Chinese biopharmaceutical company Kexing Biopharm Co Ltd (SHA:688136) announced on Thursday that the first subject has been enrolled and dosed in the Phase I clinical trial in China for GB10 Injection, an innovative ophthalmic drug independently developed by its subsidiary Shenzhen Kexing Pharmaceutical Co Ltd.
Designed to treat neovascular age-related macular degeneration (nAMD), GB10 is a high-concentration, ophthalmic protein drug formulation that features a bispecific antibody targeting both VEGF and Ang-2. The company says that with a high concentration of 140 mg/mL, GB10 Injection allows for a smaller injection volume or higher dosage, thereby extending the dosing interval. It is expected to achieve a 'once per four months' dosing schedule, significantly improving patient compliance.
Preclinical data indicate international competitiveness of GB10 Injection in terms of both biological activity and in vivo efficacy. In a laser-induced choroidal neovascularisation (CNV) monkey model, it demonstrated effective inhibition of pathological ocular neovascularisation in the fundus.
nAMD remains a leading cause of blindness globally among individuals aged over 50.
Persist AI partners with Microsize and Micromacinazione to launch drug formulation platform
RedHill Biopharma advancing opaganib options for Ebola outbreak
Sun Pharma receives American Skin Association 2026 Corporate Leadership Award
Evogene completes Phase 1 study of BMC128 in combination with Nivolumab
FDA accepts Genentech's giredestrant application for early-stage breast cancer
Ansun Biopharma reports positive recommendation from independent DMC for DAS181