10/08/2025
Werewolf Therapeutics is excited to announce the U.S. FDA has granted Fast Track Designation to WTX-124 for the potential treatment of patients with locally advanced or metastatic cutaneous after standard of care immunotherapy.
This milestone reflects our unwavering commitment to patients who face limited treatment options. We look forward to working closely with the FDA to advance this therapy and deliver meaningful progress.
Read more: https://investors.werewolftx.com/news-releases/news-release-details/werewolf-therapeutics-receives-fast-track-designation-us-fda-wtx