Eton Pharmaceuticals (ETON) announced positive results from bioequivalence study of ET-600, a patented oral solution of desmopressin under development for the treatment of central diabetes insipidus. In a bioequivalence study conducted in 75 human subjects, ET-600 showed pharmacokinetic equivalence to the FDA-approved reference product of the same active ingredient.
"We expect to submit the NDA shortly and have begun pre-launch commercial readiness activities in anticipation of a potential launch in the first quarter of 2026," said Sean Brynjelsen, CEO of Eton Pharmaceuticals.
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