Recurrent events in clinical trials



Tobias Mütze, Novartis Pharma AG

Antje Jahn, Darmstadt University of Applied Sciences

Benjamin Hofner, Paul-Ehrlich-Institut

Day: Sunday, September 6

Length of tutorial: half day

Technical level: low


In this tutorial, participants have the opportunity to get an overview of common models for recurrent event endpoints in clinical trials, to learn about their strengths and shortcomings, and how to fit these models in R. Accomplished by the presentation of real life examples and regulatory considerations, the tutorial will enhance the participants skills in planning, analyzing, and interpreting clinical trials with recurrent event data.

Local Organizer:

Institute of Biometry and Clinical Epidemiology
Charité - Universitätsmedizin Berlin & Berlin Institute of Health