Akeso sNDA for Gumokimab in Ankylosing Spondylitis Accepted for NMPA Review

Reuters01-19

Akeso sNDA for Gumokimab in Ankylosing Spondylitis Accepted for NMPA Review

Akeso Inc. announced that the National Medical Products Administration (NMPA) in China has accepted the supplemental New Drug Application (sNDA) for gumokimab (AK111), a humanized anti-IL-17A monoclonal antibody, for the treatment of active ankylosing spondylitis. This marks the second indication for gumokimab to receive NDA review, following its earlier acceptance for moderate-to-severe psoriasis. The NDA acceptance is supported by positive results from a pivotal Phase III clinical trial, which demonstrated significant improvements in symptoms and quality of life for patients with active ankylosing spondylitis.

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. Akeso Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN65925) on January 19, 2026, and is solely responsible for the information contained therein.

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