US FDA snubs Avedro's drug-device treatment for rare eye conditions
This article was originally published in Clinica
Executive Summary
The US FDA has rejected Avedro’s approval application for its riboflavin ophthalmic solution/KXL System, which the company has been developing for keratoconus, a rare potentially blinding disease, and corneal ectasia, a rare outcome of refractive surgery, such as LASIK.
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