The US Food and Drug Administration's approval of Susvimo, a new port delivery system (PDS) for administration of a customized formulation of Roche Holding AG's Lucentis (ranibizumab), will provide the company with a continued commercial opportunity in neovascular age-related macular degeneration (nAMD or wet AMD) as Lucentis biosimilars approach the market.
Roche’s Genentech, Inc. subsidiary announced FDA approval of Susvimo (ranibizumab injection), a refillable eye implant for use with a...







