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Inflation of Type I Error in the Evaluation of Scaled Average Bioequivalence, and a Method for its Control.

Detlew LabesHelmut Schütz
Published in: Pharmaceutical research (2016)
Applying the European Medicines Agency's ABEL method at the nominal level of 0.05 inflates the type I error to an unacceptable degree, especially close to a CV wR of 30%. To control the type I error nominal levels ≤0.05 should be employed. Iteratively adjusting α is suggested to find optimal levels of the test.
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