T-1101 is under clinical development by Taivex Therapeutics and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 69% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how T-1101’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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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