Literature DB >> 28155028

The Two Main Goals of Bioequivalence Studies.

Laszlo Endrenyi1, Henning H Blume2, Laszlo Tothfalusi3.   

Abstract

The principal goal of bioequivalence (BE) investigations has crucial importance and has been the subject of extensive discussions. BE studies are frequently considered to serve as procedures for sensitive discrimination. The BE investigation should be able to provide methods and conditions sensitively identifying relevant differences between drug products if such differences in fact exist. Alternatively, BE studies can be deemed as surrogates of clinical investigations assessing therapeutic equivalence. Bioequivalent drug products will be provided to patients for their benefits. Both points of view are valid since they represent two aspects of product performance. It has been argued that both should be equally sustained and applied. In practice, however, they collide when regulatory conditions and statements are developed. For instance, some regulators prefer to conduct BE studies following single drug administrations since these conditions are considered to provide the highest sensitivity of discrimination between pharmacokinetic profiles and thus, a product's in-vivo performance. Others suggest that, at least for modified-release products, BE investigations should be performed in the steady state since it represents clinical conditions. Preference for one point of view or the other pervades other regulatory statements including suggestions for subjects to be selected in studies and pharmacokinetic measures to be evaluated. An overview is provided on the disturbing inconsistency of statements within and between regulations. It is argued that harmonization would be highly desirable, and relevant recommendations are offered.

Entities:  

Keywords:  bioequivalence; clinical surrogate; product performance; regulatory expectations; sensitive discrimination

Mesh:

Year:  2017        PMID: 28155028     DOI: 10.1208/s12248-017-0048-x

Source DB:  PubMed          Journal:  AAPS J        ISSN: 1550-7416            Impact factor:   4.009


  34 in total

Review 1.  The role of metabolites in bioequivalence.

Authors:  Kamal K Midha; Maureen J Rawson; John W Hubbard
Journal:  Pharm Res       Date:  2004-08       Impact factor: 4.200

2.  Bioequivalence of highly variable drugs: a comparison of the newly proposed regulatory approaches by FDA and EMA.

Authors:  Vangelis Karalis; Mira Symillides; Panos Macheras
Journal:  Pharm Res       Date:  2011-12-28       Impact factor: 4.200

3.  Absorption rate vs. exposure: which is more useful for bioequivalence testing?

Authors:  T N Tozer; F Y Bois; W W Hauck; M L Chen; R L Williams
Journal:  Pharm Res       Date:  1996-03       Impact factor: 4.200

4.  Is Cmax/AUC useful for bioequivalence testing?

Authors:  A Rostami-Hodjegan; G T Tucker
Journal:  J Pharm Sci       Date:  1997-12       Impact factor: 3.534

5.  Secondary metrics for the assessment of bioequivalence.

Authors:  L Endrenyi; L Tothfalusi
Journal:  J Pharm Sci       Date:  1997-03       Impact factor: 3.534

6.  Use of partial area under the curve metrics to assess bioequivalence of methylphenidate multiphasic modified release formulations.

Authors:  Ethan M Stier; Barbara M Davit; Parthapratim Chandaroy; Mei-Ling Chen; Jeanne Fourie-Zirkelbach; Andre Jackson; Stephanie Kim; Robert Lionberger; Mehul Mehta; Ramana S Uppoor; Yaning Wang; Lawrence Yu; Dale P Conner
Journal:  AAPS J       Date:  2012-09-14       Impact factor: 4.009

7.  Evaluation of different indirect measures of rate of drug absorption in comparative pharmacokinetic studies.

Authors:  L F Lacey; O N Keene; C Duquesnoy; A Bye
Journal:  J Pharm Sci       Date:  1994-02       Impact factor: 3.534

8.  Bio-International 92, conference on bioavailability, bioequivalence, and pharmacokinetic studies.

Authors:  H H Blume; K K Midha
Journal:  J Pharm Sci       Date:  1993-11       Impact factor: 3.534

9.  Regulatory and study conditions for the determination of bioequivalence of highly variable drugs.

Authors:  Laszlo Endrenyi; Laszlo Tothfalusi
Journal:  J Pharm Pharm Sci       Date:  2009       Impact factor: 2.327

10.  Analysis of Intra- and Intersubject Variability in Oral Drug Absorption in Human Bioequivalence Studies of 113 Generic Products.

Authors:  Masahisa Sugihara; Susumu Takeuchi; Masaru Sugita; Kazutaka Higaki; Makoto Kataoka; Shinji Yamashita
Journal:  Mol Pharm       Date:  2015-11-20       Impact factor: 4.939

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  2 in total

1.  Bioequivalence and Therapeutic Equivalence of Generic and Brand Bupropion in Adults With Major Depression: A Randomized Clinical Trial.

Authors:  Evan D Kharasch; Alicia Neiner; Kristin Kraus; Jane Blood; Angela Stevens; Julia Schweiger; J Philip Miller; Eric J Lenze
Journal:  Clin Pharmacol Ther       Date:  2019-01-18       Impact factor: 6.875

Review 2.  The use of GA-RxODE (Genetics Algorithms and Running simulations from Ordinary Differential Equations-based model) method to optimize bioequivalence studies.

Authors:  Ezequiel Omar Nuske; Mikhail Morozov; Héctor Alejandro Serra
Journal:  Pharmacol Res Perspect       Date:  2021-10
  2 in total

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