FDA Approves IND Application for TUL108 Injection from The United Laboratories

Reuters01-28
FDA Approves IND Application for TUL108 Injection from The United Laboratories

The United Laboratories International Holdings Limited announced that its wholly-owned subsidiary, Zhuhai United Laboratories Co., Ltd., has received approval from the U.S. Food and Drug Administration (FDA) for its investigational new drug $(IND)$ application for TUL108 for injection. TUL108 is a novel, broad-spectrum β-lactamase inhibitor developed by the company, intended for the treatment of infections caused by Gram-negative or Gram-positive bacteria, including complicated urinary tract infections, complicated intra-abdominal infections, pulmonary infections, and bloodstream infections. The IND approval allows the company to proceed with clinical development of TUL108 in the United States.

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