Ocular Therapeutix™ to Present Data at the American Academy of Optometry Annual Meeting 2021
Ocular Therapeutix (NASDAQ:OCUL) announced key scientific presentations at the American Academy of Optometry Annual Meeting 2021 in Boston, MA, from November 3-6. The company highlighted DEXTENZA® for treating ocular inflammation, pain, and itching associated with allergic conjunctivitis. Presentations include analyses of a hydrogel-based dexamethasone insert and comparisons of treatment methods for conditions like keratoconus and dry eye. All presentations will be available on the company’s website starting November 5.
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“The AAOPT is the largest meeting in optometry and works to maintain and enhance excellence in optometric practice, by both promoting research and the dissemination of knowledge,” said
Presentations / Posters
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Title: Pooled Analysis of a Hydrogel-based Intracanalicular Dexamethasone Insert for the Treatment of Allergic Conjunctivitis
Presenter:Walter Whitley , OD
Date / Time:Thursday, November 4 th, 4:30 –6:30pm ET
Location: Podium Presentation, Room 253ABC -
Title: Effects of Punctal Occlusion on Ocular Itching and Conjunctival Redness Associated with Allergic Conjunctivitis
Presenter: Nysha Blender, OD
Date / Time:Friday, November 5 th,10:00am –12:00pm ET
Location: Poster Board #27, Exhibit Hall B1
Investigator-initiated Trial Presentations
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Title: Comparison of Intracanalicular Dexamethasone Insert to Loteprednol Etabonate Ophthalmic gel
0.38% in Patients with Keratoconus, Allergies and Dry Eye
Presenter:Jennifer Harthan , OD
Date / Time:Thursday, November 4 th, 4:30 –6:30pm ET
Location: Poster Board #99, Exhibit Hall B1 -
Title: Comparison of Preoperative vs Postoperative Dexamethasone Intracanalicular Insert Placement in Controlling Pain & Inflammation following CE/PCIOL.
Presenter:Lindsey Harris , OD
Date / Time:Friday, November 5 th,10:00am –12:00pm ET
Location: Poster Board #29, Exhibit Hall B1
All presentations will be available as of
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 commercial launch of, and effectiveness of reimbursement codes for, DEXTENZA; the conduct of post-approval studies of and compliance with related labeling requirements for DEXTENZA and ReSure Sealant; the development and regulatory status of the Company’s product candidates, such as the Company’s development of and prospects for approvability of OTX-CSI for the chronic treatment of dry eye disease, OTX-DED for the short-term treatment of the signs and symptoms of dry eye disease, OTX-TIC for the treatment of primary open-angle glaucoma or ocular hypertension, and OTX-TKI for the treatment of retinal diseases including wet AMD; the ongoing development of the Company’s extended-delivery hydrogel depot technology; the size of potential markets for our product candidates; the potential utility of any of 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; potential market sizes for indications targeted by the Company’s product candidates, if approved; the expected impact of the COVID-19 pandemic on the Company and its operations; the sufficiency of the Company’s cash resources 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, availability of data from clinical trials and expectations for regulatory submissions and approvals, the interpretation of data from the Company’s clinical trials, including interim data such as the data referred to above which may not be indicative of the full data from a trial, 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 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 and relevant regulatory authorities’ operations, any additional financing needs 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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Chief Financial Officer
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or
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Managing Director
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Media
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