TGI-2 is under clinical development by Hefei TG ImmunoPharma and currently in Phase I for Metastatic Ovarian Cancer. According to GlobalData, Phase I drugs for Metastatic Ovarian Cancer have a 77% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how TGI-2’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
Smarter leaders trust GlobalData
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.
TGI-2 overview
TGI-2 (NM1F) is under development for the treatment of advanced, or metastatic solid tumors, including metastatic ovarian cancer, metastatic melanoma, triple negative breast cancer and metastatic colorectal cancer. The drug candidate is administered through parenteral route. It acts by targeting poliovirus receptor-related immunoglobulin domain-containing (PVRIG) and is being developed based on ABC-NKer platform.
Hefei TG ImmunoPharma overview
Hefei TG ImmunoPharma formerly (Hefei Tiangang Immune Drug Co Ltd) is engaged in the field of tumor immunotherapy that intends to use the proceeds to advance the development and registration of multiple product pipelines for tumor immunotherapy. The company is headquartered in Hefei, China.
For a complete picture of TGI-2’s drug-specific PTSR and LoA scores, buy the report here.
Data 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, 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.
