MONMOUTH JUNCTION, N.J. , July 17, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK), a late clinical-stage biopharmaceutical company working to develop the first FDA-approved ophthalmic formulation of bevacizumab-vikg for use in retinal indications, today announced the successful

Pivotal NORSE 2 safety and efficacy data expected to be reported in the third calendar quarter of 2021   ONS-5010 / LYTENAVA ™   (bevacizumab-vikg)   has the potential to be the first FDA-approved ophthalmic formulation of bevacizumab for use in multiple retinal indications MONMOUTH JUNCTION, N.J.

MONMOUTH JUNCTION, N.J. , June 25, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK) (“the Company”), a late clinical-stage biopharmaceutical company working to develop the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, today announced that

MONMOUTH JUNCTION, N.J. , June 23, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK) (“the Company”), a late clinical-stage biopharmaceutical company working to develop the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, today announced that

Lead product candidate ONS-5010 / LYTENAVA TM   (bevacizumab-vikg)   has potential to be first FDA-approved ophthalmic formulation of bevacizumab for use in multiple retinal indications   Topline results from NORSE 1, the Company’s first registration clinical trial evaluating ONS-5010 and providing

MONMOUTH JUNCTION, N.J. , June 11, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK) (the Company), a late clinical-stage biopharmaceutical company working to develop the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, announced today that

Live moderated video webcast discussion with President, CEO and CFO Lawrence Kenyon, on Wednesday, June 17th at 2:00 PM ET, immediately followed by an interactive Q&A session MONMOUTH JUNCTION, N.J. , June 09, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc.

MONMOUTH JUNCTION, N.J. , June 03, 2020 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK) (the Company), a late clinical-stage biopharmaceutical company working to develop the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, today announced the

Strategic investment at a premium enhances Company’s ongoing development activities of ONS-5010 / LYTENAVA™ (bevacizumab-vikg), an investigational ophthalmic formulation of bevacizumab to treat wet AMD, toward FDA approval   Syntone and Outlook to form joint venture to develop and commercialize

Company remains on track to report topline data results from NORSE 1, its first registration clinical trial evaluating ONS-5010, an investigational ophthalmic formulation of bevacizumab to treat wet AMD, in August 2020   Enrollment in NORSE 2 registration clinical trial remains ongoing and is