Commentary on 'Exploration of suitable pharmacodynamic parameters for acarbose bioequivalence evaluation: A series of clinical trials with branded acarbose' by Jie Huang et al.

Br J Clin Pharmacol

Division of Quantitative Methods & Modeling, Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA), Silver Spring, Maryland, USA.

Published: September 2024

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Source
http://dx.doi.org/10.1111/bcp.16148DOI Listing

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