CPL-207280CA is under clinical development by Celon Pharma and currently in Phase I for Diabetic Neuropathy. According to GlobalData, Phase I drugs for Diabetic Neuropathy have an 88% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CPL-207280CA’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.

CPL-207280CA overview

CPL-207280CA is under development for the treatment of type 2 diabetes and diabetic neuropathy. It is administered through oral route in form of tablet and acts by targeting GPCR (GPR40). It was also under development for the treatment of obesity.

Celon Pharma overview

Celon Pharma a subsidiary of Glatton Sp Zoo, is a biopharmaceutical company that researches, develops, produces and distributes generic medicinal products and pharmaceutical preparations to treat cancer, diabetes, neurological and metabolic diseases. The company’s product range includes Aromek, Salmex, Valzek, Lazivir, Donepex and Ketrel. It is investigating drugs against solid tumors, neuropathic pain, asthma, autoimmune diseases, diabetes, psoriasis, Schizophrenia and drug-resistant depression among others. Celon Pharma conducts advanced scientific research and development programs to produce modern drugs. The company works in collaboration with academic and research institutions to discover new therapies. Celon Pharma is headquartered in Lomianki, Mazovia, Poland.

For a complete picture of CPL-207280CA’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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

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.