FilingSEC EDGAR8-K
Prelude Therapeutics Receives FDA Clearance for Phase 1 Study of PRT13722
· SEC accepted
StagePhase 1
Filing content
Prelude Therapeutics received FDA clearance for its IND application to initiate a Phase 1 study of PRT13722 in patients with HR+/HER2- breast cancer, with enrollment expected to begin in the fourth quarter of 2026.
AI summary of the filing. Please also check the source.Analyzed by WAPE AI.
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