Ocular Therapeutix™ To Present Data at the American Academy of Ophthalmology (AAO) 2022 Annual Meeting
Ocular Therapeutix, Inc. (NASDAQ:OCUL) announced its significant presence at the American Academy of Ophthalmology (AAO) 2022 Annual Meeting, held from September 30 to October 3, 2022, in Chicago, IL. The company will present key findings, including 28-week data on its Phase 1 trial of OTX-TKI for Wet AMD. Presentations include podium talks and ePosters on various ophthalmic conditions, emphasizing their product candidates like DEXTENZA and OTX-TKI. Ocular Therapeutix is focused on innovative therapies for eye diseases using hydrogel technology.
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“We have a big presence at AAO this year with many presentations discussing product candidates across multiple ophthalmic indications, with an emphasis on retina,” said
Eyecelerator @ AAO 2022 Retina Showcase Presentation:
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Session Title: Presenting Company Showcase: Retina, Therapeutics, and Technology + Devices
Presentation Date/Times :Thursday, September 29, 2022 , 2:00 –2:05 PM CDT
Location:McCormick Place Convention Center
Presentation type: Podium Presentation
Presenter:Peter K. Kaiser , MD
Retina Subspecialty Day Presentation:
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Title: Interim Safety and Efficacy Data from a Phase 1 Clinical Trial of Sustained-release Axitinib Hydrogel Implant (OTX-TKI) in Wet AMD Subjects
Session Title: Late Breaking Developments, Part I (RET09)
Presentation Date/Times :Friday, September 30, 2022 ,3:29-3:34 PM CDT
Location: Arie Crown
Presentation type: Podium Presentation
Presenter:Dilsher S. Dhoot , MD
Poster Theater Presentation:
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Title: Real-World Safety Analysis of an Intracanalicular Dexamethasone Insert Using the Academy's IRIS® Registry
Session Title: Cataract (PT01)
Presentation Date/Times :Saturday, October 1, 2022 ,9:40-9:50 AM CDT
Location:Hall A Poster Theater and Lounge
Presentation type:Poster Theatre
Presenter:Robert T. Chang , MD
ePosters:
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Title: Real-World Patient Demographics and Clinical Characteristics of an Intracanalicular Dexamethasone Insert Using the Academy’s IRIS® Registry
Session Title: Cataract
Viewing Date/Times :Tuesday, September 27, 2022 starting at9:00 AM CDT
Presentation type: ePoster (PO021)
Presenter:Michael Mbagwu , MD
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Title: Interim 28-weeks Data from a Phase 1 US Study of Sustained-release Axitinib Hydrogel Implant (OTX-TKI) in Previously Treated Wet AMD Subjects
Session Title: Retina, Vitreous
Viewing Date/Times :Friday, September 30, 2022 starting at5:00 PM CDT
Presentation type: ePoster (PO359)
Presenter:Arshad M. Khanani , MD
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Title:
Australia -based Phase 1 Trial of a Novel, Hydrogel-based, Intravitreal Axitinib Implant for the Treatment of Neovascular Age-related Macular Degeneration
Session Title: Retina, Vitreous
Viewing Date/Times :Friday, September 30, 2022 starting at5:00 PM CDT
Presentation type: ePoster (PO360)
Presenter:Andrew A. Moshfeghi , MD
About
Forward Looking Statements
Any statements in this press release about future expectations, plans, and prospects for the Company, including the commercialization of DEXTENZA®, ReSure® Sealant, or any of the Company’s product candidates; the development and regulatory status of the Company’s product candidates, such as the Company’s development of and prospects for approvability of OTX-TIC for the treatment of primary open-angle glaucoma or ocular hypertension, OTX-TKI for the treatment of retinal diseases including wet AMD, OTX-DED for the short-term treatment of the signs and symptoms of dry eye disease, and OTX-CSI for the chronic treatment of dry eye disease; the Company’s plans to advance the development of its product candidates or preclinical programs; the ongoing development of the Company’s extended-delivery hydrogel depot technology; the potential utility of any of the Company’s product candidates; the size of potential markets for the Company’s product candidates; the potential benefits and future operations of Company collaborations, including any potential future costs or payments thereunder; projected net product revenue, in-market sales and other financial and operational metrics of DEXTENZA and ReSure Sealant; the sufficiency of the Company’s cash resources; the Company’s anticipated participation in future presentations and medical conferences; and other statements containing the words "anticipate," "believe," "estimate," "expect," "intend", "goal," "may", "might," "plan," "predict," "project," "target," "potential," "will," "would," "could," "should," "continue," and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors. Such forward-looking statements involve substantial risks and uncertainties that could cause the Company’s preclinical and clinical development programs, future results, performance or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the timing and costs involved in commercializing DEXTENZA, ReSure Sealant or any product candidate that receives regulatory approval, including the conduct of post-approval studies, the ability to successfully develop and commercialize products for the ophthalmology office setting, the ability to retain regulatory approval of DEXTENZA, ReSure Sealant or any product candidate that receives regulatory approval, the ability to maintain and the sufficiency of product, procedure and any other reimbursement codes for DEXTENZA, the initiation, timing, conduct and outcomes of clinical trials, whether clinical trial data such as the data reported in this release will be indicative of the results of subsequent clinical trials, availability of data from clinical trials and expectations for regulatory submissions and approvals, the Company’s ability to enter into and perform its obligations under collaborations and the performance of its collaborators under such collaborations, the Company’s scientific approach and general development progress, the availability or commercial potential of the Company’s product candidates, the Company’s ability to meet supply demands, the Company’s ability to generate its projected net product revenue and in-market sales on the timeline expected, if at all, the sufficiency of cash resources, the Company’s existing indebtedness, the ability of the Company’s creditors to accelerate the maturity of such indebtedness upon the occurrence of certain events of default, the severity and duration of the COVID-19 pandemic including its effect on the Company’s revenues and relevant regulatory authorities’ operations, any additional financing needs, the Company’s ability to recruit and retain key personnel, and other factors discussed in the “Risk Factors” section contained in the Company’s quarterly and annual reports on file with the
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