Outlook Therapeutics® Participates in the 2nd Annual Chardan Virtual Ophthalmology Conference Series
2024年9月13日 - 10:05PM
Outlook Therapeutics, Inc. (Nasdaq: OTLK), a biopharmaceutical
company that achieved regulatory approval in the European Union and
the United Kingdom earlier 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
that the Company recently participated in the 2nd Annual Chardan
Virtual Ophthalmology Conference Series.
Chardan’s 2nd Annual Virtual Ophthalmology
Summit focused on age-related macular degeneration (AMD) and
diabetes-related ocular diseases and featured 8 companies pursuing
various differentiated approaches in treating serious eye
conditions, including Outlook Therapeutics. As part of the virtual
event, Russell Trenary, President and Chief Executive Officer and
Lawrence Kenyon, Chief Executive Officer of Outlook Therapeutics
participated in a fireside chat hosted by Daniil Gataulin, PhD,
Senior Research Analyst at Chardan.
A video webcast of the fireside chat is now
available here.
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 MHRA 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, expected in
the first half of calendar 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 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.
Investor
Inquiries:
Jenene Thomas Chief Executive Officer JTC Team, LLC T: 833.475.8247
OTLK@jtcir.com
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