Novel direct curve comparison metrics for bioequivalence
- PMID: 11474775
- DOI: 10.1023/a:1011067908500
Novel direct curve comparison metrics for bioequivalence
Abstract
Purpose: The object of this work was to devise four new direct curve comparison (DCC) metrics and examine each metric's distribution properties and performance characteristics.
Methods: DCC metrics, Cmax, and AUCi were calculated from two bioequivalence studies of three sustained release carbamazepine formulations, where a range of profile similarity was observed. DCC metric values and their confidence intervals were compared to Cmax and AUCi.
Results: The DCC metrics rho, rhom, deltaa, and deltas, exhibited more favorable distributions than Cmax and AUCi ratios, which were frequently skewed. The DCC metrics performed differently than Cmax and AUCi ratios in profile comparisons due to the nature of the DCC metrics. Unlike Cmax and AUCi, the DCC metrics utilize all data points to directly compare entire profiles. Each DCC metric appears to measure "exposure" in a single assessment. Possible bioequivalence acceptance criteria are: p < or =1.40, rhom, < or =0.35, deltaa, < or =0.27, and deltas < or =0.102.
Conclusions: These DCC metrics, particularly rhom, are promising bioequivalence metrics for "exposure."
Comment in
-
Determination of in vivo bioequivalence.Pharm Res. 2002 Mar;19(3):227-8. doi: 10.1023/a:1014422430027. Pharm Res. 2002. PMID: 11934226
Similar articles
-
Criteria to assess in vivo performance and bioequivalence of generic controlled-release formulations of carbamazepine.Epilepsia. 1998 May;39(5):513-9. doi: 10.1111/j.1528-1157.1998.tb01414.x. Epilepsia. 1998. PMID: 9596204 Clinical Trial.
-
Generic-reference and generic-generic bioequivalence of forty-two, randomly-selected, on-market generic products of fourteen immediate-release oral drugs.BMC Pharmacol Toxicol. 2017 Dec 8;18(1):78. doi: 10.1186/s40360-017-0182-1. BMC Pharmacol Toxicol. 2017. PMID: 29216899 Free PMC article. Clinical Trial.
-
Carbamazepine: a bioequivalence study and limited sampling modeling.Int J Clin Pharmacol Ther. 2002 Sep;40(9):424-30. doi: 10.5414/cpp40424. Int J Clin Pharmacol Ther. 2002. PMID: 12358160 Clinical Trial.
-
The bioequivalence of highly variable drugs and drug products.Int J Clin Pharmacol Ther. 2005 Oct;43(10):485-98. doi: 10.5414/cpp43485. Int J Clin Pharmacol Ther. 2005. PMID: 16240706 Review.
-
Metrics for the evaluation of bioequivalence of modified-release formulations.AAPS J. 2012 Dec;14(4):813-9. doi: 10.1208/s12248-012-9396-8. Epub 2012 Aug 22. AAPS J. 2012. PMID: 22910857 Free PMC article. Review.
Cited by
-
Trapezoid bioequivalence: A rational bioavailability evaluation approach on account of the pharmaceutical-driven balance of population average and variability.CPT Pharmacometrics Syst Pharmacol. 2022 Apr;11(4):482-493. doi: 10.1002/psp4.12775. Epub 2022 Mar 18. CPT Pharmacometrics Syst Pharmacol. 2022. PMID: 35303757 Free PMC article.
-
Biometrical evaluation of bioequivalence trials using a bootstrap individual direct curve comparison method.Eur J Drug Metab Pharmacokinet. 2002 Jan-Mar;27(1):11-6. doi: 10.1007/BF03190400. Eur J Drug Metab Pharmacokinet. 2002. PMID: 11996322
-
Bioequivalence evaluation of two 5% ceftiofur hydrochloride sterile suspension in pigs.J Vet Med Sci. 2018 Dec 11;80(12):1847-1852. doi: 10.1292/jvms.18-0470. Epub 2018 Nov 1. J Vet Med Sci. 2018. PMID: 30381675 Free PMC article. Clinical Trial.
-
Dissolution comparisons using a Multivariate Statistical Distance (MSD) test and a comparison of various approaches for calculating the measurements of dissolution profile comparison.AAPS J. 2017 Jul;19(4):1091-1101. doi: 10.1208/s12248-017-0063-y. Epub 2017 Mar 28. AAPS J. 2017. PMID: 28353216
-
Challenges in Permeability Assessment for Oral Drug Product Development.Pharmaceutics. 2023 Sep 28;15(10):2397. doi: 10.3390/pharmaceutics15102397. Pharmaceutics. 2023. PMID: 37896157 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources