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- W1978379059 abstract "Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing prednisone are reviewed. Due to insufficient data prednisone cannot be definitively classified according to the current Biopharmaceutics Classification System (BCS) criteria as both the solubility and the permeability of prednisone are on the borderline of the present criteria of BCS Class I. Prednisone's therapeutic indications and therapeutic index, pharmacokinetics and the possibility of excipient interactions were also taken into consideration. Available evidence indicates that a biowaiver for IR solid oral dosage forms formulated with the excipients tabulated in this article would be unlikely to expose patients to undue risks." @default.
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- W1978379059 date "2007-06-01" @default.
- W1978379059 modified "2023-10-10" @default.
- W1978379059 title "Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Prednisone" @default.
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- W1978379059 doi "https://doi.org/10.1002/jps.20817" @default.
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