China Medical System’s MG-K10 Seasonal Allergic Rhinitis NDA Accepted by NMPA

SGX Filings
Apr 23

China Medical System Holdings Limited announced that on Apr, 23 2026 China’s National Medical Products Administration accepted the new drug application for MG-K10 (Comekibart Injection) to treat adult patients with moderate-to-severe seasonal allergic rhinitis whose symptoms remain inadequately controlled after intranasal corticosteroid therapy.

MG-K10 is a long-acting anti-IL-4Rα humanized monoclonal antibody that blocks IL-4 and IL-13 signaling and is administered once every four weeks. The drug met its primary endpoint in a multicenter Phase III trial, showing superior efficacy versus placebo with a favorable safety profile.

The regulatory milestone broadens the company’s CMS Vision unit from ophthalmology into otolaryngology and advances its pipeline in type 2 inflammatory diseases.

Under a collaboration signed on Jan, 24 2025 with Hunan Mabgeek Biotech Co., Ltd., China Medical System holds co-development rights (excluding atopic dermatitis) and exclusive commercialization rights for MG-K10 in Mainland China, Hong Kong, Macao, Taiwan and Singapore.

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