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Outlook Therapeutics® Announces Commercial Launch of LYTENAVA™ (bevacizumab gamma) in Germany and the UK for the Treatment of Wet AMD

LYTENAVA™ is the first and only approved ophthalmic formulation of bevacizumab for the treatment of wet AMD in the European Union (EU) and United Kingdom (UK)2.8 million injections of repackaged off-label bevacizumab in Europe each year1 ISELIN, N.J., June 02, 2025 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK), a biopharmaceutical company focused on enhancing the standard of care for bevacizumab for the treatment of retina diseases, today announced that LYTENAVA™ (bevacizumab gam

articleOutlook Therapeutics, Inc.June 2, 20256/company/outlook-therapeutics-inc/news/outlook-therapeutics-announces-commercial-launch-110000217
Outlook Therapeutics® Announces Commercial Launch of LYTENAVA™ (bevacizumab gamma) in Germany and the UK for the Treatment of Wet AMD

About this update from Outlook Therapeutics, Inc.

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More updates from Outlook Therapeutics, Inc.

European Unionwet AMDbevacizumabUnited KingdomTherapeuticsOutlook teamEuropean CommissionVEGFgamma