Skip to Main Content

Acadia Pharmaceuticals said Monday that U.S. regulators had rejected its application seeking to expand the use of its anti-psychosis drug Nuplazid to a broader group of patients.

The decision by the Food and Drug Administration was widely expected following a March 8 letter sent by the agency to Acadia, citing undefined “deficiencies” in the Nuplazid application.

Unlock this article by subscribing to STAT+ and enjoy your first 30 days free!