Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ASKG712 is a novel bispecific biologic molecule specifically designed for ocular use in retinal diseases. It is composed of a vascular endothelial growth factor (VEGF)-inhibiting humanized monoclonal antibody fused with an angiopoietin-2 (Ang-2) antagonist peptide, forming a recombinant fusion protein. This dual-targeting approach enables simultaneous inhibition of VEGF and Ang-2 pathways, both of which are implicated in pathological neovascularization and vascular instability seen in conditions such as neovascular (wet) age-related macular degeneration (nAMD) and diabetic macular edema. Preclinical studies have demonstrated robust efficacy, strong binding affinity to VEGF and Ang-2, favorable ocular pharmacokinetics, and an anticipated safety profile supporting further clinical development[1][5][6][8][9]. The drug aims to improve clinical outcomes by reducing the frequency of intravitreal injections compared to current anti-VEGF monotherapies.
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 ASKG712.