Additional results for 'Sequential design approaches for bioequivalence studies with crossover designs'

Pharmaceutical Statistics

Volumn 11, Issue 1, 2012, Pages 8-13

  Montague, Timothy H ^a   Potvin, Diane ^b   Diliberti, Charles E ^c   Hauck, Walter W ^d   Parr, Alan F ^a   Schuirmann, Donald J ^e  

^a GLAXOSMITHKLINE   (United States)

^b INSTITUTE FOR RESEARCH IN IMMUNOLOGY AND CANCER   (Canada)

^c Montclair Bioequivalence Services   (United States)

^d UNITED STATES PHARMACOPEIA   (United States)

^e CENTER FOR DRUG EVALUATION AND RESEARCH   (United States)

Author keywords

adaptive design; bioequivalence; sample size re estimation; sequential design

Indexed keywords

BIOEQUIVALENCE; CROSSOVER PROCEDURE; ERROR; REVIEW; SEQUENTIAL ANALYSIS;

CROSS-OVER STUDIES; HUMANS; PHARMACEUTICAL PREPARATIONS; RESEARCH DESIGN; THERAPEUTIC EQUIVALENCY;

EID: 84856554236     PISSN: 15391604     EISSN: 15391612     Source Type: Journal    
DOI: 10.1002/pst.483     Document Type: Review

References (2)

1. Potvin D, DiLiberti CE, Hauck WW, Parr AF, Schuirmann DJ, Smith RA,. Sequential design approaches for bioequivalence studies with crossover designs. Pharmaceutical Statistics 2008; 7: 245-262.
2. Pocock SJ,. Group sequential methods in the design and analysis of clinical trials. Biometrika 1977; 64: 191-199. (Pubitemid 8145484)