Post-cataract surgery intraocular injections offer alternative to traditional drop therapy

With more than 3 million procedures performed annually in the U.S., cataract surgery is nearly a rite of passage. Technological advances including phacoemulsification and premium IOLs have all contributed to making cataract surgery one of the safest and most effective procedures performed. However, the post-surgical drop regimen has remained a largely unchanged and cumbersome process for both patients and office staff.As an “in the trenches” surgeon working to provide the best care for my patients, I believe the time has arrived to confidently adopt the practice of administering post-surgical pharmacological treatment intraocularly. Patients benefit from the convenience and affordability, and my staff is relieved of many of the calls we receive from patients and pharmacies. To best serve the needs of my patients, I adopted Tri-Moxi-Vanc therapy (Imprimis Pharmaceuticals) into my surgical armamentarium. The compounded medication consists of a proprietary formulation of triamcinolone acetonide, moxifloxacin hydrochloride and vancomycin in a sterile package. The product is ordered from an accredited compounding pharmacy and delivered directly to the office.

Fallout from failed clinical trials poses challenges to companies

So far in 2015, four different ophthalmic products in phase 3 clinical trials failed to meet their primary endpoints. Ocular Surgery News spoke with three of these companies to find out what happened and how they responded. Their stories offer a telling glimpse at the challenges and opportunities companies face when endpoints are missed in clinical trials as part of the overall innovation cycle.“Private companies often simply learn from their experience and make appropriate adjustments to their research and business plan. They continue on as long as their investors are optimistic they will eventually create value,” OSN Chief Medical Editor Richard L. Lindstrom, MD, said. “Public companies must disclose any material event in a timely fashion and usually see a significant fall in their share price, usually in the 20% to 50% range, but it can be even more if it is an FDA trial not approved by a panel.”