Eosinophilic Esophagitis is an indication for drug development with over 30 pipeline drugs currently active. According to GlobalData, preregistered drugs for Eosinophilic Esophagitis have a 100% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Eosinophilic Esophagitis compared to historical 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.
Eosinophilic Esophagitis overview
Eosinophilic esophagitis is disease characterized by the presence of a large number of a special type of white blood cell, the eosinophil, that can cause inflammation in the esophagus. Symptoms include poor weight gain, abdominal pain, nausea, and vomiting; coughing; heartburn; and chest pain. Risk factors include weakened immune system, chemotherapy, aspirin and anti-inflammatory medications, chronic vomiting, obesity, and alcohol or cigarette use. Treatment includes antivirals, antifungals, and pain relievers.
For a complete picture of PTSR and LoA scores for drugs in Eosinophilic Esophagitis, 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.
