APN-401 is under clinical development by InvIOs and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how APN-401’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.

APN-401 overview

APN-401 is under development for the treatment of various solid tumors. It is an autologous cell therapy. The drug candidate is administered through intravenous route and acts by targeting the E3 ubiquitin ligase Cbl-b.

It was under development for the treatment of melanoma, renal carcinoma (kidney), metastatic pancreatic cancer, metastatic colorectal cancer.

InvIOs overview

InvIOs a subsidiary of APEIRON Biologics AG, is a biotech company that focused on the discovery and development of cancer immunotherapies. InvIOs is headquartered in Vienna, Austria.

For a complete picture of APN-401’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.