CSPC wins FDA approval to start U.S. trials of SYH2059 inhalation powder for pulmonary fibrosis

Reuters03-06 19:41

CSPC Pharmaceutical Group Ltd said the U.S. FDA has approved clinical trials for its SYH2059 powder for inhalation. SYH2059 is a highly selective PDE4B inhibitor being developed for pulmonary fibrosis, including idiopathic pulmonary fibrosis and progressive pulmonary fibrosis.

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-20260306-12044550), on March 06, 2026, and is solely responsible for the information contained therein.

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