PNA-5 is under clinical development by ProNeurogen and currently in Phase II for Traumatic Brain Injury. According to GlobalData, Phase II drugs for Traumatic Brain Injury does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the PNA-5 LoA Report. 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.

PNA-5 overview

PNA-5 is under development for the treatment of vascular cognitive impairment and dementia (VCID), Alzheimer’s disease related dementias, chronic bone cancer pain, HIV neuropathic pain, inflammatory pain, mild cognitive impairment (PD-MCI) associated Parkinson's disease and traumatic brain injury. It is administered through subcutaneous route. It is a glycosylated Ang-(1-7) peptide acts by targeting MAS receptor. 

For a complete picture of PNA-5’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.