Action required: Please refresh your browser
We have recently implemented some changes that require a hard refresh of your browser: Please hold down the CTRL-key and press the F5 key.
After a successful hard refresh, this message should not appear anymore.
More details about this topic are available here »
The Guardant360® Assay Receives Expedited Access Pathway Designation for Breakthrough Devices from FDA | ||
By: PR Newswire Association LLC. - 15 Feb 2018 | Back to overview list |
|
REDWOOD CITY, Calif., Feb. 15, 2018 /PRNewswire/ -- The Guardant360® assay, the leading comprehensive liquid biopsy, received an Expedited Access Pathway (EAP) designation from the United States Food and Drug Administration, Guardant Health announced. If approved, the Guardant360 assay could be the first FDA-approved comprehensive liquid biopsy. "This marks a critical milestone for our work with the FDA, and an important moment in the development of comprehensive liquid biopsies," said Guardant Health Co-Founder and President AmirAli Talasaz. "This designation allows us to work hand in hand with the FDA as we prepare our submission to the FDA later this year. Accomplishing this goal will be critical as we deepen our capabilities for our partners in the biopharma industry." Guardant360 is a comprehensive liquid biopsy that helps oncologists select the optimal treatment for advanced cancer patients without the need for an invasive tissue biopsy. Guardant360 has been extensively validated and is supported by more than 20 clinical outcome studies. It is available in more than 30 countries. The Expedited Access Pathway is intended to speed review of breakthrough technologies and medical devices that serve unmet medical needs. Through the program, the FDA will work with Guardant Health to finalize its data development plan, providing access to senior FDA officials and facilitating a collaborative, cross-disciplinary review. The FDA is expected to replace the EAP soon with its new Breakthrough Devices Program. Premarket Approval Applications from EAP-designated devices typically receive priority review at the FDA, and all submissions designated as Breakthrough Devices are set to receive priority review. "Our FDA submission for Guardant360 is Guardant Health's top priority for 2018," said Guardant Health Co-Founder and CEO Helmy Eltoukhy. "The ability to tap into the FDA's expertise and support will be invaluable as we work toward our goal of seeking the first FDA approval for a comprehensive liquid biopsy." About Guardant Health
View original content:http://www.prnewswire.com/news-releases/the-guardant360-assay-receives-expedited-access-pathway-designation-for-breakthrough-devices-from-fda-300599629.html SOURCE Guardant Health |
||
|
||
Copyright 2018 PR Newswire Association LLC. | Back to overview list |