Invitae, a leading medical genetics company, announced a partnership with BridgeBio Pharma, Inc., a commercial-stage biopharmaceutical company focused on genetic diseases and cancers, designed to advance genetics-based drug discovery for rare diseases. The goal of the collaboration is to generate new insights focused on genetic modifiers and the discovery of novel therapeutic targets for rare diseases and other unmet medical needs.
The agreement expands upon the longstanding partnership between the two companies to combine the strengths of BridgeBio’s deep expertise in rare disease research and development of therapeutics, and Invitae’s rare disease enriched dataset and analytical capabilities. Invitae has provided clinical testing for more than 4 million patients, generating an extensive dataset that is uniquely positioned to deepen insights on patients with genetic-driven disease.
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“Invitae is on a mission to bring comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. By leveraging de-identified genetic information from patients, our researchers can gain a much deeper understanding of the genetic basis of a disease,” said W. Michael Korn, M.D., chief medical officer at Invitae. “Through this partnership, we aim to support the development of novel therapeutic targets and advance transformative medicines for patients with rare disease.”
Access to large genetic and clinical datasets are needed to advance research and discover novel drug targets and are often hard to find for researchers.
“We chose to partner with Invitae because of the unique scale and depth of their dataset on affected populations. Patients with severe and highly penetrant dominant disorders are not represented in general population studies, making it nearly impossible to find data anywhere except a disease-focused cohort like Invitae’s,” said Sun-Gou Ji, Ph.D., vice president of computational genetics at BridgeBio. “These rich data sources will continue to offer researchers a mechanism to get a much deeper understanding of genetic variations and their effect on diseases.”
SOURCE : PRNewswire