Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GP20101 is a biosimilar candidate of ranibizumab (Lucentis), developed by the Russian pharmaceutical company Geropharm. It is a recombinant humanized monoclonal antibody fragment (Fab) produced in *Escherichia coli* that binds to and inhibits vascular endothelial growth factor A (VEGF-A). By neutralizing VEGF-A, GP20101 prevents the activation of VEGFR1 and VEGFR2 receptors on the surface of endothelial cells, thereby inhibiting the abnormal proliferation of blood vessels (angiogenesis) and reducing vascular permeability in the retina. The drug is primarily being developed for the treatment of neovascular (wet) age-related macular degeneration (nAMD) and other retinal vascular disorders. It is currently in Phase 3 clinical development to demonstrate therapeutic equivalence, safety, and immunogenicity compared to the reference product.
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 GP20101.