Aldeyra (ALDX) announced that the FDA has accepted for review the resubmitted new drug application for topical ocular reproxalap, an investigational new drug candidate, for the treatment of the signs and symptoms of dry eye disease. The FDA assigned a Prescription Drug User Fee Act target action date of December 16.
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- Aldeyra Therapeutics: Buy Rating Affirmed Amidst Promising Developments in Dry Eye Disease Treatment and Strategic Partnerships
- Aldeyra Resubmits Reproxalap NDA to FDA
