Abelacimab is under clinical development by Anthos Therapeutics and currently in Phase III for Atrial Fibrillation. According to GlobalData, Phase III drugs for Atrial Fibrillation have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Abelacimab’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.

Abelacimab overview

Abelacimab is under development for the prevention of arterial and venous thrombosis, venous thromboembolism (VTE), pulmonary embolism, deep vein thrombosis, inflammation and stroke and systemic embolism in patients with atrial fibrillation. The therapeutic candidate is an anti-FXI monoclonal antibody and is a new molecular entity. It acts by targeting coagulation factor XI. It is administered through subcutaneous and intravenous routes.

Anthos Therapeutics overview

Anthos Therapeutics is a healthcare company engaged in the research and development of genetically and pharmacologically validated therapies for cardiovascular and metabolic (CVM) diseases. The company is headquartered in Cambridge, Massachusetts, the US.

For a complete picture of Abelacimab’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.