In parallel, γ-H2A.X levels were significantly increased by fadraciclib monotherapy (50 mg/kg) and showed an increasing trend with the fadraciclib-olaparib combination, indicating DNA damage.
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Fadraciclib, a CDK2/CDK9 inhibitor, shows efficacy in biliary tract cancer and synergistic potential with olaparib and JQ1 based on MCL1 expression.
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