CSPC Pharmaceutical Group Wins US FDA Approval for SYH2072 Clinical Trials

Reuters01-13

CSPC Pharmaceutical Group Wins US FDA Approval for SYH2072 Clinical Trials

CSPC Pharmaceutical Group Ltd. has announced that its potent aldosterone synthase inhibitor, SYH2072 tablets, has obtained approval from the U.S. Food and Drug Administration to conduct clinical trials in the United States. The product also received clinical trial approval from the National Medical Products Administration of China in December 2025. SYH2072 is a highly selective aldosterone synthase inhibitor intended for the treatment of uncontrolled hypertension and resistant hypertension.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. CSPC Pharmaceutical Group Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260113-11989177), on January 13, 2026, and is solely responsible for the information contained therein.

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