HEC-68498 is under clinical development by HEC Pharma 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 HEC-68498’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.

HEC-68498 overview

HEC-68498 is under development for the treatment of idiopathic pulmonary fibrosis and solid tumors including colorectal cancer, breast cancer, human epidermal growth factor receptor 2 negative breast cancer (HER2- breast cancer), triple negative breast cancer and neuroendocrine cancers. The drug candidate is administered through oral route. It acts by targeting phosphatidylinositol 3 Kinase (PI3K) and mechanistic target of rapamycin (mTOR).

HEC Pharma overview

HEC Pharma is a private company, The Company mainly develops, produces, and distributes active pharmaceutical ingredients, insulins, and more. It is headquartered in Dongguan, Guangdong, China.

For a complete picture of HEC-68498’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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.