Eton Pharmaceuticals develops and commercializes treatments for rare diseases, with commercial products that include KHINDIVI, INCRELEX, ALKINDI SPRINKLE, DESMODA, GALZIN, HEMANGEOL, PKU GOLIKE, Carglumic Acid, Betaine Anhydrous and Nitisinone. Company news commonly covers FDA approvals, product launches, licensing of U.S. commercialization rights, specialty pharmacy distribution and Eton Cares patient-support programs.
Updates also address financial results, product-sales trends, late-stage product candidates and clinical work for rare-disease therapies. Pipeline references include Amglidia, ET-700, ET-800 and ZENEO hydrocortisone autoinjector, with ET-700 described as an extended-release zinc acetate formulation for Wilson disease.
Eton Pharmaceuticals, Inc. (Nasdaq: ETON) has been confirmed as the first filer of an Abbreviated New Drug Application (ANDA) for cysteine hydrochloride injection, referencing Exela Pharma Sciences' Elcys. Eton plans to challenge the validity of Exela's patents in the U.S. Patent & Trademark Office, aiming for a potential product launch in November 2021 if successful. The cysteine injection market is valued at over $50 million annually, and Eton aims to provide a lower-cost alternative to patients.
Eton Pharmaceuticals, Inc. (Nasdaq: ETON) will report its first quarter 2020 financial and operational results on May 14, 2020. A conference call and audio webcast will follow at 4:30 p.m. ET. Investors can access the live webcast on Eton's investor website or by calling specified numbers. Eton specializes in developing innovative drug products, focusing on hospital injectable and pediatric rare disease products. Its initial product, Biorphen, is the only FDA-approved ready-to-use phenylephrine injection, launched in December 2019. The lead pediatric product, Alkindi® Sprinkle, is currently under FDA review.