Hemay-007 is under clinical development by Tianjin Hemay Pharmaceutical and currently in Phase II for Ulcerative Colitis. According to GlobalData, Phase II drugs for Ulcerative Colitis have a 44% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Hemay-007’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
Hemay-007 overview
Hemay-007 is under development for the treatment of inflammatory bowel disease including ulcerative colitis and moderate to severe active rheumatoid arthritis. The drug candidate is formulated as a tablet and administered through the oral route. 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.
For a complete picture of Hemay-007’s drug-specific PTSR and LoA scores, buy the report here.
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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.
