Hydrocortisone is under clinical development by Eton Pharmaceuticals and currently in Pre-Registration for Adrenal Insufficiency. According to GlobalData, Pre-Registration drugs for Adrenal Insufficiency have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Hydrocortisone’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Hydrocortisone overview
Hydrocortisone is under development for the treatment of adrenal insufficiency. It is administered through oral route in the form of solution. It acts by targeting glucocorticoid receptor.
Eton Pharmaceuticals overview
Eton Pharmaceuticals is a pharmaceutical company. It develops and commercializes pharmaceutical products including formulations. The company’s marketed products are Alkindi Sprinkle, Betaine Anhydrous, and Carglumic Acid. Its pipeline products include dehydrated alcohol injection, ZENEO hydrocortisone autoinjector, ET-400, and ET-500. Eton Pharmaceuticals develops its products in multiple dosage forms including liquid formulations, sterile injectables, oral liquids, and ophthalmics. The company leverages relationships with development partners in the US and Europe to create a portfolio of products. The company’s products find application in therapeutic areas including endocrinology and metabolic genetics. Eton Pharmaceuticals is headquartered in Deer Park, Illinois, the US.
For a complete picture of Hydrocortisone’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
