The FDA has approved Genentech's prefilled ranibizumab syringe for injecting the eyes of people with wet age-related macular degeneration (wet AMD)
The US Food and Drug Administration (FDA) has approved a pre-filled syringe to administer ranibizumab (Lucentis PFS/Genentech-Roche).
The device will be available early next year.
Like the Lucentis 0.5mg vial, the syringe is approved to treat people with wet age-related macular degeneration (AMD) and macular edema after retinal vein occlusion (RVO).
Having a prefilled syringe should make it easier and safer for physicians to administer the eye injection, the company said in a news release.
An estimated 1.1 million people in the US have wet AMD. The drug was approved to treat the condition in 2006.
It is a vascular endothelial growth factor inhibitor designed to bind to and inhibit the protein that plays a role in angiogenesis and hyperpermeability of blood vessels.