Outlook Therapeutics Announces FDA Acceptance of Resubmitted Biologics License Application for ONS-5010/LYTENAVA™ (bevacizumab-vikg) as a Treatment for Wet AMD
ISELIN, N.J., June 16, 2026 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (https://www.globenewswire.com/Tracker?data=9945MzUs41eabzIabJnYh5CBADTPYamlUOYj5GE0LL56UHq16pd9QqXXA-g7HF4E7rnufYDyBStlrI8k5f9LM5WUPbwpZvXNjrrARqaVBcMTWwMeNAM27761a-HU9MKl) (Nasdaq: OTLK), a biopharmaceutical company focused on enhancing the standard of care for bevacizumab for the treatment of retina diseases, today announced the U.S. Food and Drug Administration (FDA) has acknowledged receipt of the resubmission of the
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