ASC-60 is under clinical development by Sagimet Biosciences and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 69% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ASC-60’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-60 overview
TVB-3567 is under development for the treatment of respiratory syncytial virus (RSV) infections, hepatitis, rhinovirus infection, parainfluenza virus 3 (PIV3) infections, severe acute respiratory syndrome virus, solid tumors and acne. It is administered through oral route. The drug candidate is a small molecule and acts by targeting fatty acid synthase.
Sagimet Biosciences overview
Sagimet Biosciences is a clinical-stage pharmaceutical company that develops novel therapeutics in metabolic diseases. It offers TVB-2640, a fatty acid synthase inhibitor used for the treatment of solid tumors, including non-small cell lung cancer (NSCLC), breast cancer and ovarian cancer. The company’s pipeline program includes fatty acid synthase inhibitors and a research platform in the treatment of solid tumors. Sagimet Biosciences provides an FASN inhibitor, an essential enzyme that is responsible for the synthesis of palmitic acid and used in tumor metabolism, tumor cell survival and lipid signaling. The company develops antiviral therapeutic candidates for respiratory syncytial virus, cytomegalovirus, and other human pathogens. Sagimet Biosciences is headquartered in San Mateo, California, the US.
For a complete picture of ASC-60’s drug-specific PTSR and LoA scores, buy the report here.
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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.
