WVU Eye Institute retinopathy of prematurity clinical trial results in FDA approval
A clinical trial conducted by the WVU Eye Institute for the use of EYELEA, an injection medication, has led to FDA approval for the treatment of retinopathy of prematurity (ROP).
By websupport@aspwv.com|2024-04-24T15:57:12-04:00April 24th, 2024|Comments Off on WVU Eye Institute retinopathy of prematurity clinical trial results in FDA approval