FDA Accepts Resubmitted BLA For ONS-5010/LYTENAVA For Wet AMD With PDUFA Date Set For July 29, 2026 – Outlook Therapeutics
Outlook Therapeutics announced the FDA has acknowledged receipt of the resubmission of the Biologics License Application (BLA) for ONS-5010/LYTENAVA for the treatment of neovascular age-related macular degeneration (nAMD),… read more.




