Literature DB >> 12865037

Sample size calculation for bioequivalence studies with high-order crossover designs.

Roger P Qu, Hongjie Zheng.   

Abstract

Mesh：

Year:  2003        PMID： 12865037     DOI： 10.1016/s0197-2456(02)00317-3

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN： 0197-2456


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  2 in total

1.  Acceptability of different oral formulations in infants and preschool children.

Authors:  Diana A van Riet-Nales; Barbara J de Neef; Alfred F A M Schobben; José A Ferreira; Toine C G Egberts; Catharine M A Rademaker
Journal:  Arch Dis Child       Date:  2013-07-13       Impact factor: 3.791

2.  Relative Bioavailabilities of Lisdexamfetamine Dimesylate and D-Amphetamine in Healthy Adults in an Open-Label, Randomized, Crossover Study After Mixing Lisdexamfetamine Dimesylate With Food or Drink.

Authors:  James Ermer; Mary Corcoran; Kenneth Lasseter; Patrick T Martin
Journal:  Ther Drug Monit       Date:  2016-12       Impact factor: 3.681
  2 in total

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