Pharmacokinetics and safety of the two oral cefaclor formulations in healthy chinese subjects in the fasting and postprandial states
We conducted a phase I bioequivalence trial in healthy Chinese subjects in the fasting and postprandial states. The goal of this trial was to compare the pharmacokinetics and safety of the test preparation Cefaclor granule (Disha Pharmaceutical Group Co., Ltd.) and the reference preparation Cefaclor...
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Main Authors: | , , , , , , , , , , , , , , , |
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Format: | Book |
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Frontiers Media S.A.,
2022-10-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |