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Relay Therapeutics announces U.S. FDA granted BTD to zovegalisib

Relay Therapeutics (RLAY) announced that the U.S. Food and Drug Administration, FDA, has granted Breakthrough Therapy designation, BTD, to zovegalisib in combination with fulvestrant for the treatment of adults with PIK3CA mutant, hormone receptor positive, human epidermal growth factor receptor 2-negative locally advanced or metastatic breast cancer following recurrence or progression on or after treatment with a CDK4/6 inhibitor.

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