Changes in circulating tumor DNA (ctDNA) levels as early as weeks after treatment initiation have been correlated with therapeutic response across multiple studies. This webinar will bring together scientific and industry leaders to examine the evolving evidence linking ctDNA dynamics to clinical outcomes and identify opportunities to strengthen the collective evidence base for ctDNA as an exploratory and potential surrogate endpoint.
Key Highlights:
- Insights from recent studies evaluating ctDNA quantitation as an indicator of therapeutic response.
- Practical applications of ctDNA for internal decision-making and dose optimization.
- Collaborative approaches to expand multi-tumor data generation and strengthen the evidence base required for endpoint qualification.
Why Attend?
- Learn more about how response monitoring with ctDNA could help to accelerate evaluation of therapy efficacy and clinical development
- Attendees can participate in a live Q&A session at the end of the presentation or submit questions in advance of the event via the registration form.
Register now to secure your spot!
Webinar Leaders
Carol Peña, PhD
Executive Director, Translational Oncology, Merck
Fernando Cruz-Guilloty, PhD
Director, Oncology – Precision Medicine & Diagnostics Lead, Johnson & Johnson
Diana Merino Vega, PhD
Senior Director, Cancer Biomarker Development, AstraZeneca
John Simmons, PhD
Global VP of Biopharma & Oncology Partnerships, Natera
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