References for trial designs [Design Issues]

posted by Helmut Homepage – Vienna, Austria, 2007-04-03 14:26 (5574 d 04:38 ago) – Posting: # 615
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Dear Rahul,

just a list of textbooks published within the last ten years:
  1. Hauschke D, Steinijans V, Pigeot I. Bioequivalence Studies in Drug Development. Chichester: Wiley; 2007.
  2. Patterson S, Jones B. Bioequivalence and Statistics in Clinical Pharmacology. Boca Raton: Chapman & Hall/CRC; 2006.
  3. Matthews JNS. Introduction to Randomized Controlled Clinical Trials. Boca Raton; Chapman & Hall/CRC: 2nd ed. 2006.
  4. Senn S. Statistical Issues in Drug Development. Chichester; Wiley: 1997, reprint with corrections 2004.
  5. Bolton S, Bon C. Pharmaceutical Statistics. New York; Marcel Dekker: 4th ed. 2004.
  6. Jones B, Kenward MG. Design and Analysis of Cross-over Trials. Boca Raton; Chapman & Hall/CRC: 2nd ed. 2003.
  7. Wellek S. Testing Statistical Hypotheses of Equivalence. Boca Raton; Chapman & Hall/CRC: 2003.
  8. Senn S. Cross-over Trials in Clinical Research. Chichester; Wiley: 2nd ed. 2002.
  9. Millard SP, Krause A, editors. Applied Statistics in the Pharmaceutical Industry. New York; Springer: 2001.
  10. Chow S-C, Liu J-p. Design and Analysis of Bioavailability and Bioequivalence Studies. New York; Marcel Dekker: 2nd ed. 2000.
  11. Chow S-C, Liu J-p. Design and Analysis of Clinical Trials. Chichester; Wiley: 1998.
Textbooks given above are more or less leaning towards statistics.

A more guideline-driven overview of approaches is given byOf course, you will need some background in PK/PD and NCA as well, e.g.,
  1. Gibaldi M, Perrier D. Pharmacokinetics. New York; Marcel Dekker: 3rd ed. 2006.
  2. Gabrielsson J, Weiner D. Pharmacokinetic an Pharmacodynamic Data Analysis: Concepts and Applications. Stockholm: Swedish Pharmaceutical Press; 3rd ed. 2000.
  3. Cawello W, editor. Parameters for Compartment-Free Pharmacokinetics. Aachen: Shaker-Verlag; 2003.

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