Guardant Health Receives Regulatory Approval for Guardant360 CDx in Japan

Additionally, in December 2021, MHLW granted regulatory approval of the Guardant360 CDx liquid biopsy test as a companion diagnostic for identifying patients with metastatic non-small cell lung cancer (NSCLC) who may benefit from treatment with LUMAKRAS™ (sotorasib), a KRAS G12C inhibitor developed and manufactured by Amgen.

“We are delighted to receive regulatory approval in Japan for the Guardant360 CDx test. We strongly believe that our liquid biopsy test will help to enhance the quality of cancer management in Japan by offering tumor mutation profiling and companion diagnostics for therapies in patients whose tumors have KRAS G12C or MSI-High status. One of the key benefits of our liquid biopsy test is that it enables physicians to match patients to appropriate treatment quickly without the complications and delays of a tissue biopsy,” said Simranjit Singh, Chief Executive Officer of Guardant Health AMEA and Representative Director of Guardant Health Japan.

“Guardant Health Japan is dedicated to bringing innovative and comprehensive liquid biopsy tests such as Guardant360 CDx to Japan so that patients with advanced stage cancer can benefit from genomic profiling information. This regulatory approval has been made possible because of the collaborations we have with leading cancer experts in Japan. We are strongly committed to serving Japanese patients and physicians, and this is the first of many products in the Guardant portfolio which we plan to roll out in the near future,” said Gen Asano, General Manager of Guardant Health Japan.

With just a simple blood draw from the patient, the Guardant360 CDx test helps guide treatment decisions for patients with advanced stage cancer. Having secured this regulatory approval, Guardant Health Japan aims to drive clinical adoption of liquid biopsy testing in Japan and enable more patients to receive potentially life-changing precision medicines.

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