Sep, 2024
HANGZHOU, China, September 12, 2024 – The recombinant humanized anti-EGFR-CD3 enzyme-controlled bispecific antibody (hereinafter referred to as CMDE005), developed by Centrymed based on its proprietary dual-antibody platform, proBiTE, has been approved for clinical trials by the NMPA for the treatment of various EGFR-positive advanced solid tumors.
As the pharmaceutical research collaborator for the IND application of the CMDE005 project, HJB extends warm congratulations on the approval of this project for clinical trials.