ALDX
NASDAQAldeyra Therapeutics Inc.
Price$1.60-3.14 (-66.21%)
2026-01-202026-04-23
News · 26 weeks23-50%
2025-10-262026-04-19
Mix1390d
- SEC Filings5(38%)
- Other4(31%)
- Insider3(23%)
- Analyst1(8%)
Latest news
25 items- SECAldeyra Therapeutics Inc. filed SEC Form 8-K: Leadership Update8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- SECSEC Form 8-K filed by Aldeyra Therapeutics Inc.8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- INSIDERSEC Form 4 filed by Brady Todd C4 - Aldeyra Therapeutics, Inc. (0001341235) (Issuer)
- SECAmendment: SEC Form SCHEDULE 13G/A filed by Aldeyra Therapeutics Inc.SCHEDULE 13G/A - Aldeyra Therapeutics, Inc. (0001341235) (Subject)
- INSIDERSEC Form 4 filed by Douglas Richard4 - Aldeyra Therapeutics, Inc. (0001341235) (Issuer)
- INSIDERSEC Form 4 filed by Alfieri Michael4 - Aldeyra Therapeutics, Inc. (0001341235) (Issuer)
- ANALYSTAldeyra Therapeutics downgraded by H.C. Wainwright with a new price targetH.C. Wainwright downgraded Aldeyra Therapeutics from Buy to Neutral and set a new price target of $2.00
- SECAldeyra Therapeutics Inc. filed SEC Form 8-K: Regulation FD Disclosure8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- PRAldeyra Therapeutics Receives Complete Response Letter from the U.S. Food and Drug Administration for the Reproxalap New Drug Application for the Treatment of Signs and Symptoms of Dry Eye DiseaseAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced receipt of a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) for the New Drug Application (NDA) of reproxalap, an investigational drug candidate, for the treatment of dry eye disease. The CRL stated that there is "a lack of substantial evidence consisting of adequate and well-controlled investigations … that the drug product will have the effect it purports or is represented to have under the conditions of use prescribed, recommended, or suggested in its proposed labe
- SECSEC Form S-8 filed by Aldeyra Therapeutics Inc.S-8 - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- SECSEC Form 10-K filed by Aldeyra Therapeutics Inc.10-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- PRAldeyra Therapeutics to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences ConferenceAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced that Todd C. Brady, M.D., Ph.D., President and Chief Executive Officer, will participate virtually in a fireside chat at the Oppenheimer 36th Annual Healthcare Life Sciences Conference. Dr. Brady's conversation with Andreas Argyrides, Managing Director, Senior Biotech Analyst at Oppenheimer & Co. Inc., is scheduled to begin at 10:40 a.m. ET Wednesday, February 25, 2026. To view the live webcast, log in to the Investors & Media section of the Aldeyra website at https://ir.aldeyra.com. Following the
- SECAmendment: SEC Form SCHEDULE 13G/A filed by Aldeyra Therapeutics Inc.SCHEDULE 13G/A - Aldeyra Therapeutics, Inc. (0001341235) (Subject)
- SECSEC Form 8-K filed by Aldeyra Therapeutics Inc.8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- SECAldeyra Therapeutics Inc. filed SEC Form 8-K: Regulation FD Disclosure, Other Events, Financial Statements and Exhibits8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- PRAldeyra Therapeutics Announces PDUFA Extension of the New Drug Application of Reproxalap for the Treatment of Dry Eye DiseaseAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced that the U.S. Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) target action date for the reproxalap New Drug Application (NDA) for the treatment of dry eye disease. The extended PDUFA target action date is March 16, 2026. Following submission on June 16, 2025, the NDA was accepted for review as a "complete class 2 response" by the FDA on July 16, 2025, with a target PDUFA action date of December 16, 2025. On December 12, 2025, the FDA met with Aldeyra to r
- SECAmendment: SEC Form SCHEDULE 13G/A filed by Aldeyra Therapeutics Inc.SCHEDULE 13G/A - Aldeyra Therapeutics, Inc. (0001341235) (Subject)
