July 24, 2026
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The FDA approved Lytenava for the treatment of neovascular age-related macular degeneration, according to a press release from Outlook Therapeutics.The approval of Lytenava is marks the first and only FDA-approved ophthalmic formulation of bevacizumab for the treatment of wet AMD in the United States.
July 24, 2026
1 min read
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Outlook Therapeutics (OTLK) announced that the Food and Drug Administration has approved Lytenava for the treatment of…

Approval follows 20 years of off-label use of compounded formulations of the VEGF inhibitor

The FDA approved LYTENAVA by Outlook Therapeutics, marking the first ophthalmic bevacizumab for wet AMD in the lucrative US…

Outlook Therapeutics resubmitted a biologics license application to the FDA for ONS-5010 for the treatment of neovascular…

Roche’s cancer treatment Avastin (bevacizumab) has long been employed as an off-label option for wet age-related macular…

Outlook Therapeutics shares rose after the FDA accepted its resubmitted LYTENAVA BLA and set a July 2026 target action date.

Outlook Therapeutics Targets Multibillion Dollar Ophthalmology Market With New Drug After FDA Rejection -