Durect corporation receives fda breakthrough therapy designation for larsucosterol in alcohol-associated hepatitis

Durect plans to confirm the efficacy and safety of larsucosterol in a registrational phase 3 clinical trial  cupertino, calif. , may 21, 2024 /prnewswire/ -- durect corporation (nasdaq: drrx), a late-stage biopharmaceutical company pioneering the development of epigenetic therapies to transform the treatment of serious and life-threatening conditions such as acute organ injury and cancer, today announced that the u.s. food and drug administration (fda) has granted breakthrough therapy designation (btd) to larsucosterol for the treatment of patients with severe alcohol-associated hepatitis (ah).
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