Guardant Health Collaborated with AnHeart Therapeutics to Develop Guardant360 CDx and Guardant360 TissueNext for Taletrectinib
- The companies collaborated for the development, regulatory approval & commercialization of Guardant360 CDx & Guardant360 TissueNext assays as CDx for taletrectinib in the US & EU
- The focus of the collaboration is on the use of the Guardant tests for genomic profiling to identify patients who have the particular tumor mutations targeted by taletrectinib
- Taletrectinib (ROS1 inhibitor) received the BTD from the US FDA on Aug 2022 for advanced or metastatic ROS1+ NSCLC. The results showed excellent potency against crizotinib resistance, good brain penetration & intracranial antitumor activity, and favorable safety profiles in ROS1 fusion-positive NSCLC patients with few neurological adverse events
Ref: Businesswire | Image: Guardant Health
Related News:- Guardant Health Receives the US FDA’s Approval of Guardant360 CDx Liquid Biopsy Test for Breast Cancer
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