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HLX97-069 is a novel, orally bioavailable small molecule inhibitor targeting lysine acetyltransferase 6A and 6B (KAT6A/B), developed by Shanghai Henlius Biotech. It is designed with a "fast-on, fast-off" pharmacokinetic profile and high selectivity to maximize anti-tumor efficacy while minimizing target-associated hematologic toxicity, such as neutropenia. In preclinical models of breast cancer, HLX97-069 demonstrated potent, dose-dependent anti-tumor activity, high oral bioavailability, and a favorable safety profile with reduced hematologic toxicity compared to other KAT6 inhibitors like PF-07248144.
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