Reata Pharmaceuticals, Inc. Loss Submission Form

Company: Reata Pharmaceuticals, Inc.

Ticker: (NASDAQ) RETA

Deadline

Passed

Lead Plaintiff Deadline: February 18, 2022

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Allegations

(1) the Food and Drug Administration had raised concerns regarding the validity of the clinical study designed to measure the efficacy and safety of bardoxolone for the treatment of chronic kidney disease caused by Alport syndrome; (2) as a result, there was a material risk that Reata’s New Drug Application would not be approved; and (3) as a result of the foregoing, defendants’ positive statements about the Company’s business, operations, and prospects were materially misleading and/or lacked a reasonable basis.