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A new study of over 47,000 women found links between coffee drinking and healthy aging. Here’s what we know.
Once commenced, the bioequivalence study is relatively short, scheduled for less than 30 days from start to finish.
Once commenced, the bioequivalence study is relatively short, scheduled for less than 30 days from start to finish.
Once commenced, the bioequivalence study is relatively short, scheduled for less than 30 days from start to finish. The Company plans to make further updates in the coming weeks regarding its ...
Eton Pharmaceuticals, Inc (Eton), an innovative pharmaceutical company focused on developing and commercializing treatments for rare diseases, announced positive results from its bioequivalence study ...
(RTTNews) - 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 ...
Eton Pharmaceuticals reports successful bioequivalence of ET-600 and plans NDA submission in April 2025 for diabetes insipidus treatment.
Eton Pharmaceuticals (ETON) announced positive results from its bioequivalence study of ET-600, a proprietary, patented oral solution of desmopressin under development for the treatment of central ...
- Company's patented desmopressin oral solution successfully passed pivotal bioequivalence study - - Company expects to submit New Drug Application (NDA) in April 2025 - DEER PARK, Ill., March 14, ...
Subsequently, the developed methodology was applied in a bioequivalence study involving anemia patients. The in-study quality control results demonstrated that the method was highly accurate, with ...
The publication, entitled, "Two-Way Randomized Crossover Study to Establish Pharmacodynamic Bioequivalence Between Oxylanthanum Carbonate and Lanthanum Carbonate” described the study that established ...