Free Access
Med Sci (Paris)
Volume 20, Number 2, Février 2004
Page(s) 231 - 235
Section Dossier technique
Published online 15 February 2004
  1. Huguier M, Flahault A. Biostatistiques au quotidien. Paris : Elsevier, 2003 : 206 p. [Google Scholar]
  2. Pocock SJ, Geller N, Tsiatis A. The analysis of multiple endpoints in clinical trials. Biometrics 1987; 43 : 487–98. [Google Scholar]
  3. Bauer P. Multiple testing in clinical trials. Stat Med 1991; 10 : 871–90. [Google Scholar]
  4. Senn S. Statistical issues in drug development. New York : Wiley, 1997. [Google Scholar]
  5. Sankoh AJ, Huque MF, Dubey SD. Some comments on frequently used multiple endpoint adjustment methods in clinical trials. Stat Med 1997; 16 : 2529–42. [Google Scholar]
  6. Holm S. A simple sequentially rejective multiple test procedure. Scand J Stat 1979; 6 : 65–70. [Google Scholar]
  7. ICH E9. Statistical principles for clinical trials. International conference on harmonisation of technical requirements for the registration of pharmaceuticals for human use. Adopted by CPMP, juillet 2000, issued as CPMP/ICH/364/96. [Google Scholar]
  8. O’Brien P. Procedures for comparing samples with multiple endpoints. Biometrics 1984; 40 : 1079–87. [Google Scholar]
  9. Marcus R, Peritz E, Gabriel KR. On closed testing procedure with special reference to ordered analysis of variance. Biometrika 1976; 67 : 655–60. [Google Scholar]
  10. Point to consider on multiplicity issues in clinical trials. CPMP/EWP/908/99, adoption by CPMP, septembre 2002. [Google Scholar]

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