adaptIVPT
Adaptive Bioequivalence Design for In-Vitro Permeation Tests
Description
Contains functions carrying out adaptive procedures using mixed scaling approach to establish bioequivalence for in-vitro permeation test (IVPT) data. Currently, the package provides procedures based on parallel replicate design and balanced data, according to the U.S. Food and Drug Administration's "Draft Guidance on Acyclovir" <https://www.accessdata.fda.gov/drugsatfda_docs/psg/Acyclovir_topical%20cream_RLD%2021478_RV12-16.pdf>. Potvin et al. (2008) <doi:10.1002/pst.294> provides the basis for our adaptive design (see Method B). For a comprehensive overview of the method, refer to Lim et al. (2023) <doi:10.1002/pst.2333>. This package reflects the views of the authors and should not be construed to represent the views or policies of the U.S. Food and Drug Administration.
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| r-oldrel-windows-x86_64 | OK |
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Changelog
Full NEWS →v1.1.0
+
msabe+
rss+
prms+
PRsurfaceCurrently, only supporting balanced data and parallel replicate design.
New features
+ The first version of adaptIVPT providing functions that help design and analyze IVPT studies.