Aldeyra Therapeutics Seeks FDA Clarification on Reproxalap NDA Meeting Minutes

MT Newswires Live

07/16

Aldeyra Therapeutics (ALDX) said Thursday it received meeting minutes from the US Food and Drug Administration regarding the potential resubmission of its new drug application for reproxalap to treat dry eye disease.

The company requested clarification of the meeting minutes from the FDA and plans to seek a Type D meeting to discuss the potential NDA resubmission.

Aldeyra expects the Type D meeting to be held by the end of Q3 2026, it added.

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