Outlook therapeutics® receives european commission marketing authorization for lytenava™ (bevacizumab gamma) for the treatment of wet amd

Iselin, n.j., may 28, 2024 (globe newswire) -- outlook therapeutics, inc. (nasdaq: otlk), a biopharmaceutical company focused on the commercialization and development of ons-5010/lytenava™ (bevacizumab-vikg; bevacizumab gamma), for the treatment of retina diseases, today announced that the european commission has granted marketing authorization for lytenava™ (bevacizumab gamma), an ophthalmic formulation of bevacizumab for the treatment of wet amd in the eu. lytenava™ (bevacizumab gamma) is the first and only authorized ophthalmic formulation of bevacizumab for use in treating wet amd in the eu.
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