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.

TACH-101 overview

TACH-101 (formerly QC8222) is under development for the treatment of solid tumors including advanced or metastatic cancer, metastatic colorectal cancer (CRC), esophageal cancer, gastric cancer, breast cancer, triple-negative breast cancer and Diffuse large B-cell lymphomas including germinal-center B-cell-like (GCB), activated B-cell-like (ABC) and primary mediastinal B-cell lymphoma (PMBL). It is administered through oral route. The drug candidate acts as pan-KDM4 epigenetic regulator.

Tachyon Therapeutics overview

Tachyon Therapeutics is a biotechnology company involved in therapeutics for the treatment of advanced cancers. Tachyon Therapeutics is headquartered in Houston, Texas, the US.

For a complete picture of TACH-101’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.