Nipah [strain Bangladesh] vaccine is under clinical development by Public Health Vaccines and currently in Phase I for Nipah Virus (NiV) Infections. According to GlobalData, Phase I drugs for Nipah Virus (NiV) Infections does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Nipah [strain Bangladesh] vaccine LoA Report. 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.

Nipah [strain Bangladesh] vaccine overview

Vaccine (rVSV-Nipah vaccine) is under development for the prevention of Nipah virus infections. The vaccine candidate is a live, attenuated recombinant vesicular stomatitis virus (rVSV) vector that expresses the glycoprotein (G) of the Nipah virus (Bangladesh strain). It is administered through intramuscular route.

For a complete picture of Nipah [strain Bangladesh] vaccine’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.