) preparation of TP in healthy Chinese adults. Methods This study was a single-center, randomized, open, single-dose (fasting/postprandial) oral administration, two-agent, two-sequence, two-cycle, crossover bioequivalence trial. A total of 60 participants were enrolled (24 fasting and 36 postprandial). All participants were randomly assigned to the TR sequence and RT sequence. Subsequently, they switched T sequences or R sequences 7 days later. PK blood samples were collected according to the protocol, plasma TP concentration was determined by liquid chromatography-mass spectrometry, main PK parameters were calculated based on a non-compartment model, and adverse events were recorded during the test. Results In the feeding arm, the geometric mean ratio of maximum concentration (C max) was 89.84% (90% confidence interval 84.33–95.70), the geometric mean ratio of area under the plasma concentration–time curve from time 0 to last time of quantifiable concentration (AUC0–t ) was 86.80% (83.62–90.10), and the geometric mean ratio of area under the plasma concentration–time curve from time 0 to infinity time of quantifiable concentration (AUC0–∞) was 86.90% (83.73–90.20), which were within the acceptable range of bioequivalence (80–125%). In the fasting arm, the geometric mean ratio of C max was 96.07% (89.62–102.99), the geometric mean ratio of AUC0–t was 93.09% (90.47–95.78), and the geometric mean ratio of AUC0–∞ was 93.09% (90.48–95.77), which was within the acceptable range of bioequivalence (80–125%). Hence, the T preparation and R preparation of TP had bioequivalence in the fasting arm and feeding arm of the clinical trial. In addition, all adverse events were mild, and no severe adverse events were noted. Conclusion Preparations T and R of TP were bioequivalent in the fasting and postprandial groups in clinical trials, and TP was safe.
Databáze: Directory of Open Access Journals
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