Panel Digital Health Technologies track
Building the Business Case for Adopting Digital Endpoints in Clinical Trials
Tue, Feb 4, 2025 · 4:50–5:25 PM EST Rosen Shingle Creek
About this session
Panel Discussion.
FDA recently qualified the first digital endpoint for clinical trials, and recent research has shown that digital endpoints can reduce the timelines and cost of clinical trials. However, to date, decision-makers have not had the clear value assessments, routine use cases, and efficient deployment strategies needed to confidently deploy digital endpoints at scale. In this session, collaborators from the Digital Medicine Society (DiMe)'s Building the Business Case for Digital Endpoints team will unveil new insights and project resources designed to shed light on the full return on investment of digital endpoints and to drive adoption in high-quality, fit-for-purpose digital measures as endpoints in clinical research. Discussion points:Learn about DiMe’s value framework for including digital endpoints in clinical research, including when and how digital endpoints can show true value during medicinal product developmentUnderstand how to measure and evaluate the return on investment generated by digital endpointsCultivate expertise towards making informed decisions and sustain investment in integrating digital endpoints into successful digital health strategies
Speakers
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Scientific Lead · Evinova An AstraZeneca Healthtech Co
Panelist
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Executive Director, Head · Kardigan Bio
Panelist