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Werewolf Therapeutics receives FTD from U.S. FDA for WTX-124

Werewolf Therapeutics (HOWL) announced that the Company has received Fast Track Designation, FTD, for the use of WTX-124 for the potential treatment of patients with locally advanced or metastatic cutaneous melanoma after standard of care immunotherapy. WTX-124 is a conditionally activated interleukin 2 INDUKINE therapy. Fast Track Designation is intended to expedite the development of drugs to address a serious unmet medical need and provide opportunities for frequent FDA interactions.

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