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» Immuneering’s IMM-6-415 receives FDA clearance for phase I/IIa trial in solid tumors with RAF or RAS mutations
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Cancer
Immuneering’s IMM-6-415 receives FDA clearance for phase I/IIa trial in solid tumors with RAF or RAS mutations
Dec. 13, 2023
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Immuneering Corp. has obtained FDA clearance of its IND application for IMM-6-415, an oral, twice-daily small molecule in development for the treatment of advanced RAF or RAS mutant solid tumors.
BioWorld Science
Regulatory
Cancer
FDA
IND