Lyssavirus infections is an indication for drug development with over 60 pipeline drugs currently active. According to GlobalData, preregistered drugs for Lyssavirus infections have a 100% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Lyssavirus infections compared to historical 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.

Lyssavirus infections overview

The infections caused by a group of lyssaviruses are called as Lyssavirus infections, that includes rabies and Australian bat lyssavirus (ABLV). Lyssaviruses are neurotropic, single-stranded ribonucleic acid (RNA) viruses characterized by a bullet-shaped morphology, a tightly coiled nucleocapsid, and five structural proteins. Lyssaviruses can be transmitted through animal saliva and, less commonly, human saliva. They can also be spread when an infected animal bites or scratches a human.

For a complete picture of PTSR and LoA scores for drugs in Lyssavirus infections, 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.