Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SCD411 is a proposed biosimilar to aflibercept (marketed as Eylea), developed for the treatment of neovascular (wet) age-related macular degeneration. Like reference aflibercept, SCD411 is a recombinant fusion protein produced in Chinese hamster ovary cells using recombinant DNA technology. It acts by binding to vascular endothelial growth factor A (VEGF-A) and placental growth factor (PGF), thereby inhibiting their activity and preventing abnormal blood vessel growth in the eye. Clinical studies have demonstrated that SCD411 has equivalent efficacy, safety, pharmacokinetics, and immunogenicity compared with reference aflibercept[1][6][7]. The drug is administered via intravitreal injection.
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 SCD411.