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» Jacobio’s P53 Y220C activator gains FDA clearance to enter clinic for advanced solid tumors
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Cancer
Jacobio’s P53 Y220C activator gains FDA clearance to enter clinic for advanced solid tumors
March 1, 2024
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Jacobio Pharmaceuticals Group Co. Ltd. has received FDA approval of its IND application for JAB-30300, allowing it begin a phase I/IIa trial in the U.S. in advanced solid tumors.
BioWorld Science
Regulatory
Cancer
FDA
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