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  • Prelude announces a clinical trial collaboration and supply agreement with Lilly to evaluate the selective KAT6A degrader PRT13722 combined with Verzenio and Inluriyo in patients with HR-positive/HER2-negative breast cancerOct 13, 2026
  • FDA cleared Prelude Therapeutics' IND application for PRT13722, a first-in-class oral selective KAT6A degraderSep 10, 2026

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