Country for PR: Hong Kong
Contributor: PR Newswire Asia (Hong Kong)
Saturday, August 08 2020 - 12:43
AsiaNet
First liquid biopsy to receive FDA Approval for comprehensive tumor profiling across all solid cancers, Guardant Health's Guardant360(R) CDx, gains credibility among oncologists in Asia, Middle East and Africa
SINGAPORE, Aug. 8, 2020 /PRNewswire-AsiaNet/--

The U.S. Food and Drug Administration (FDA) has approved Guardant Health's 
liquid biopsy, Guardant360(R) CDx, for tumor mutation profiling in patients 
across all solid cancers. 

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For Guardant Health Asia, Middle East and Africa (AMEA), this FDA approval 
represents a landmark achievement of the Guardant360 test. Currently, the 
liquid biopsy is commercially available in 41 countries in AMEA. For advanced 
cancer patients, this FDA approval lends even greater credibility to the test 
and its ability to provide comprehensive genomic profiling information that is 
critical to their cancer treatment. 

"This FDA approval is a significant milestone for us and it will certainly 
boost our efforts in offering Guardant360 as the preferred liquid biopsy option 
in AMEA. We remain committed to making the Guardant360 test available to as 
many advanced cancer patients as possible so that they can undergo complete 
genotyping and have the best opportunity to receive the right treatment for 
their cancer," said Mr Simranjit Singh, Chief Executive Officer of Guardant 
Health AMEA.     

"The US FDA approval validates the technology behind the Guardant360 assay that 
we offer to advanced stage cancer patients in AMEA. Treatment guidelines 
recommend testing for more than 20 different genomic biomarkers. Evaluating 
each mutation individually wastes time and delays treatment.  With Guardant360, 
physicians and patients can feel confident that relevant genes are being 
assessed with a single blood test.  Results are available within 7 days from 
receipt in the laboratory. This will help more patients start treatment sooner 
with appropriate precision cancer medicines," said Dr. Steve Olsen, Chief 
Medical Officer of Guardant Health AMEA.

Guardant Health AMEA hopes to accelerate wider adoption of 
guideline-recommended genomic profiling in clinical practice among medical 
oncologists so that advanced cancer patients in AMEA can benefit from reliable 
and comprehensive liquid biopsies such as Guardant360 and be treated quickly 
and accurately. 

About Guardant Health AMEA 

Guardant Health AMEA is a joint venture between SoftBank and Guardant Health, a 
leading precision oncology company focused on helping conquer cancer globally 
through use of its proprietary blood tests, vast data sets and advanced 
analytics. The Guardant Health oncology platform is designed to leverage its 
capabilities in technology, clinical development, regulatory and reimbursement 
to drive commercial adoption, improve patient clinical outcomes and lower 
healthcare costs. In pursuit of its goal to manage cancer across all stages of 
the disease, Guardant Health has launched multiple liquid biopsy-based tests, 
Guardant360 and GuardantOMNI, for advanced stage cancer patients, which fuel 
its LUNAR development programs for recurrence and early detection. Since its 
launch in 2014, Guardant360 has been ordered used by more than 7,000 
oncologists and over 60 biopharmaceutical companies. Visit us online at 
www.guardanthealthamea.com.

SOURCE: Guardant Health