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.

QEQ-278 overview

QEQ-278 is under development for the treatment of solid tumors including non small cell lung cancer, renal cell carcinoma, esophageal squamous cell carcinoma and human papilloma virus associated head and neck squamous cell carcinoma. It is administered through intravenous route. The drug candidate acts by targeting NKG2DL.

For a complete picture of QEQ-278’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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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.