Isnes, Belgium (Oct 30, 2014) – iSTAR Medical SA, a privately held ophthalmic device company, announced today that the first patient in its European multi-center clinical trial has been successfully implanted with the STARflo™ glaucoma drainage device.
The study will be conducted at leading clinical study sites across Europe to evaluate the effectiveness and safety of the STARflo™ system in patients with Open-angle glaucoma and is designed to support broader adoption of STARflo™ in geographies where it has been approved. STARflo received European CE Mark approval in 2012 and is currently available through distributors in select countries.
The first implantation procedure in the clinical trial was successfully performed by Professor Christophe Baudouin, head of the Ophthalmology Department at the Quinze-Vingt National Ophthalmologic University Hospital in Paris, France.
About Glaucoma and STARflo™
Glaucoma is the leading cause of irreversible blindness worldwide. By 2020, it is estimated that 80 million people worldwide will have the disease. Elevated intraocular pressure is considered a major risk factor for glaucoma and its progression. STARflo is a non-degradable, precision-pore, implant made from STAR® Biomaterial. It is designed to operate as a bleb-free, micro-porous drainage system to reduce intraocular pressure (IOP) in patients suffering from open-angle glaucoma by augmenting the eye’s natural uveoscleral outflow.