Roche Pharma India has entered the field of ophthalmology with the introduction of Vabysmo (faricimab) for the treatment of neovascular or ‘wet’ age-related macular degeneration (nAMD) and diabetic macular edema (DME), prevalent causes of global vision loss. Vabysmo stands out as the inaugural dual-pathway-inhibitor, uniquely addressing two critical disease pathways associated with various sight-threatening retinal conditions. By neutralizing both angiopoietin-2 (Ang-2) and vascular endothelial growth factor-A (VEGF-A), pivotal proteins in retinal condition development, Vabysmo stabilizes blood vessels in the eye and combats vision loss.
Distinguished as the world’s premier bispecific monoclonal antibody (mAb), Vabysmo represents a singular molecule adept at targeting and inhibiting the effects of two crucial factors, offering the combined advantages of two medications in one. In contrast to current treatments exclusively targeting VEGF, Vabysmo introduces a groundbreaking approach by concurrently blocking pathways involving both Ang-2 and VEGF-A. This innovation marks the first new mechanism of action (MoA) in over 15 years for nAMD and nearly a decade for DME, promising to enhance vision outcomes by fortifying blood vessels in the retina.
Having gained approval from the USFDA in January 2022, Vabysmo is now accessible in over 90 countries, with over 2 million doses administered to date. Positioned as a potential game-changer, Vabysmo has the capacity to revolutionize the existing Standard of Care (SoC) by mitigating the burdens associated with current treatment options, such as frequent eye injections and physician visits, which often result in under-treatment and suboptimal vision outcomes.