T-1101 is under clinical development by Taivex Therapeutics and currently in Phase I for Advanced Malignancy. According to GlobalData, Phase I drugs for Advanced Malignancy 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 T-1101 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.
T-1101 overview
T-1101 is under development for the treatment of advanced malignancies, refractory solid tumors. The drug candidate is a new chemical entity (NCE) administered through oral route. It acts by targeting serine/threonine-protein kinase (Nek2)/highly expressed in cancer (Hec1) mitotic pathway.
Taivex Therapeutics overview
Taivex Therapeutics, is a proprietary technology platform that required for appropriate mitotic progression and chromosomal segregation. The company is headquartered in Taipei, Taiwan.
For a complete picture of T-1101’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.
