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KMID : 0363620100310030001
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Journal of Korean Oriental Medicine
2010 Volume.31 No. 3 p.1 ~ p.7
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Interpretation of Animal Dose and Human Equivalent Dose for Drug Development
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Shin Jang-Woo
Seol In-Chan
Son Chang-Gue
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Abstract
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Objectives: To introduce to TKM scientific dose conversion methods of human to animal or animal to human for new drug investigations.
Methods: We searched guidelines of the FDA and KFDA, and compared them with references for drug-dose conversion from various databases such as PubMed and Google. Then, we analyzed the potential issues and problems related to dose conversion in safety documentation of new herbal drugs based on our experiences during Investigational New Drug (IND) applications of TKM.
Results: Dose conversion from human to animal or animal to human must be appropriately translated during new drug development. From time to time, investigators have some difficulty in determining the appropriate dose, because of misunderstandings of dose conversion, especially when they estimate starting dose in clinical or animal studies to investigate efficacy, toxicology and mechanisms. Therefore, education of appropriate dose calculation is crucial for investigators. The animal dose should not be extrapolated to humans by a simple conversion method based only on body weight, because many studies suggest the normalization method is based mainly on body surface area (BSA). In general, the body surface area seems to have good correlation among species with several parameters including oxygen utilization, caloric expenditure, basal metabolism, blood volume and circulating plasma protein. Likewise, a safety factor should be taken into consideration when deciding high dose in animal toxicology study.
Conclusion: Herein, we explain the significance of dose conversion based on body surface area and starting dose estimation for clinical trials with safety factor.
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KEYWORD
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clinical trial, dose conversion, safety factor, body surface area
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