Developing and validating robust and sensitive biomarkers early in the oncology drug development process is key to progressing personalized medicine, as well as improving anticancer agent attrition rates. Clinical testing of these biomarkers, and associated CDx, is also facilitated, ultimately de-risking clinical trials.
This White Paper presents three biomarker discovery and validation strategies in early-stage oncology drug development through a systems biology approach. How to use translational preclinical models to identify and use biomarkers is highlighted, alongside methods to transfer preclinical biomarkers to the clinical space.
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2024-10-16
2020-01-28
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