STATISTICAL METHODS FOR TWO-SEQUENCE THR
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SHEIN-CHUNG CHOW; JUN SHAO
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Article
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1997
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John Wiley and Sons
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English
⚖ 211 KB
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In clinical trials, and in bioavailability and bioequivalence studies, one often encounters replicate cross-over designs such as a two-sequence three-period cross-over design to assess treatment and carry-over effects of two formulations of a drug product. Because of the potential dropout (or for so