
FDA Extends Review Timeline For Aldeyra's Dry Eye Disease Drug

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The FDA has extended the review timeline for Aldeyra Therapeutics' dry eye disease drug, reproxalap, to March 16, 2026, following a major NDA amendment. The amendment was due to new clinical study report data. Aldeyra's stock fell 12.1% after the announcement, with further decline in premarket trading. The FDA plans to communicate labeling requests by February 2026 if no major deficiencies are found.
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