TORL-3600 is under clinical development by TORL Biotherapeutics 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 TORL-3600’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.
TORL-3600 overview
TORL-3600 is under development for the treatment of advanced solid tumor, colorectal cancer, gastric cancer and pancreatic cancer. The therapeutic candidate is an antibody drug conjugate. It acts by targeting cadherin 17 (CDH17).
TORL Biotherapeutics overview
TORL Biotherapeutics a clinical-stage biopharmaceutical company which operates in healthcare sector and to improve the lives of cancer patients. TORL Biotherapeutics is headquartered in Pasadena, California, the US.
For a complete picture of TORL-3600’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.
