GeneDx Fuels Rare Disease Drug Discovery with Launch of GeneDx Discover
SMFR 11.19.2024

New Biopharma Solution Aims to Accelerate the Delivery of Precision Medicine to More Patients
Today’s drug discovery and development process is not scalable to meet society’s growing needs. On average, developing a new therapy costs
Genetic data is a powerful tool that can significantly enhance the therapeutic development process, including reducing costs, accelerating timelines, and increasing success rates1. With access to genetic diagnoses continuing to expand, the impact of genetics on therapeutic development is growing. With more than 700,000 clinical exomes and genomes, GeneDx’s industry leading dataset is one of the most sophisticated in the industry and can now be leveraged as a solution for biopharmaceutical companies to drive evidence-based decision making and accelerate the development of new treatments.
"With nearly 25 years of expertise in clinical genetic data,
GeneDx Discover is a self-service tool which leverages real-world data to enable a deeper understanding of the characteristics of target patient populations. The easy-to-use tool combines disease prevalence and phenotypic information, alongside variant-level details, unlocking a deeper understanding of the size and unique characteristics of the total addressable market for genetically-defined disease cohorts, and obtaining variant-level resolution to define the cohort. Through GeneDx Discover, partners have access to demographics, geographic disease distribution, variant information and the ability to filter searches by Human Phenotype Ontology (HPO) to refine cohorts based on specific phenotypic features.
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Through its various partnerships,
About
References: |
1Minikel, E.V., Painter, J.L., Dong, C.C.et al.Refining the impact of genetic evidence on clinical success.Nature629, 624–629 (2024) |
2Paul, S., Mytelka, D., Dunwiddie, C.et al.How to improve R&D productivity: the pharmaceutical industry's grand challenge.Nat Rev Drug Discov9, 203–214 (2010) |
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