2015
January
Genetron Health Launches Oncology Diagnostics and Monitoring Platform
February
2020
January
Gene sequencer GENETRON S2000 is
approved to go to market in China
8-gene Lung
Cancer Assay is approved to go to market in China
March
Contributes to China's first 'NGS
Clinical Application Standards'
June
Research Breakthrough: For the first time,
Genetron Health reported DNA methylation data, distinct clusters termed H3-Pons, H3-Medulla, IDH, and
PA-like, each associated with unique genomic and clinical profiles. Clinical data shows significant
different overall survival between these clusters and pathway analysis demonstrates different oncogenic
mechanisms in these samples. (Nature Communications)
JUNE
Listed on Nasdaq
August
Genetron Health becomes the only company
to participate in China's Early Cancer National R&D Projects covering three different cancer varieties
(liver, lung, digestive tract)
September
Genetron Health receives U.S. FDA Breakthrough Device
designation for its blood-based NGS test, HCCscreen
November
Joined the "Liver Cancer Early Screening
Comprehensive Prevention" public health initiative
December
Genetron Health establishes various partnerships with AstraZeneca, Bayer,
CStone Pharma, Novartis, and others
2025
February
Passes CFDI Inspection, Aids in the Approval and Launch of China's First PD-1 Monoclonal Antibody for Head and Neck Squamous Cell Carcinoma
Participates in Formulating China's First National Standard for Quality Control of High-Throughput Human Gene Sequencing Data, Facilitating the Establishment of Authoritative Standards for Whole-Genome Sequencing Data
May
Participates in "National Key Science and Technology Special Projects", Leading R&D and Clinical Application of Liquid Biopsy and Big Data Technologies for Solid Tumors
Aids in Successful Approval of New Indication for HANSON PHARMA’s Lung Cancer Targeted Drug Almonertinib®
November
Genetron Health's HCCscan™, a leading early detection product for liver cancer, has been granted registration approval by the Thailand Food and Drug Administration (TFDA) under Registration No. 68-2-2-1-0010398.
Genetron Health’s blood tumor MRD product, Seq-MRD®, provided testing services for the registrational clinical trial of pCAR-19B, the first CAR-T cell therapy for pediatric leukemia approved in China. Having successfully passed the prequalification inspection by the Center for Food and Drug Inspection (CFDI) of the National Medical Products Administration (NMPA), Seq-MRD® contributed to the drug’s official approval and market launch in China.
Genetron Health’s Seq-MRD®, a blood tumor MRD detection product, supported the registrational trial of pCAR-19B, China’s first CAR T cell therapy for pediatric leukemia, enabling its NMPA approval.
December
At the global hematology conference ASH, Genetron Health’s Seq-MRD® and Onco LymScan™ drew in-depth attention from international hematology experts, drug R&D scientists, and industry partners, earning widespread acclaim.
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