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Eyenovia and Formosa Pharma Launch FDA-Approved APP13007 for Postoperative Ocular Inflammation

• Eyenovia and Formosa Pharmaceuticals have launched APP13007 (clobetasol propionate ophthalmic suspension, 0.05%) for postoperative inflammation and pain, the first FDA-approved ophthalmic drug using clobetasol propionate. • The U.S. ophthalmic steroid market is valued at $1.3 billion, with nearly seven million surgeries performed annually, highlighting the potential impact of APP13007. • APP13007's twice-daily dosing offers a more convenient and cost-effective option compared to other treatments requiring up to four doses per day. • Eyenovia is initiating full-scale commercialization of APP13007 in September 2024, following Formosa Pharmaceuticals' initial shipment to the U.S.

Eyenovia Inc. and Formosa Pharmaceuticals have announced the launch of APP13007 (clobetasol propionate ophthalmic suspension, 0.05%), a novel, FDA-approved ophthalmic drug designed to treat postoperative inflammation and pain following eye surgery. This collaboration marks a significant advancement in ocular therapeutics, leveraging Formosa's APNT nanotechnology platform.
The U.S. ophthalmic steroid market is substantial, valued at approximately $1.3 billion, with nearly seven million ophthalmic surgeries conducted each year. APP13007 distinguishes itself through its unique formulation and twice-daily dosing regimen, offering a potentially more convenient and cost-effective alternative to existing treatments that often require up to four doses daily.

Clinical Advantages of APP13007

APP13007 is the first FDA-approved ophthalmic drug to utilize clobetasol propionate, a super-potent corticosteroid. Its formulation is specifically designed to address the inflammation and pain associated with postoperative recovery in ocular surgery patients. The twice-daily dosing regimen enhances patient compliance and reduces the burden of frequent administration, a common challenge with other ophthalmic steroids.

Commercialization and Market Impact

Formosa Pharmaceuticals has already shipped the initial supply of APP13007 to the U.S. to facilitate commercialization. Eyenovia is set to begin full-scale commercial operations in September 2024. The launch is supported by pre-launch activities aimed at establishing a strong market presence in the competitive ophthalmic sector. Investors and analysts speculate that the successful market entry of APP13007 could significantly boost Eyenovia's revenues and overall market position.

About Clobetasol Propionate

Clobetasol propionate is a highly potent corticosteroid known for its anti-inflammatory and immunosuppressive properties. In the context of postoperative eye care, it effectively reduces inflammation, edema, and associated pain, thereby promoting faster and more comfortable recovery for patients undergoing ophthalmic surgeries.
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[1]
EYEN Shares Are Trading Higher Today: What You Need To Know - Benzinga
benzinga.com · Sep 9, 2024

Eyenovia Inc (EYEN) shares surge due to the launch of FDA-approved ophthalmic drug APP13007, developed with Formosa Phar...

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