LCTB-21 is under clinical development by Perha Pharmaceuticals and currently in Phase I for Down Syndrome. According to GlobalData, Phase I drugs for Down Syndrome 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 LCTB-21 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.

LCTB-21 overview

LCTB-21 is under development for the treatment of cognitive disorders associated with trisomy 21 (down syndrome) and Alzheimer's disease. It is derived from marine sponge leucettamine B. It targets dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A). It is administered through oral route.

For a complete picture of LCTB-21’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 16 July 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.