EC-5026 is under clinical development by Eicosis and currently in Phase I for Inflammatory Pain. According to GlobalData, Phase I drugs for Inflammatory Pain have an 81% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how EC-5026’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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.
EC-5026 overview
EC-5026 is under development for the treatment of diabetic neuropathic pain, arrhythmogenic cardiomyopathy, chronic pain, inflammatory pain and osteoarthritis pain. The drug candidate is administered through oral route in the form of tablet and capsule. It acts by targeting soluble epoxide hydrolase (sEH).
Eicosis overview
EicosisThe company operates in the pharmaceuticals and healthcare industry, specializing in the central nervous system therapy area. It focuses on developing treatments for disorders related to the central nervous system. The company is headquartered in Davis, California, the US.
For a complete picture of EC-5026’s drug-specific PTSR and LoA scores, buy the report here.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.
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.
