Create an account

Already have an account?
Technical support
Send
The password is: uppercase and lowercase English letters and numbers, no less than 6 characters
Submit

Login

Don’t have an account? Sign up
Forgot password?
Login
AmoyDx ROS1 Gene Fusions Detection Kit was Approved by South Korea MFDS as Companion Diagnostics for Pfizer's Crizotinib
Back

October 1, 2018–Amoy Diagnostics of Xiamen, China today announced that it has received regulatory approval from South Korea's Ministry of Food and Drug Safety (MFDS) for its ROS1 fusion PCR assay as a companion diagnostics for Pfizer's ROS1 inhibitor Xalkori (Crizotinib).

AmoyDx ROS1gene fusions detection kit is approved asAmoyDx ROS1 Gene Fusions Detection Kitby Clinomics Inc. (AmoyDx’s Distributor in South Korea), to identify advanced non-small cell lung cancer (NSCLC) patients who habor ROS1 gene fusion and therefore might benefit from crizotinib. ROS1 gene rearrangements occur in about 2.4% of Asian patients with NSCLC. An estimated 1.5 million new cases of NSCLC are diagnosed worldwide each year.
AmoyDx ROS1 fusion kit detects 14 ROS1 gene fusions, which uses RT-PCR technology to analyze tumor messenger RNA from human tumor tissue or body fluids, and can provide results within 2.5 hours on most commercially available real-time PCR instruments. The kit has also obtained CE mark in 2013 and Chinese NMPA approval in 2014.
The MFDS’s approval of companion diagnostics is based on the data from the clinical study used to support the approval. Phase II Study of Crizotinib in East Asian had shown durable responses in 127 patients with ALK-negative and ROS1-positive metastatic NSCLC. The patients’ ROS1 status were determined using AmoyDx RT-PCR assay. The response rate on independent review was 71.7% (95% CI, 63.0% to 79.3%), with a median progression-free survival of 15.9 months*.
 
*Phase II Study of Crizotinib in East Asian Patients With ROS1-Positive Advanced Non–Small-Cell Lung Cancer

 

About AmoyDx

Amoy Diagnostics Co., Ltd. (AmoyDx) focuses on molecular diagnostics for oncology precision medicine. With completely independent intellectual property rights of ADx-ARMS and Super-ARMS technologies, AmoyDx has a market-leading portfolio of molecular diagnostic kits including but not limited to EGFR, RAS, ALK, BRAF, PIK3CA and ROS1 testing kit, which were firstly approved by CFDA and CE certified.
In European EMQN and Chinese PQCC programs, AmoyDx is the NO.1 testing kits supplier for some years and always achieves the highest accuracy rate. Nowadays AmoyDx serves an extensive domestic and international oncology network reaching over 300 hospitals in China and 50 countries all over the world. Every year hundreds of thousands of cancer patients are benefitted from AmoyDx products. AmoyDx is strategic partner of AstraZeneca, Boehringer-Ingelheim, Pfizer, Merck and Illumina, providing diagnostic products and services for medicine development and clinical studies in gene tissue and blood testing. AmoyDx ROS1 kit was recently approved by Japanese authority PMDA as the sole companion diagnostic kit for Pfizer’s crizotinib, which became the 1st approved CDx kit in the world for lung cancer patients’ ROS1 testing.

 

About Clinomics Inc.

Clinomics Co., Ltd is established in 2011 with the vision of the world's leading provider of personalized healthcare, focuses on the commercialization of next generation Precision Diagnostics/Medicine products.

Amoy Diagnostics achieved China NMPA Approval of Multi-Genes Mutations Detection Kit

Next

Subscribe
to our
newsletter

Subscribe to our newsletter

Subscribe Now