Outlook Therapeutics® to Present at the Guggenheim Healthcare Innovation Conference

OTLK 11.06.2024

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  • 01.22.2025 - Outlook Therapeutics® to Present at LIVE! with Webull Corporate Connect: Healthcare Investment Webinar
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Live fireside chat with CEO, Russ Trenary, on November 12th at 2:30 PM ET

ISELIN, N.J.,Nov. 06, 2024(GLOBE NEWSWIRE) --Outlook Therapeutics, Inc.(Nasdaq: OTLK), a biopharmaceutical company that achieved regulatory approval in theEuropean Unionand theUnited Kingdomearlier this year for the first authorized use of an ophthalmic formulation of bevacizumab for the treatment of wet age-related macular degeneration (wet AMD), today announced thatRussell Trenary, President and CEOofOutlook Therapeuticswill participate in a fireside chat onTuesday, November 12, 2024at2:30 PM ETat theGuggenheim Healthcare Innovation Conferencebeing held inBoston, MA.

In addition to the fireside chat, management will be available to participate in one-on-one in-person meetings with qualified members of the investor community who are registered to attend the conference.

Alive webcastof the fireside chat will be accessible on theEventspage in theInvestorssection of the Company’s website (outlooktherapeutics.com). The webcast replay will be archived for 90 days following the event.

AboutOutlook Therapeutics, Inc.

Outlook Therapeuticsis a biopharmaceutical company focused on the development and commercialization of ONS-5010/LYTENAVATM (bevacizumab-vikg; bevacizumab gamma), for the treatment of retina diseases, including wet AMD. LYTENAVATM (bevacizumab gamma) is the first ophthalmic formulation of bevacizumab to receiveEuropean Commissionand MHRA Marketing Authorization for the treatment of wet AMD.Outlook Therapeuticsis working to initiate its commercial launch of LYTENAVATM (bevacizumab gamma) in the EU and theUKas a treatment for wet AMD, expected in the first half of calendar 2025. Inthe United States, ONS-5010/LYTENAVATM is investigational, is being evaluated in an ongoing non-inferiority study for the treatment of wet AMD, and if successful, the data may be sufficient for Outlook to resubmit a BLA to the FDA inthe United States. If approved inthe United States, ONS-5010/LYTENAVATM, would be the first approved ophthalmic formulation of bevacizumab for use in retinal indications, including wet AMD.

Investor Inquiries:Jenene ThomasChief Executive OfficerJTC Team, LLCT: 908.824.0775OTLK@jtcir.com

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Source: Outlook Therapeutics, Inc.

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