Cited by 22Statistical Methods in Clinical TrialsPharmaceutical studies and practicesDrug Solubulity and Delivery Systems

Tmax: An Unconfounded Metric for Rate of Absorption in Single Dose Bioequivalence Studies

Basson, Rodney P., Cerimele, Benito J., DeSante, Karl A., Howey, Daniel C.·1996·Pharmaceutical Research

Abstract

Purpose While peak drug concentration (Cmax) is recognized to be contaminated by the extent of absorption, it has long served as the indicator of change in absorption rate in bioequivalence studies. This concentration measure per se is a measure of extreme drug exposure, not absorption rate. This paper redirects attention to Tmax as the absorption rate variable.Methods We show that the time to peak measure (Tmax), if obtained from equally spaced sampling times during the suspected absorption phase, defines a count process which encapsulates the rate of absorption. Furthermore such count data appear to follow the single parameter Poisson distribution which characterizes the rate of many a discrete process, and which therefore supplies the proper theoretical basis to compare two or more formulations for differences in the rate of absorption. This paper urges limiting the use of peak height measures based on Cmax to evaluate only for dose-dumping, a legitimate safety concern with any formulation. These principles and techniques are illustrated by a bioequivalence study in which two test suspensions are compared to a reference formulation.Results Appropriate statistical evaluation of absorption rate via Tmax supports bioequivalence, whereas the customary analysis with Cmax leads to rejection of bioequivalence. This suggests that the inappropriate use of Cmax as a surrogate metric for absorption rate contributes to the unpredictable and uncertain outcome in bioequivalence evaluation today.

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Crossref · 10.1023/a:1016019904520

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Authors
Basson, R. P., Cerimele, B. J., DeSante, K. A., & Howey, D. C.
Affiliations
Eli Lilly (United States) (US)
Venue
Pharmaceutical Research
Published
1996-02
Volume
13
Issue
2
Pages
324-328
ISSN
  • 0724-8741 (ISSN-L)
  • 1573-904X
OpenAlex
W1563687119
Cited by
22
References
13
Citations by year
2024: 2 · 2023: 2 · 2022: 1 · 2021: 1 · 2018: 1 · 2016: 2 · 2013: 1 · 2012: 3
FWCI
0.81
Type
journal article
Language
en
Open access
closed
Locations
  • Pharmaceutical Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmaceutical studies and practices
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Drug Solubulity and Delivery Systems
Keywords
Tmax, time to peak concentration, bioequivalence, Cmax, counting processes, Poisson distribution, dose dumping, pharmacokinetics
MeSH terms
Absorption, Adult, Anti-Bacterial Agents, Chemistry, Pharmaceutical, Drug Administration Schedule, Humans, Male, Pharmacokinetics, Therapeutic Equivalency, Cross-Over Studies

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