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Reata Pharmaceuticals Receives Complete Response Letter From The FDA for Bardoxolone for the Treatment of Patients with Chronic Kidney Disease Caused by Alport Syndrome

Reata Pharmaceuticals, Inc. (NASDAQ:RETA) ("Reata," the "Company," or "we"), today announced that the U.S. Food and Drug Administration ("FDA") has issued a Complete Response Letter ("CRL") regarding the New Drug Application ("NDA") for bardoxolone meth