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recently,, Yimin Angko Bio
Pharmaceutical(http://Technology (Shanghai) LimitedCompany
(http://("Yimin Angko"), announced that the company's new generation of immunocheckpoint inhibitors (item number: IMM01) has been granted the clinicaltesting(http://license of the NationalMedicines(http://Regulatory Authority (NMPA) (http:// for the treatment of cancer(The IMM01 project for injection is based on a new generation of immuno-checkpoint inhibitors with independent intellectual property rights developed on the yimin Angko "mAb-Trap" technology platform, and plays a powerful tumor immunotherapy effect by activating the phagocytophated phagocytosis of macrophages to the phagocytosis of tumor cellspreclinical research data confirm edi-IMM01 has achieved remarkable therapeutic results in a variety of tumor models, and because IMM01 does not bind to human red blood cells, it has obvious advantages in safetyIt is reported that YiMingAngko submitted IND to the State Drug Administration (NMPA) on March 18, 2019, and on May 14, 2019, approved the clinical I/II trial research license, which took only 39 working days from acceptance to approvalYiminenko submits the IND to theFDA(http://the approval of this project marks the entry of the first CD47 fusion proteindrug(http://research in China authorized by Yimin Angke to obtainPatent(http://independent research and development