1. Hasselt University, Center for Statistics, Diepenbeek, Belgium;2. International Drug Development Institute, Ottignies Louvain-la-Neuve, Belgium
Abstract:
For a number of reasons, surrogate endpoints are considered instead of the so-called true endpoint in clinical studies, especially when such endpoints can be measured earlier, and/or with less burden for patient and experimenter. Surrogate endpoints may occur more frequently than their standard counterparts. For these reasons, it is not surprising that the use of surrogate endpoints in clinical practice is increasing.