Hemay-020 is under clinical development by Tianjin Hemay Pharmaceutical and currently in the Phase I in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.

According to GlobalData, the latest event to affect Hemay-020’s likelihood of approval (LoA) and phase transition for Solid Tumor took place on 27 Jun 2022, which decreased the likelihood that the drug progresses to the next phase in its clinical pathway.

GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their Hemay-020 Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.

Hemay-020 overview

Hemay-020 is under development for the treatment of advanced solid cancer and advanced or metastatic non-small cell lung cancer. It is administered through the oral route. The drug candidate acts by targeting the epidermal growth factor receptor (EGFR). It is a new chemical entity.

Tianjin Hemay Pharmaceutical overview

Tianjin Hemay Pharmaceutical (Hemay) discovers, develops and commercializes novel drugs to treat tumors and immune diseases. The company is investigating preclinical programs including Hemay102, a cyrotoxic anticancer agent targeting hepatocellular carcinoma (HCC); Hemay022, a tyrosine kinase irreversible inhibitor for the treatment of breast cancer; Hemay020, a tyrosince kinase irreversible inhibitor against non-small cell lung cancer (NSCLC); Hemay007, an immunomodulatory agent for Inflammatory Bowel Disease (IBD); and Hemay005, a PDE4 inhibitor to treat psoriasis. It is also evaluating Hemay805, a cytokine inhibitor for influenza, SARS, swine influenza and avian influenza. Hemay has research and development, operations and industrialization centers in Tianjin, Jiangxi, China; Australia and the US. Hemay is headquartered in Tianjin, China.

Quick View Hemay-020 LOA Data

Report Segments
  • Innovator
Drug Name
  • Hemay-020
Administration Pathway
  • Oral
Therapeutic Areas
  • Oncology
Key Developers
Highest Development Stage
  • Phase I

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.