DOC-1021 is under clinical development by Diakonos Oncology and currently in Phase I for Pancreatic Ductal Adenocarcinoma. According to GlobalData, Phase I drugs for Pancreatic Ductal Adenocarcinoma does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the DOC-1021 LoA Report. 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.

DOC-1021 overview

DOC-1021 is under development for the treatment of glioblastoma multiforme, pancreatic ductal adenocarcinoma, cutaneous angiosarcoma, prostate cancer and triple negative breast cancer. The therapeutic candidate comprises of dendritic cells.

Diakonos Oncology overview

Diakonos Oncology is a clinical-stage biotechnology company focused on addressing the critical and unmet medical needs of late-stage and aggressive cancers. The company is headquartered in Dallas, Texas, the US.

For a complete picture of DOC-1021’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.