Risperidone is under clinical development by Valiseek and currently in Phase II for Pancreatic Ductal Adenocarcinoma. According to GlobalData, Phase II drugs for Pancreatic Ductal Adenocarcinoma 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 Risperidone 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.

Risperidone overview

Risperidone (VAL-401) is under development for the treatment of metastatic non-small cell lung adenocarcinoma, pancreatic ductal adenocarcinoma and breast cancer. The drug candidate is formulated as liquid lipid-filled capsule and administered through oral route. The drug candidate acts by targeting hydroxysteroid 17-beta dehydrogenase 10 (HSD17B10) or (HSD10).

It was under development for prostate cancer.

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

This content was updated on 10 June 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.