ATL-001 is under clinical development by Achilles Therapeutics and currently in Phase II for Non-Small Cell Lung Cancer. According to GlobalData, Phase II drugs for Non-Small Cell Lung Cancer have a 39% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how ATL-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.

ATL-001 overview

ATL-001 is under development for the treatment of advanced non-small cell lung cancer and metastatic or recurrent melanoma, head and neck squamous cell carcinoma. The therapeutic candidate comprises of clonal neoantigen T cells (cNeT) isolated from patients own tumor infiltrating lymphocytes (TILs). It is administered through intravenous route.

It was also under development for the treatment of renal cell carcinoma.

Achilles Therapeutics overview

Achilles Therapeutics is a biopharmaceutical company focused on developing personalized T-cell therapies targeting neoantigens present on the surface of cancer cells. It’s lead indications for advanced non-small cell lung cancer and recurrent metastatic melanoma. Achilles uses its proprietary PELEUS bioinformatics platform to identify clonal neoantigens specific to that patient and enable the development of personalized cell therapies targeting cancer cells, without harming healthy tissues. It also operates in Stevenage, Hertfordshire, the UK. Achilles Therapeutics is headquartered in London, Greater London, UK.

For a complete picture of ATL-001’s drug-specific PTSR and LoA scores, buy the report here.

GlobalData

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.