2022

An overview on clinical endpoints and estimands framework

by cyb2025

Greta Brenna
Senior Biostatistician, PRINEOS srl, Milan

INTRODUCTION

A very crucial step in designing a clinical trial is transforming the clinical research question in the most appropriate primary endpoint. Indeed, choosing the wrong primary endpoint can lead to an unsuccessful trial.
As already stated for the sample size calculation, the endpoints definition should also be outlined at the design stage of a clinical trial and requires a close cooperation between all the stakeholders involved (e.g., clinicians, statisticians, sponsors).
This article analyzes all the main endpoint characteristics with the aim of improving awareness and understanding of their definition.

OBJECTIVE OR ENDPOINT?

The first concept to be clarified when discussing endpoints is the difference between objectives and endpoint or outcome measures.
The aim or the purpose of the study is usually defined as the primary clinical research question that the researchers are willing to investigate, that is the trial objective.

ABOUT THE AUTHOR

Greta Brenna (Senior Biostatistician, PRINEOS srl) has grown a solid experience in the field of Biostatistics applied to clinical research in contract research industries and hospital research.
She is able to understand the needs of researchers and transform them into appropriate clinical endpoints by applying the most advanced statistical methodology.
PRINEOS srl is a new strategic consulting company born and raised by passion, leveraging on a team with more than 25 years of expertise in the Life Sciences.
Our goal is to improve and innovate Clinical Research in Healthcare providing services on: Biostatistics, Medical Affairs, Regulatory and Legal Affairs.

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