Exelixis and Sairopa B.V. announced that the FDA has cleared Sairopa’s investigational new drug, or IND, application to evaluate the safety and pharmacokinetics of ADU-1805 in adults with advanced solid tumors. As a monoclonal antibody active against all human alleles of SIRPa, ADU-1805 has the potential to address a broader patient population than other SIRPa-directed therapies.
Published first on TheFly
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