Qyuns Therapeutics’ Crusekitug NDA for adult ankylosing spondylitis accepted by China’s NMPA

Reuters03-09

Qyuns <a href="https://laohu8.com/S/LENZ">Therapeutics</a>’ Crusekitug NDA for adult ankylosing spondylitis accepted by China’s NMPA

Qyuns Therapeutics said China’s National Medical Products Administration accepted its new drug application for Crusekitug (QX002N) to treat active ankylosing spondylitis in adults. The application is supported by a Phase III trial (CTR20232574) that reported 52-week efficacy and safety results.

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. Qyuns Therapeutics Co. 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-20260309-12046137), on March 09, 2026, and is solely responsible for the information contained therein.

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