Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
QBR202 is a long-acting biologic agent designed to inhibit vascular endothelial growth factor (VEGF), currently under development by Beijing Xunji Biotechnology for the treatment of retinal vascular disorders. The drug is primarily indicated for neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME). By targeting and neutralizing VEGF-A, QBR202 aims to suppress the pathological angiogenesis and vascular permeability that drive vision loss in these conditions. It is administered via intravitreal injection and is currently being evaluated in Phase I clinical trials in China to assess its safety, tolerability, and preliminary efficacy.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on QBR202.