Biopharma Transcript

Prelude Therapeutics Inc PRLD

Nasdaq · Phase 1 · oncology · small molecule · EDGAR · Updated Nov 4, 2026

Prelude Therapeutics Inc (Nasdaq: PRLD) is an oncology drug developer. Its lead program, PRT12396, is in Phase 1 for polycythemia vera and myelofibrosis (JAK2V617F-mutant MPN). Its next catalyst on record is PRT13722: Phase 1 study of PRT13722 in HR+/HER2- breast cancer anticipated to begin enrolling in Q4 2026. (Q4 2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: PRT13722 — Phase 1 study of PRT13722 in HR+/HER2- breast cancer anticipated to begin enrolling in Q4 2026. (Q4 2026). 4 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
PRT12396 (JAK2V617F mutant-selective inhibitor)polycythemia vera; myelofibrosissmall moleculePhase 1
PRT13722 (KAT6A degrader)HR+/HER2- breast cancersmall moleculePre-clinical
CALR-targeted degrader antibody conjugatesmyeloproliferative neoplasmsantibodyPre-clinical
SMARCA2/4 degrader payload DACs (with AbCellera)solid tumorsantibodyPre-clinical

Recent results and decisions

  1. Sep 10, 2026
    accepted FDA cleared IND for PRT13722 Phase 1 study in HR+ breast cancer patients, with enrollment anticipated to begin in fourth quarter 2026.IND application clearance received; Phase 1 study of PRT13722 in patients with HR+/HER2- breast cancer anticipated to being enrolling in the fourth quarter. Filing
  2. Sep 10, 2026
    started Phase 1 dose escalation study of PRT13722 as monotherapy and in combinations expected to start enrolling in fourth quarter 2026.Phase 1 study of PRT13722 in patients with HR+/HER2- breast cancer anticipated to being enrolling in the fourth quarter. Filing
  3. Sep 10, 2026
    started Prelude's Phase 1 study of PRT12396, a JAK2V617F mutant selective inhibitor, is now enrolling MF and PV cohorts in parallel.MF & PV cohorts enrolling in parallel Filing

For subscribers

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