Danburstotug is under clinical development by ImmuneOncia Therapeutics and currently in Phase II for Hepatocellular Carcinoma. According to GlobalData, Phase II drugs for Hepatocellular Carcinoma have a 33% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Danburstotug’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.

Danburstotug overview

STIA-1015 is under development for the treatment of solid tumors including colon cancer, gastric adenocarcinoma, esophageal squamous cell carcinoma, advanced urothelial carcinoma, in-transit metastatic melanoma, hepatocellular carcinoma and relapsed or refractory extranodal NK/T Cell Lymphoma. It is administered through intravenous and intralymphatic route. The drug candidate is a monoclonal antibody targeting PD-L1 (programmed cell death 1 ligand 1).

ImmuneOncia Therapeutics overview

ImmuneOncia Therapeutics Inc, an immuno-oncology-centric biopharmaceutical company that is engaged in drug development and antibody engineering. The company is headquartered in Seongnam, Gyeonggi, South Korea.

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

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 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.