Outlook Therapeutics® to Report Financial Results for Third Quarter Fiscal Year 2024 on August 14, 2024 and Host Quarterly Conference Call and Webcast
August 07 2024 - 8:35AM
Outlook Therapeutics, Inc. (Nasdaq: OTLK), a biopharmaceutical
company that has achieved regulatory approval in the EU and UK for
the first authorized use of an ophthalmic formulation of
bevacizumab for the treatment of wet AMD, today announced that it
will report its financial results for third quarter fiscal year
2024 on Wednesday, August 14, 2024. Outlook Therapeutics management
will host its quarterly conference call and live audio webcast to
discuss the operational and financial results at 8:30 AM ET that
same day.
The call will be led by Russell Trenary,
President and Chief Executive Officer and Lawrence Kenyon, Chief
Financial Officer of Outlook Therapeutics. Interested participants
and investors may access the conference call by dialing (877)
407-8291 (domestic) or (201) 689-8345 (international) and
referencing the Outlook Therapeutics Conference Call. The live
webcast will be accessible on the Events page of the Investors
section of the Outlook Therapeutics website,
outlooktherapeutics.com, and will be archived for 90
days.
About Outlook Therapeutics,
Inc.
Outlook Therapeutics is a biopharmaceutical
company focused on the development and commercialization of
ONS-5010/LYTENAVA™ (bevacizumab-vikg; bevacizumab gamma), for the
treatment of retina diseases, including wet AMD. LYTENAVA™
(bevacizumab gamma) is the first ophthalmic formulation of
bevacizumab to receive European Commission and United Kingdom
Marketing Authorization for the treatment of wet AMD. Outlook
Therapeutics is working to initiate its commercial launch of
LYTENAVA™ (bevacizumab gamma) in the EU and the UK as a treatment
for wet AMD in the first calendar quarter of 2025. In the United
States, ONS-5010/LYTENAVA™ 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 application to the FDA in the United States. If
approved in the United States, ONS-5010/LYTENAVA™, would be the
first approved ophthalmic formulation of bevacizumab for use in
retinal indications, including wet AMD. For more information,
please visit www.outlooktherapeutics.com.
Investor
Inquiries: Jenene
ThomasChief Executive OfficerJTC Team, LLCT:
833.475.8247 OTLK@jtcir.com
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