Ketamine is under clinical development by Psycheceutical and currently in Phase I for Post-Traumatic Stress Disorder (PTSD). According to GlobalData, Phase I drugs for Post-Traumatic Stress Disorder (PTSD) 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 Ketamine 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.
Ketamine overview
Ketamine is under development for the treatment of post-traumatic stress disorder (PTSD). It is administered through topical route. The drug candidate acts by targeting N-methyl-D-aspartate (NMDA) receptor and is being developed based on NeuroDirect non-systemic delivery technology.
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For a complete picture of Ketamine’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.
