GC-101 is under clinical development by Shanghai Juncell Therapeutics and currently in Phase I for Cervical Cancer. According to GlobalData, Phase I drugs for Cervical Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how GC-101’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.

GC-101 overview

GC-101 is under development for the treatment of gastrointestinal tumors, epidermolysis bullosa, advanced solid tumors, metastasized breast cancer, glioma, advanced metastatic melanoma, hepatobiliary cancer,  cervical cancer, head and neck squamous cell tumors, non-small cell lung cancer, breast cancer and pancreatic cancer. It is administered through parenteral and intravenous route. The therapy comprises of autologous tumor infiltrating lymphocytes (TILs).

Shanghai Juncell Therapeutics overview

Shanghai Juncell Therapeutics specializes in research and development of tumor-infiltrating lymphocytes therapies for the treatment of solid tumors. The company is headquartered in Shanghai City. Shanghai, China.

For a complete picture of GC-101’s drug-specific PTSR and LoA scores, buy the report here.

Data Insights


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.