VXX-001 is under clinical development by Viravaxx and currently in Phase II for Hepatitis B. According to GlobalData, Phase II drugs for Hepatitis B have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how VXX-001’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
Smarter leaders trust GlobalData
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.
VXX-001 overview
VXX-001 is under development for the treatment of hepatitis B virus infection. The vaccine candidate is developed based on peptide carrier fusion technology (PCFiT) using a fusion protein component of BM32 vaccine responsible for HBV activity. It acts by targeting sodium-taurocholate cotransporting polypeptide (NTCP). It is administered through subcutaneous route.
Viravaxx overview
Viravaxx is an emerging biopharmaceutical company focusing on the development of innovative antiviral vaccines and immunodiagnostics. The company is headquartered in Vienna, Austria.
For a complete picture of VXX-001’s drug-specific PTSR and LoA scores, buy the report here.
Data Insights
From
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.
