Outlook Therapeutics® to Participate in the Cantor Fitzgerald Medical & Aesthetic Dermatology, Ophthalmology & Medtech Conference

Rhea-AI Summary

Outlook Therapeutics (Nasdaq: OTLK) announced that Russ Trenary, its President and CEO, will speak at a panel discussion on December 8, 2022, at 2:45 PM ET. The event, titled “Take A Look At What's In Store For Wet AMD & Related Diabetic Eye Diseases,” is part of the Cantor Fitzgerald Medical Conference. Alongside the discussion, Outlook Therapeutics will hold in-person meetings with investors. The company is focused on launching ONS-5010, the first FDA-approved ophthalmic formulation of bevacizumab for retinal diseases, with its BLA submission accepted by the FDA.

Russ Trenary, President and Chief Executive Officer of Outlook Therapeutics to participate in a live moderated panel discussion on Thursday, December 8th at 2:45 PM ET

ISELIN, N.J., Dec. 01, 2022 (GLOBE NEWSWIRE) -- Outlook Therapeutics, Inc. (Nasdaq: OTLK), a biopharmaceutical company working to develop and launch the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, today announced that Russ Trenary, President and Chief Executive Officer of Outlook Therapeutics, will participate in a panel discussion titled, “Take A Look At What's In Store For Wet AMD & Related Diabetic Eye Diseases,” at the Cantor Fitzgerald Medical & Aesthetic Dermatology, Ophthalmology & Medtech Conference on Thursday, December 8, 2022 at 2:45 PM ET.

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

The panel discussion is open to those who are registered to attend the event. Please contact your Cantor representative for more information.

About Outlook Therapeutics, Inc.
Outlook Therapeutics is a biopharmaceutical company working to develop and launch ONS-5010/ LYTENAVA™ (bevacizumab-vikg) as the first FDA-approved ophthalmic formulation of bevacizumab for use in retinal indications, including wet AMD, DME and BRVO. The FDA accepted Outlook Therapeutics’ BLA submission for ONS-5010 to treat wet AMD with a PDUFA goal date of August 29, 2023. The submission is supported by Outlook Therapeutics’ wet AMD clinical program, which consists of three clinical trials: NORSE ONE, NORSE TWO, and NORSE THREE. If ONS-5010 ophthalmic bevacizumab is approved, Outlook Therapeutics expects to commercialize it as the first and only FDA-approved ophthalmic formulation of bevacizumab for use in treating retinal diseases in the United States, United Kingdom, Europe, Japan, and other markets. For more information, please visit www.outlooktherapeutics.com.

CONTACTS:
Media Inquiries:
Anna Army
Account Supervisor
LaVoie Health Science
T: 617-351-0246
aarmy@lavoiehealthscience.com

Investor Inquiries:
Jenene Thomas
Chief Executive Officer
JTC Team, LLC
T: 833.475.8247 
OTLK@jtcir.com

FAQ

What is the date and time of the Outlook Therapeutics panel discussion?

The panel discussion featuring Russ Trenary is scheduled for December 8, 2022, at 2:45 PM ET.

What is the focus of the panel discussion involving Outlook Therapeutics?

The panel discussion will focus on wet AMD and related diabetic eye diseases.

What is Outlook Therapeutics' ticker symbol on Nasdaq?

The ticker symbol for Outlook Therapeutics is OTLK.

When is the PDUFA goal date for Outlook Therapeutics' ONS-5010 submission?

The PDUFA goal date for ONS-5010, submitted to treat wet AMD, is August 29, 2023.

What new product is Outlook Therapeutics developing?

Outlook Therapeutics is developing ONS-5010, the first FDA-approved ophthalmic formulation of bevacizumab for retinal indications.