On estimands and the analysis of adverse events in the presence of varying follow‐up times within the benefit assessment of therapies

Author:

Unkel Steffen1ORCID,Amiri Marjan2,Benda Norbert3ORCID,Beyersmann Jan4,Knoerzer Dietrich5,Kupas Katrin6,Langer Frank7,Leverkus Friedhelm8,Loos Anja9,Ose Claudia2,Proctor Tanja10,Schmoor Claudia11,Schwenke Carsten12,Skipka Guido13,Unnebrink Kristina14,Voss Florian15,Friede Tim1ORCID

Affiliation:

1. Department of Medical StatisticsUniversity Medical Center Goettingen Goettingen Germany

2. Center for Clinical TrialsUniversity Hospital Essen Essen Germany

3. Biostatistics and Special Pharmacokinetics Unit, Federal Institute for Drugs and Medical Devices Bonn Germany

4. Institute of StatisticsUlm University Germany

5. Roche Pharma AG Grenzach Germany

6. Bristol‐Myers Squibb GmbH & Co. KGaA München Germany

7. Lilly Deutschland GmbH Bad Homburg Germany

8. Pfizer Deutschland GmbH Berlin Germany

9. Merck KGaA Darmstadt Germany

10. Institute of Medical Biometry and InformaticsUniversity of Heidelberg Heidelberg Germany

11. Clinical Trials Unit, Faculty of Medicine and Medical CenterUniversity of Freiburg Freiburg im Breisgau Germany

12. Schwenke Consulting: Strategies and Solutions in Statistics (SCO:SSIS) Berlin Germany

13. Institute for Quality and Efficiency in Health Care Cologne Germany

14. AbbVie Deutschland GmbH & Co. KG Ludwigshafen Germany

15. Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Germany

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Reference74 articles.

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