KYN-5356 is under clinical development by Kynexis Therapeutics and currently in Phase I for Cognitive Impairment Associated With Schizophrenia (CIAS). According to GlobalData, Phase I drugs for Cognitive Impairment Associated With Schizophrenia (CIAS) 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 KYN-5356 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.

KYN-5356 overview

KYN-5356 is under development for the treatment of cognitive impairment associated with schizophrenia (CIAS). The drug candidate is a small molecule which acts by targeting KAT-II.

Kynexis Therapeutics overview

Kynexis Therapeutics, a subsidiary of KyNexis BV, is a biotechnology company engaged in research and development of precision therapeutics for treatment of brain diseases. The company is headquartered in Cambridge, Massachusetts, the US.

For a complete picture of KYN-5356’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 7 February 2024

Premium Insights

From

The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.

GlobalData

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.