RC-402 is under clinical development by Virocure and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how RC-402’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.

RC-402 overview

RC-402 is under development for the treatment of advanced malignant solid tumors including melanoma, gastric adenocarcinoma, gastro oesophageal junction adenocarcinoma, gastrointestinal stromal tumors, colon cancer and lung cancer. It is an oncolytic virus-based therapy. It is administered through intratumor route.

Virocure overview

Virocure is a Pharmaceuticals and Healthcare company that provides treatment for Cancer. The company is Headquartered in Gurodong, Seoul, Republic of Korea (South Korea).

For a complete picture of RC-402’s drug-specific PTSR and LoA scores, buy the report here.


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.