FDA Fast Track Designation for PHST001 for the Treatment of Ovarian Cancer
“Receiving Fast Track designation from the FDA reinforces the promise of CD24 as a next-generation immuno-oncology target and highlights the potential of PHST001 to address a critical unmet need in the treatment of ovarian cancer,” said Raphaël Rousseau, M.D., Ph.D., Chief Medical Officer, Pheast Therapeutics. “We are committed to advancing PHST001 through the clinic and accelerating its development for cancer patients in urgent need of more effective treatments.”
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