Country for PR: Hong Kong
Contributor: PR Newswire Asia (Hong Kong)
Wednesday, February 03 2021 - 21:41
AsiaNet
Guardant360 CDx submitted for regulatory approval in Japan
TOKYO, Feb. 3, 2021 /PRNewswire-AsiaNet/ --

A comprehensive genomic profiling test utilizing blood samples from patients 
with advanced solid tumors  

Guardant Health Japan, an affiliate of Guardant Health Asia, Middle East & 
Africa (AMEA) has announced that it has submitted its application to the 
Ministry of Health, Labour and Welfare (MHLW) for regulatory approval of 
Guardant360 CDx, a liquid biopsy test for tumor mutation profiling, also known 
as comprehensive genomic profiling (CGP) in patients with advanced solid 
cancerous tumors.
 
"I am delighted to announce that we have submitted the regulatory application 
for Guardant360 CDx liquid biopsy test for approval by MHLW. Several clinical 
studies1,2 have shown that compared to invasive tissue-based testing, 
Guardant360 has a quicker turnaround time for reporting comprehensive genomic 
test results. For the patient, this means a shorter waiting time to get the 
most appropriate treatment while avoiding safety risks related to tissue 
biopsies. We are excited to make this a possibility in clinical practice for 
cancer patients in Japan," said Simranjit Singh, Chief Executive Officer of 
Guardant Health AMEA & Representative Director of Guardant Health Japan.

Guardant360 CDx is a liquid biopsy test that analyzes circulating tumor DNA 
(ctDNA) from the blood samples of patients with advanced solid tumors and 
identifies genetic alterations that may inform treatment decisions. In addition 
to the submission of Guardant360 CDx for tumor mutation profiling, Guardant 
Health Japan has simultaneously filed for a Companion Diagnostic (CDx) 
approval. On August 7, 2020, the U.S. Food and Drug Administration (FDA) 
approved the Guardant360(R)CDx for comprehensive genomic profiling across all 
solid cancers and as a companion diagnostic to identify non-small cell lung 
cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) 
alterations who may benefit from treatment with Tagrisso(R)(osimertinib). This 
approval represented the first FDA-approved liquid biopsy test for  
comprehensive tumor mutation profiling across all solid cancers. 

Guardant Health Japan aims to contribute to precision oncology in Japan by 
supporting research and development efforts and drive broad clinical adoption 
of Guardant Health's products.
 
About Guardant Health Japan 

Guardant Health Japan is an affiliate of Guardant Health AMEA, Inc., a joint 
venture between SoftBank and Guardant Health, Inc., a leading precision 
oncology company focused on helping conquer cancer globally through use of its 
proprietary blood tests, vast data sets and advanced analytics.

References

1. Leighl NB, Page RD, Raymond, VM, et al. Clinical Utility of Comprehensive 
Cell-Free DNA Analysis to Identify Genomic Biomarkers in Patients with Newly 
Diagnosed Metastatic Non-Small Cell Lung Cancer, Clin Cancer Res. doi: 
10.1158/1078-0432.CCR-19-0624.

2. Nakamura, Y., Taniguchi, H., Ikeda, M. et al. Clinical utility of 
circulating tumor DNA sequencing in advanced gastrointestinal cancer: 
SCRUM-Japan GI-SCREEN and GOZILA studies. Nat Medicine (2020). 
https://doi.org/10.1038/s41591-020-1063-5 



SOURCE Guardant Health
Translations

Japanese