Alcon's Simbrinza® approved in the EU to treat patients living with glaucoma, a chronic sight-threatening eye disease - Seite 2

"Based on the literature, up to 80%[5] of patients deviate from their treatment regimen, resulting in poor adherence and the increased risk of progressive vision loss", said Professor Barbara Cvenkel, MD, Head of Glaucoma Unit, Eye Hospital Ljubljana, Slovenia and member of the Executive Committee of the European Glaucoma Society (EGS). "When appropriate, the EGS recommends the use of combination therapies, such as Simbrinza^®, which provides a less complicated administration routine by decreasing the number of eye drops to handle and reducing the treatment burden for patients affected by this eye disease."

The safety and efficacy of Simbrinza is based on two, pivotal six-month Phase III studies evaluating the safety and efficacy of Simbrinza administered twice daily, and enrolled a total of 1,450 patients with open-angle glaucoma or ocular hypertension who were insufficiently controlled on monotherapy or were already using multiple IOP-lowering medications. The primary endpoint for both studies was an assessment of mean diurnal IOP change from baseline at three months, with safety and supportive efficacy evaluated through six months. Both studies met their primary endpoints.[1]

In clinical studies, the most frequently reported adverse drug reactions in patients treated with Simbrinza were ocular hyperemia and ocular allergic type reactions.[1] The safety profile of brinzolamide 10 mg/mL and brimonidine tartrate 2 mg/mL eye drops suspension dosed twice daily (brinzolamide/brimonidine) was similar to that of the individual components and did not result in additional risk to patients relative to the known risks of the individual components.

The results of these two studies will be presented at the 32^nd Congress of the European Society of Cataract and Refractive Surgeons (ESCRS) in London, UK, on September 13-17, 2014 and during the ESCRS Glaucoma Day Programme on September 12, 2014.

The launch of Simbrinza in the EU will start in the UK in the third quarter of 2014, followed by other European markets later in 2014 and in 2015. In the US, Simbrinza was approved by the US Food and Drug Administration (FDA) and has been available in the market since 2013.

About Glaucoma
Glaucoma is the second cause of blindness after cataract and affects more than 60 million people worldwide.[6],[3],[7] Glaucoma is a group of eye diseases that lead to progressive damage of the optic nerve[8] and can result in gradual, irreversible loss of vision and eventually blindness.[9] There is no cure for glaucoma and vision lost cannot be restored. Medications can lower eye pressure[10], the only known modifiable risk factor for glaucoma[11], but must be taken life-long and regularly.[8] The exact cause of glaucoma is unknown.