In this free webinar, learn how genomic and real-world data can help identify and better understand rare disease patient populations across the therapy lifecycle. The featured speakers will discuss how genomic, phenotypic, claims and electronic health record data can support patient identification, trial enrollment and clinical development decisions. Attendees will also explore how insights from these data sources can inform future therapeutic development and post-approval strategies.
TORONTO, Nov. 12, 2026 /PRNewswire/ -- Understanding who the right patients are and how to find them remains a challenge across the therapy lifecycle. From clinical development and trial enrollment through post-approval, each stage generates new insights into patient populations, disease characteristics, diagnostic and healthcare journeys. This webinar explores how integrated patient data can improve patient identification and inform decisions throughout the therapy lifecycle.
Join Colleen Caleshu, MSc, LCGC, Senior Director of Translational Research, GeneDx; Joe Walter, MBA, Senior Director of Marketing, Neurvati; and Sarah Chang, PhD, Medical Strategy Lead, UCB, for the live session on Thursday, December 3, 2026, at 2pm EST / 11am PST.
This webinar brings together industry experts to examine how genomic, phenotypic, claims and electronic health record (EHR) data can help identify and better understand rare disease patient populations across the therapy lifecycle. The discussion will highlight how real-world data can identify patients who may otherwise be overlooked, support clinical development and provide insights that inform future therapeutic development programs.
The featured speakers will explore how these insights can be applied across the therapy lifecycle, drawing on large-scale, clinically derived genomic datasets containing millions of genetic tests, exome and genome sequences and phenotypic data points, complemented by claims data. Integrating these complementary data sources can strengthen the understanding of patient populations, reveal patterns in healthcare journey and support evidence-based decisions from discovery through post-approval.
Register for this webinar to learn how genomic and real-world data can improve patient population identification, support clinical development and generate insights that inform future therapeutic programs.
ABOUT GENEDX
GeneDx is a genomics pioneer with over 25 years of experience, on a mission to empower everyone to live their healthiest life through genomics. The company helps biopharma accelerate precision therapy development by connecting clinically confirmed genomic data to real-world patient outcomes. Built on ~2.5 million diagnostic tests – including more than 1 million exomes and genomes – GeneDx delivers clinical-grade genomic insights grounded in real patient care. Its dataset enables novel variant discovery, precise cohort identification, and longitudinal insights into disease progression and treatment patterns. Through direct access to over 1 million genetically defined patients and providers, GeneDx supports patient identification, trial recruitment, and engagement, turning high-confidence data into real-world impact.
To learn more about GeneDx, visit http://www.genedx.com/biopharma.
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Soumya Shashikumar
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