Vanadis-01 is under clinical development by CFM Pharma and currently in Phase I for Myocardial Infarction. According to GlobalData, Phase I drugs for Myocardial Infarction have a 90% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Vanadis-01’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.

Vanadis-01 overview

Vanadis-01 is under development for the treatment of ischemic reperfusion injury in myocardial infarction patients. The therapeutic candidate contains bis-maltolato-oxo-vanadium (organic vanadium salt). It acts by targeting protein tyrosine phosphatases. It is administered through the intravenous route.

CFM Pharma overview

CFM Pharma is a pharmaceutical company that develops drugs for acute traumatic diseases and heart infarctions. The company offers solutions for heart attack, second-and third-degree burns, acute renal failure, and others. It provides service such as renal ischemia (hypotension, sepsis ), toxic causes (drugs or contrast medium), and other traumatic injuries. CFM Pharma provides Vanadis, a drug used to cure tissue damage, heart reperfusion damages, kidney injuries, and others. The company has business presence in Europe, the USA, Japan, and others. CFM Pharma is headquartered in IJsselstein, Utrecht, the Netherlands.

For a complete picture of Vanadis-01’s drug-specific PTSR and LoA scores, buy the report here.


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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.