WATERTOWN, Mass.--(BUSINESS WIRE)--pSivida Corp. (NASDAQ: PSDV) (ASX: PVA), a leader in the development of sustained release, drug delivery products for treating eye diseases, today announced that the New Drug Application for ILUVIEN for the treatment of chronic Diabetic Macular Edema has been resubmitted to the U.S. Food and Drug Administration (FDA). In the resubmission, pSivida’s licensee, Alimera Sciences, responded to questions raised in the FDA’s October 2013 complete response letter and provided a safety update, which included commercial experience with ILUVIEN in Europe.
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