Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
KH631 is an investigational gene therapy for neovascular (wet) age-related macular degeneration (nAMD). It uses a recombinant adeno-associated virus 8 (rAAV8) vector to deliver a transgene encoding a human VEGF receptor fusion protein. This fusion protein consists of domain 2 of VEGFR1, domains 3 and 4 of VEGFR2, and the Fc domain of human IgG1. The expressed protein binds and inhibits vascular endothelial growth factor A (VEGF-A), VEGF-B, and placental growth factor (PlGF), thereby blocking angiogenesis in the retina. KH631 is administered as a single subretinal injection with the goal of providing long-term suppression of pathological neovascularization, potentially reducing or eliminating the need for frequent anti-VEGF injections. The therapy is being developed by Chengdu Kanghong Pharmaceutical for wet AMD and has entered phase I/II clinical trials in China and the United States[1][2][3][4][5][7].
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 KH631.