Ocular Therapeutix™ to Present Clinical Data at the 2022 American Society of Cataract and Refractive Surgery (ASCRS) Annual Meeting
Ocular Therapeutix (NASDAQ:OCUL) announced a strong presence at the 2022 American Society of Cataract and Refractive Surgery (ASCRS) Annual Meeting. The company showcased updates on DEXTENZA, an FDA-approved treatment for ocular inflammation and allergic conjunctivitis, along with the OTX-DED for dry eye disease. Multiple presentations highlighted the efficacy of these therapies, underscoring the potential of Ocular Therapeutix's hydrogel technology to address unmet needs in ophthalmic care. The meeting is set for April 22-26, 2022, in Washington, D.C.
- Significant presentations at the ASCRS Annual Meeting indicate strong market interest in DEXTENZA and OTX-DED.
- DETXENZA's FDA approval for treating ocular inflammation and pain enhances its marketability.
- Multiple studies showing the effectiveness and real-world application of DEXTENZA and OTX-DED.
- Proprietary hydrogel technology demonstrated potential to meet various ophthalmic treatment needs.
- None.
“We are excited to have such a large presence at this year’s ASCRS which we believe highlights the interest in DEXTENZA® as well as our other ocular surface programs,” commented
Ocular Therapeutix Presentations at ASCRS:
DEXTENZA® (Post-operative Ocular Inflammation and Pain):
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Title: Real-World Safety Analysis of an Intracanalicular Dexamethasone Insert Using the
Intelligent Research in Site (IRIS) Registry
Session Title: Medications (Preoperative, Postoperative, Intraoperative)
Session Date/Times :Sunday, April 24, 2022 at1:30 PM-1:35 PM ET
Location: WEWCC, Level 1, 143C
Presenter: Robert T Chang, MD, ABO -
Title: Real-World Characteristics of Patients Treated with Intracanalicular Dexamethasone Insert: An IRIS Registry Analysis 2019-2021
Session Title: Medications (Preoperative, Postoperative, Intraoperative)
Session Date/Times :Sunday, April 24, 2022 at1:43 PM-1:48 PM ET
Location: WEWCC, Level 1, 143C
Presenter:Michael Mbagwu , MD
DEXTENZA (Allergic Conjunctivitis):
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Title: Effects of Punctal Occlusion on Ocular Itching and Conjunctival Redness in Subjects with Allergic Conjunctivitis
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at8:28 AM-8:33 AM ET
Location: WEWCC, Level 1, 143A
Presenter:Steven M. Silverstein , MD, FACS, ABO -
Title: Sustained 30 Day Effect of an Intracanalicular Dexamethasone Insert for Treating Ocular Itching Associated with Allergic Conjunctivitis
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at8:33 AM-8:38 AM ET
Location: WEWCC, Level 1, 143A
Presenter:Steven M. Silverstein , MD, FACS, ABO -
Title: Real-World Allergic Conjunctivitis Treatment Patterns of Eye Care Providers
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at8:51 AM-8:56 AM ET
Location: WEWCC, Level 1, 143A
Presenter:William C. Christie , MD, ABO -
Title:
Patient Journey for Allergic Conjunctivitis and Initial Management
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at8:56 AM-9:01 AM ET
Location: WEWCC, Level 1, 143A
Presenter:Nandini Venkateswaran , MD, ABO
OTX-DED (dexamethasone intracanalicular insert) (Dry Eye Disease):
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Title: Safety and Efficacy of OTX-DED, an Intracanalicular Dexamethasone Insert, for the Treatment of Episodic Dry Eye Disease: A Phase 2 Study
Session Title: Ocular Surface Disease III
Session Date/Times :Saturday April 23, 2022 at3:30 PM-3:35 PM ET
Location: WEWCC, Level 1, 144B
Presenter:Lisa M. Nijm , MD, JD, ABO
Investigator-Initiated Trials Presented at ASCRS:
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Title: Thermal Pulsation with or without Dexamethasone Intracanalicular Insert for Meibomian Gland Dysfunction: A Prospective, Masked Trial
Session Title: ASCRS Electronic Posters (On-Demand)
Presenter:Paul Cacchillo , MD -
Title: A Prospective, Randomized, Fellow Eye-Controlled Study of Post-Op Pain and Inflammation Control with DEXTENZA Insert Following SMILE
Session Title: ASCRS Electronic Posters (On-Demand)
Presenter:William F. Wiley , MD -
Title: Dexamethasone Intracanalicular Insert at the Time of Surgery VS 4 Days Before for Combined Phaco and Trabecular Microbypass Implantation
Session Title: ASCRS Electronic Posters (On-Demand)
Presenter:Damien Goldberg , MD -
Title: Prospective Study of Dexamethasone Ophthalmic Insert following Concomitant MIGS and Cataract Surgery
Session Title: ASCRS LIVE Posters
Session Date/Times :Sunday, April 24, 2022 at3.10 PM -3:15 PM ET
Location:Poster Pavilion ,West Salon
Presenter:Nicholas E. Tan , BA -
Title: Intracanalicular Dexamethasone for Post-Corneal Cross-Linking Inflammation and Pain
Session Title: Keratoconus
Session Date/Times :Saturday, April 23, 2022 at8:00 AM-8:05 AM ET
Location: WEWCC, Level 1, 143C
Presenter:Alanna S. Nattis , DO -
Title: Efficacy of a Dexamethasone Intracanalicular Insert (OTX-DED), Compared to Loteprednol Suspension for the Treatment of Episodic Dry Eye
Session Title: Ocular Surface Disease II
Session Date/Times :Sunday, April 24, 2022 at8:00 AM-8:05 AM ET
Location: WEWCC, Level 1, 144A
Presenter:Andrew J. Keyser, BSc -
Title: Comparing Intracanalicular and Topical Steroid Use in Patients Undergoing Pterygium Surgery
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at8:05 AM-8:10 AM ET
Location: WEWCC, Level 1, 143A
Presenter:Michelle K. Rhee , MD, ABO -
Title: Intracanalicular Dexamethasone Insert Versus Topical Steroid or Antihistamine Therapy for Treatment of Allergic Conjunctivitis
Session Title: Ocular Surface Disease
Session Date/Times :Monday, April 25, 2022 at9:01 AM-9:06 AM ET
Location: WEWCC, Level 1, 143A
Presenter:Shani Reich , 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 commercial launch of, and the effectiveness of and amounts applicable to reimbursement codes for, DEXTENZA; the conduct of post-approval studies of and compliance with related labeling requirements for DEXTENZA and ReSure Sealant; the Company’s sales and marketing strategy; 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, 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 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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