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Ocular Therapeutix Begins Phase 3 Clinical Trial for its Sustained Release Dexamethasone

Companies mentioned in this article: Ocular Therapeutix, Inc.

BEDFORD, Mass. -- (BUSINESS WIRE) -- Ocular Therapeutix, Inc. announces the start of its Phase 3 clinical program to evaluate the safety and efficacy of their sustained release dexamethasone, an ophthalmic corticosteroid for the treatment of post-operative inflammation and pain following cataract surgery. Ocular Therapeutix’s dexamethasone is administered as a one-time, bioabsorbable intracanalicular plug for release of the steroid to the ocular surface for up 30 days.

In the first of two prospective, multicenter, randomized, parallel-arm, double-masked, vehicle-controlled studies, 240 patients undergoing clear corneal cataract surgery will be enrolled at sites throughout the United States. Following surgery, patients will be randomized to either the dexamethasone treatment group or a placebo vehicle plug. Primary endpoints are absence of anterior chamber cells at day 14 and reduction of pain at day 8. “The dexamethasone plug is easily inserted in the operating room immediately following cataract surgery,” stated Thomas Walters, MD, of Texan Eye in Austin, Texas. “In the earlier Phase 2 clinical trial, it proved effective for relieving pain and inflammation, and patients were comfortable with use of the plug.”

Physicians routinely prescribe topical steroids post-operatively for the treatment of ocular inflammation and pain. However, patients do not reliably self-administer these drops, which could lead to greater or more persistent inflammation and subsequently affect visual outcomes. Conversely, chronic use of topical steroids can lead to elevations in intraocular pressure, which is a risk factor for glaucoma. “A single-dose corticosteroid can help manage issues of compliance by putting dosing into the hands of the physician and avoiding up to four drops per day and a tapering regimen which is confusing for the patient,” stated Amar Sawhney, Ph.D., President and CEO of Ocular Therapeutix, Inc. “We look forward to the completion of this trial, and continuing on to the second Phase 3 trial later this year.”

About Ocular Therapeutix’s Intracanalicular Plugs:
Ocular Therapeutix is developing the company’s proprietary absorbable polyethylene glycol hydrogel intracanalicular plug technology to release drugs in a sustained fashion over a specified period of time depending on the drug and its corresponding therapeutic need. At the end of the treatment period, the plug is designed to absorb, and exit the nasolacrimal system without need for removal by the physician. The plugs contain a visualization agent for retention monitoring throughout the treatment period.

About Ocular Therapeutix, Inc.:
Ocular Therapeutix, Inc. is a privately held company based in Bedford, MA, focused on the development and commercialization of ophthalmic therapeutic products using its proprietary hydrogel technology. Ocular Therapeutix’s first product, the ReSure Sealant, was FDA approved in January 2014 for the prevention of post-operative fluid egress following cataract surgery. Ocular Therapeutix is in clinical trials for drug-eluting intracanalicular plugs for both treatment of post-operative pain and inflammation and glaucoma, and is developing sustained release injectable anti-VEGF drug depots for back-of-the-eye diseases.

Forward-Looking Statements:
Any statements in this news release about future expectations, plans and prospects for Ocular Therapeutix constitute forward-looking statements. Actual results may differ materially from those indicated by such forward-looking statements. Ocular Therapeutix anticipates that subsequent events and developments may cause its views to change. However, while Ocular Therapeutix may elect to update these forward-looking statements in the future, it specifically disclaims any obligation to do so.


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Contact:

Ocular Therapeutix, Inc.
Scott Corning, 781-357-4000
Vice President of Sales and Marketing
scorning@ocutx.com