TTX-030 is under clinical development by Trishula 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 TTX-030’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
TTX-030 overview
TTX-030 is under development for the treatment of solid tumors like pancreatic adenocarcinoma and relapsed/refractory lymphoma. The drug candidate is a monoclonal antibody acts by targeting CD39. It is administered through intravenous route.
It was also under development for the treatment of gastric cancer/GEJ carcinomas.
Trishula Therapeutics overview
Trishula Therapeutics is developing antibody drugs for the treatment of cancers. The company is headquartered in South San Francisco, California, the US.
For a complete picture of TTX-030’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.
