Levi & Korsinsky said it has opened an investigation into Aldeyra Therapeutics over potential violations of U.S. federal securities laws. The firm is reviewing Aldeyra’s 2024 and 2025 statements about the development and regulatory prospects of reproxalap for dry eye disease. It cited an FDA Complete Response Letter dated March 17, 2026 stating that reproxalap had not demonstrated sufficient efficacy. The investigation is examining whether Aldeyra failed to disclose material information about efficacy risks.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Aldeyra Therapeutics Inc. published the original content used to generate this news brief via Newsfile (Ref. ID: 202603181234NEWSFILECNPR____20260318_289022_1) on March 18, 2026, and is solely responsible for the information contained therein.
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