Prelude Therapeutics Receives FDA Clearance for PRT12396 Phase 1 Study
ByAinvest
Tuesday, Feb 3, 2026 9:15 am ET1min read
PRLD--
Prelude Therapeutics has received FDA clearance for its Investigational New Drug Application (IND) for PRT12396, a mutant-selective JAK2V617F inhibitor. The Phase 1 study in patients with polycythemia vera and myelofibrosis is expected to initiate by Q2 2026. This marks a significant milestone in the development of PRT12396 for the treatment of certain myeloproliferative neoplasms (MPNs).
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