FDA approves Eylea 12-week dosing for wet AMD

The FDA has approved a supplemental biologics license application for a 12-week dosing schedule of Eylea injection in wet age-related macular degeneration patients, Regeneron announced in a press release.
The FDA previously issued a complete response letter to Regeneron regarding the sBLA, which is based on data from the phase 3 VIEW 1 and 2 trials, in which wet AMD patients received Eylea (aflibercept) injections at least every 12 weeks, with additional doses as needed.
“We are pleased that the FDA has approved an updated label for Eylea,” George D. (Read more...)

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