IMM-2902 is under clinical development by ImmuneOnco Biopharmaceuticals (Shanghai) and currently in Phase I for Gastric Cancer. According to GlobalData, Phase I drugs for Gastric Cancer have a 77% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IMM-2902’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.

IMM-2902 overview

IMM-2902 is under development for the treatment of solid tumors including HER2 positive breast cancer, stomach cancer, lung cancer, adenocarcinoma of the gastroesophageal junction, ovarian cancer, metastatic breast cancer, gastric cancer, cholangiocarcinoma, cervical cancer, cholangiocarcinoma, colon cancer, esophageal cancer, gastroesophageal junction carcinomas, colorectal cancer and non-small cell lung cancer . It is a bi-specific monoclonal antibody that acts by targeting CD47 and cells expressing tyrosine protein kinase ERBB 2 (HER2). It is administered through intravenous drip.

ImmuneOnco Biopharmaceuticals (Shanghai) overview

ImmuneOnco Biopharmaceuticals (Shanghai) is an early stage biopharmaceutical company, engaged in the production and commercialization of innovative cancer immunotherapy products with the aim of reversing cancer cell-induced immune inhibition and actively eradicating cancer cells. The company is headquartered in Shanghai, China.

For a complete picture of IMM-2902’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 7 February 2024

Premium 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.