FDA advisors cheer on Lucentis for DMO
This article was originally published in Scrip
Executive Summary
The USFDA ophthalmic drugs advisory committee did more than recommend that the agency approve the pending biologics license application (BLA) from Roche's Genentech arm to add to the label for Lucentis (ranibizumab) a new indication for the treatment of diabetic macular oedema (DMO). The outside experts aggressively cheered the drug.