ASC-618 is under clinical development by ASC Therapeutics and currently in Phase II for Hemophilia A (Factor VIII Deficiency). According to GlobalData, Phase II drugs for Hemophilia A (Factor VIII Deficiency) have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how ASC-618’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.

ASC-618 overview

ASC-618 is under development for hemophilia A. The drug candidate is developed based on CRISPR/Cas9 genome editing technology, TARGATT and coagulation factor VIII expression technologies. It is administered through intravenous route. The drug candidate acts by targeting coagulation factor VIII. The gene is delivered using adeno-associated virus (AAV) vector.

ASC Therapeutics overview

ASC Therapeutics is a biotechnology company which is engaged in research and development of cure for intractable and rare diseases using gene and cell therapy. It is headquartered in Milpitas, California, the US.

For a complete picture of ASC-618’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 20 February 2024

Premium 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.