Outlook Therapeutics to Present at the Retina Subspecialty Day, American Academy of Ophthalmology 2021 Annual Conference
November 04 2021 - 8:05AM
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 Firas M. Rahhal, MD,
Retina-Vitreous Associates Medical Group, Assoc. Clinical Professor
of Ophthalmology, UCLA School of Medicine, will present safety and
efficacy data from Outlook Therapeutics’ Phase 3 pivotal NORSE TWO
trial for ONS-5010 / LYTENAVA™ (bevacizumab-vikg), an
investigational ophthalmic formulation of bevacizumab for use in
retinal indications. Dr. Rahhal will present the data in an oral
presentation at the Retina Subspecialty Day of the American Academy
of Ophthalmology (AAO) 2021 Annual Conference being held in New
Orleans, Louisiana.
Details for the presentation are as follows:
Safety and Efficacy Results of ONS-5010,
an Ophthalmic Bevacizumab, Phase 3 Pivotal Study of Monthly
Intravitreal ONS-5010 in Subjects with Wet AMD (NORSE
TWO)Presenter: Firas M. Rahhal, MDSession: Section X: Late
Breaking Developments, Part IIDate and time: Saturday, November 13,
2021, at 9:17 AM EDT
For more information and to register for this
event, please visit AAO 2021.
About American Academy of
Ophthalmology
Launched in 1979, the American Academy of
Ophthalmology is the world’s largest association of eye physicians
and surgeons. A global community of 32,000 medical doctors, the AAO
serves to protect sight and empower lives by setting the standards
for ophthalmic education and advocating for patients and the
public. We innovate to advance our profession and to ensure the
delivery of the highest-quality eye care.
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. 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. Outlook Therapeutics expects to
submit ONS-5010 ophthalmic bevacizumab to the U.S. FDA as a BLA
under the PHSA 351(a) regulatory pathway. For more information,
please visit www.outlooktherapeutics.com.
CONTACTS:Media
Inquiries:Harriet UllmanVice PresidentLaVoie Health
ScienceT: 617-669-3082hullman@lavoiehealthscience.com
Investor
Inquiries: Jenene
ThomasChief Executive OfficerJTC Team, LLCT:
833.475.8247 OTLK@jtcir.com
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