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Is the time to progression ratio an appropriate endpoint for clinical trials? A critical examination of current practice and suggestions for a new methodology
- Source :
- 65th Annual Meeting of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS), Meeting of the Central European Network (CEN: German Region, Austro-Swiss Region and Polish Region) of the International Biometric Society (IBS); 20200906-20200909; Berlin; DOCAbstr. 288 /20210226/
- Publication Year :
- 2021
- Publisher :
- German Medical Science GMS Publishing House; Düsseldorf, 2021.
-
Abstract
- Background: The time to progression ratio (TTPr) is a novel endpoint in Phase I/II oncology trials, which is frequently applied to evaluate the efficacy of molecular targeted treatments in late stage patients. The general idea of the design is that a patient serves as their own control. To[for full text, please go to the a.m. URL]<br />65th Annual Meeting of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS), Meeting of the Central European Network (CEN: German Region, Austro-Swiss Region and Polish Region) of the International Biometric Society (IBS)
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- 65th Annual Meeting of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS), Meeting of the Central European Network (CEN: German Region, Austro-Swiss Region and Polish Region) of the International Biometric Society (IBS); 20200906-20200909; Berlin; DOCAbstr. 288 /20210226/
- Accession number :
- edsair.doi.dedup.....ec9123d5a18ea847e55c3211c9b1349a