TVAX-006 is under clinical development by Nanjing Yuandasai Weixin Biomedical and currently in Phase I for Herpes Zoster (Shingles). According to GlobalData, Phase I drugs for Herpes Zoster (Shingles) have an 88% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how TVAX-006’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.
TVAX-006 overview
TVAX-006 is under development for the prevention of shingles. The vaccine candidate comprises of varicella-zoster virus glycoprotein E (VZV-gE) antigen and is administered through intramuscular route.
Nanjing Yuandasai Weixin Biomedical overview
Nanjing Yuandasai Weixin Biomedical (Yuandasai Weixin Biomedical) operate in healthcare sector. Yuandasai Weixin Biomedical is headquartered in Nanjing, Jiangsu, China.
For a complete picture of TVAX-006’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.
