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Aldeyra Therapeutics (ALDX) Announces Positive Top-Line Results from 12-Month Safety Clinical Trial of Reproxalap in Patients with Dry Eye Disease

Aldeyra Therapeutics (ALDX) Announces Positive Top-Line Results from 12-Month Safety Clinical Trial of Reproxalap in Patients with Dry Eye Disease
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Eastern Virginia Medical School , United States , John Sheppard , Ptoddc Brady , Aldeyra Therapeutics Inc , Molecular Biology At Eastern Virginia Medical School , Chief Executive Officer , Virginia Eye Consultants , Molecular Biology , Eastern Virginia Medical ,

Aldeyra Therapeutics Announces Next-Generation RASP-Modulator Drug Candidates Expected to Begin Clinical Trials for Systemic Immune-Mediated Diseases and Geographic Atrophy

Aldeyra Therapeutics Announces Next-Generation RASP-Modulator Drug Candidates Expected to Begin Clinical Trials for Systemic Immune-Mediated Diseases and Geographic Atrophy
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United States , Scott Solomon , Ptoddc Brady , Sharon Merrill Associates Inc , Drug Administration Investigational New , Drug Administration New Application , Lancet Global Health , Exchange Commission , Aldeyra Therapeutics Inc , Development Engine Targeting , Securities Exchange , Systemic Immune Mediated Diseases , Geographic Atrophy Build , Drug Discovery , Product Candidates Highlight Aldeyra , Clinical Indication Expansion , Retinal Diseases Characterized , Chief Executive Officer , Private Securities Litigation Reform Act , Securities Exchange Act , Financial Condition , Annual Report , Quarterly Report , Media Contact , Merrill Associates , Aldeyra Therapeutics ,

Aldeyra Therapeutics (ALDX) to Begin ADX‑246 and ADX‑248 Trials for Systemic Immune-Mediated Diseases and Geographic Atrophy

Aldeyra Therapeutics (ALDX) to Begin ADX‑246 and ADX‑248 Trials for Systemic Immune-Mediated Diseases and Geographic Atrophy
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Reproxalap, a First-in-Class RASP Modulator, Under Review for Dry Eye Disease

The FDA has accepted the NDA for reproxalap for the treatment of dry eye disease. ....

Ptoddc Brady , Drug Administration , New Drug Application , Prescription Drug User Fee Act , Accessed February ,

Aldeyra Therapeutics Submits New Drug Application to the U.S. Food and Drug Administration for ADX‑2191 for the Treatment of Primary Vitreoretinal Lymphoma

Aldeyra Therapeutics Submits New Drug Application to the U.S. Food and Drug Administration for ADX‑2191 for the Treatment of Primary Vitreoretinal Lymphoma
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