A comparison of the Two One-Sided Tests Procedure and the Power Approach for assessing the equivalence of average bioavailability
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics
Link
http://link.springer.com/content/pdf/10.1007/BF01068419.pdf
Reference7 articles.
1. W. W. Hauck and S. Anderson. A new statistical procedure for testing equivalence in two-group comparative bioavailability trials.J. Pharmacokin. Biopharm. 12:83–91 (1984).
2. W. J. Westlake. Response to T. B. L. Kirkwood: Bioequivalence testing-a need to rethink.Biometrics 37:589–594 (1981).
3. S. Anderson and W. W. Hauck. A new procedure for testing equivalence in comparative bioavailability and other clinical trials.Comm. Stat. A 12:2663–2692 (1983).
4. D. M. Rocke. On testing for bioequivalence.Biometrics 40:225–230 (1984). (See also Correspondence inBiometrics 4:561–563 (1985).)
5. W. J. Westlake. The design and analysis of comparative blood-level trials. In J. Swarbrick (ed.),Current Concepts in the Pharmaceutical Sciences, Dosage Form Design and Bioavailability, Lea and Febiger, Philadelphia, 1973, pp. 149–179.
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