IAP-0971 is under clinical development by Sunho (China) Biopharmaceutical and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 10% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how IAP-0971’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.

IAP-0971 overview

IAP-0971 is under development for the treatment of solid tumor, lung cancer, cervical cancer, head and neck squamous cell carcinoma, liver cancer and non-Hodgkin lymphoma. The drug candidate is administered through subcutaneous route. It acts by targeting PD1 and IL15.

Sunho (China) Biopharmaceutical overview

Sunho (China) Biopharmaceutical (Sunho (China) Biopharmaceutical) is a healthcare service provider. It specializes in developing drugs for the treatment of cancer. Sunho (China) Biopharmaceutical is headquartered in Chengdu, China.

For a complete picture of IAP-0971’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.