TAC-001 is under clinical development by Tallac Therapeutics and currently in Phase II for Metastatic Melanoma. According to GlobalData, Phase II drugs for Metastatic Melanoma have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how TAC-001’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.
TAC-001 overview
TAC-001 is under development for the treatment of advanced or metastatic solid tumors, colorectal cancer and metastatic melanoma. The drug candidate comprises of monoclonal antibody conjugated with T-CpG. The drug candidate is being developed based on toll-like receptor agonist antibody conjugate (TRAAC) technology. It acts by targeting cells expressing CD22 and acts as TLR9 agonist. It is administered through intravenous route.
Tallac Therapeutics overview
Tallac Therapeutics is a biopharmaceutical company that offers advance novel immunotherapies for Cancer. The company is headquartered in Burlingame, California, the US.
For a complete picture of TAC-001’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.
