GXV-001 is under clinical development by GEXVal and currently in Phase I for Fragile X Syndrome. According to GlobalData, Phase I drugs for Fragile X 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 GXV-001 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.

GXV-001 overview

GXV-001 is under development for the treatment of Rett syndrome, fragile X syndrome, Angelman syndrome. The drug candidate act by modulating G protein-coupled receptor (GPCR). It is administered through oral route.

GEXVal overview

GEXVal., is a provider of drug discovery technologies designed to focus on orphan and intractable diseases that help patients and families fighting against orphan and intractable diseases. The company is headquartered in Japan.

For a complete picture of GXV-001’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.