TIDAL-01 is under clinical development by Turnstone Biologics and currently in Phase I for Triple-Negative Breast Cancer (TNBC). According to GlobalData, Phase I drugs for Triple-Negative Breast Cancer (TNBC) have an 83% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how TIDAL-01’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.

TIDAL-01 overview

TIDAL-01 is under development for the treatment of solid tumors, cutaneous, non-cutaneous melanoma, HER2 negative and HER2 positive breast cancer, triple negative breast cancer, metastatic colorectal cancer and metastatic uveal melanoma. The therapy comprise of tumor-infiltrating lymphocytes (TILs). It is developed based on TIDAL platform. It is administered through parenteral route.

Turnstone Biologics overview

Turnstone Biologics, is a clinical stage biotech company that developing breakthrough cancer immunotherapies. The company is headquartered in Canada.

For a complete picture of TIDAL-01’s drug-specific PTSR and LoA scores, buy the report here.


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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.