Aldeyra Therapeutics Receives Fast Track Designation for ADX‑2191 for the Treatment of Retinitis Pigmentosa
LEXINGTON, Mass.--(BUSINESS WIRE)--Aldeyra Therapeutics, Inc. (Nasdaq: ALDX) (Aldeyra) today announced that the U.S. Food and Drug Administration (FDA) has granted fast track designation for ADX-2191 (methotrexate intravitreal injection, USP) for the treatment of retinitis pigmentosa. There is currently no approved treatment for patients with most forms of retinitis pigmentosa, a clinical group of rare genetic eye diseases characterized by retinal cell death and loss of vision. Retinitis pigmen
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How will the fast‑track designation affect Aldeyra’s short‑term stock price and trading volume?
What is the anticipated timeline for clinical‑trial milestones and potential FDA approval for ADX‑2191?
How does ADX‑2191’s market potential and competitive landscape compare to other emerging retinitis pigmentosa therapies?