- SECAldeyra Therapeutics Inc. filed SEC Form 8-K: Regulation FD Disclosure, Other Events, Financial Statements and Exhibits8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- PRAldeyra Therapeutics Announces Expansion of RASP Platform to Include Central Nervous System Diseases and Provides Updates on Reproxalap at Research & Development WebcastAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced at a research and development webcast the expansion of the RASP platform to include programs in central nervous system diseases associated with inflammation, and provided updated manufacturing information on reproxalap. Based on new preclinical results in models of Parkinson's disease and amyotrophic lateral sclerosis, which included improved grip strength, balance, and biomarkers of central nervous system function, potential clinical indications for the orally administered, next-generation RASP
- PRAldeyra Therapeutics to Participate in the Jefferies Global Healthcare Conference in LondonAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced that Todd C. Brady, M.D., Ph.D., President and Chief Executive Officer, will participate in a fireside chat at the 2025 Jefferies Global Healthcare Conference in London, England. Dr. Brady's conversation with Clara Dong, Ph.D., Vice President, Biotechnology Equity Research at Jefferies LLC., is scheduled to begin at 11:30 a.m. GMT Thursday, November 20, 2025. To view the live webcast, log in to the Investors & Media section of the Aldeyra website at https://ir.aldeyra.com. Following the fireside c
- SECSEC Form 10-Q filed by Aldeyra Therapeutics Inc.10-Q - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- SECAldeyra Therapeutics Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits8-K - Aldeyra Therapeutics, Inc. (0001341235) (Filer)
- PRAldeyra Therapeutics Announces Positive Results from Phase 2 Clinical Trial in Alcohol-Associated Hepatitis, Focuses RASP Product Candidate Pipeline on Next-Generation MoleculesRelative to Baseline, Signal-Finding Molecule ADX‑629 Demonstrated Statistically Significant Improvement in Liver Function in Patients with Alcohol-Associated Hepatitis RASP Modulator Product Candidate Pipeline Focused on ADX‑248 and ADX‑246 for Dermatologic, Metabolic, and Retinal Immune-Mediated Diseases Cash Runway Extended into the Second Half of 2027 Aldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated diseases, today announced achievement of statistically significant improvement in liver function in patients treated with ADX-629, an investigational new drug can
- PRAldeyra Therapeutics to Participate in the H.C. Wainwright 27th Annual Global Investment ConferenceAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat immune-mediated and metabolic diseases, today announced that Todd C. Brady, M.D., Ph.D., President and Chief Executive Officer, will participate in a fireside chat at the H.C. Wainwright 27th Annual Global Investment Conference on September 8, 2025. Dr. Brady's conversation with Matthew Caufield, Director, Equity Research at H.C. Wainwright & Co., is scheduled to begin at 11:30 a.m. ET Monday, September 8, 2025. To view the live webcast, log in to the Investors & Media section of the Aldeyra website at https://ir.aldeyra.com. Following th
- PRAldeyra Therapeutics Receives Orphan Designation from the European Medicines Agency for ADX-2191 for the Treatment of Primary Large B-Cell Lymphomas of Immune-Privileged Sites, including Primary Vitreoretinal LymphomaAldeyra Therapeutics, Inc. (NASDAQ:ALDX) (Aldeyra) today announced that the European Medicines Agency (EMA) has granted Orphan Designation for ADX-2191 (methotrexate intravitreal injection, USP) for the treatment of primary large B-Cell lymphomas of immune-privileged sites, including primary vitreoretinal lymphoma. There is currently no approved treatment for patients with primary vitreoretinal lymphoma, a rare, aggressive, high-grade cancer that affects approximately 100 to 200 people per year in the European Union. "Primary vitreoretinal lymphoma is a potentially fatal cancer that today is treated with off-label compounded formulations of methotrexate that are injected into the eye," st