Mosedipimod is under clinical development by Enzychem Lifesciences and currently in Phase II for Chemotherapy Induced Oral Mucositis. According to GlobalData, Phase II drugs for Chemotherapy Induced Oral Mucositis does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Mosedipimod LoA Report. 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.

Mosedipimod overview

Mosedipimod (EC-18) is under development for the treatment of acute radiation syndrome, sepsis, rheumatoid arthritis, asthma, nonalcoholic steatohepatitis, liver fibrosis, chronic obstructive pulmonary disease, psoriasis, atopic dermatitis, mustard gas (sulfur mustard) poisoning, chemotherapy induced oral mucositis and coronavirus disease 2019 (Covid-19) pneumonia, coronavirus disease 2019 (Covid-19) associated acute respiratory distress syndrome. It is administered through oral route as capsule. The drug candidate is a monoacetyldiacylglyceride derived from deer antlers. It is developed based on lipid medicine platform technology. The drug candidate was also under development for the treatment of biliary cancer. It was also under development for chemotherapy induced neutropenia (CIN) including febrile and afebrile neutropenia

Enzychem Lifesciences overview

Enzychem Lifesciences (Enzychem) develops and produces novel drugs and active pharmaceutical ingredients (APIs). The company is developing new drugs to treat diseases like asthma, psoriasis, rheumatoid arthritis, atopic dermatitis, acute radiation syndrome, sepsis, and autoimmune disorders. The company’s pipeline product EC-18, is being developed for the treatment of cancer and inflammation. Enzychem servers the patients across the globe. It has research and development center in Chungcheongbuk-do, South Korea. The company has its operations in South korea and the USA. The company is headquartered in Seocho-gu, Seoul, South Korea.

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

This content was updated on 20 February 2024

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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.