Kexing Biopharm GB10 Phase I Trial
Analysis based on 7 articles · First reported Jun 04, 2026 · Last updated Jun 04, 2026
The initiation of Phase I clinical trials for GB10 Injection by Shenzhen Kexing Pharmaceutical Co., Ltd., a subsidiary of Kexing Biopharm, is a positive development for the pharmaceutical and biotechnology sectors. This could lead to increased investor confidence in Kexing Biopharm's R&D capabilities and future market potential, especially given the high demand for ophthalmic treatments.
Shenzhen Kexing Pharmaceutical Co., Ltd., a wholly-owned subsidiary of Kexing Biopharm, has enrolled and dosed the first subject in a Phase I clinical trial in China for its innovative ophthalmic drug, GB10 Injection. This drug is designed to treat neovascular age-related macular degeneration (nAMD), a leading cause of blindness. GB10 Injection is a high-concentration, bispecific antibody targeting both VEGF and Ang-2, with preclinical data showing international competitiveness. Its expected 'once per four months' dosing schedule aims to significantly improve patient compliance, addressing a critical clinical pain point. This milestone accelerates Kexing Biopharm's innovative drug R&D pipeline and supports its strategy to expand its global footprint through continuous innovation, including introducing other ophthalmic products like Aflibercept biosimilar and Olopatadine Hydrochloride eye drops.
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