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Conclusion: We have discovered a novel liver targeted oral PD-L1 small molecule inhibitor, ALG-094103, with similar in vitro potency to ALG-093702 and INCB08655, and with significantly improved oral bioavailability

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553,632 A moderately toxic dose of APAP enhances liver regeneration by promoting -catenin nuclear translocation, while a severe overdose suppresses -catenin binding to the Ccnd1 promoter

Standard cycling protocols (4-8 weeks on, 2-4 weeks off) further minimize any theoretical dependence risk

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