Trabedersen is under clinical development by Sapu Bioscience and currently in Phase III for Pancreatic Ductal Adenocarcinoma. According to GlobalData, Phase III drugs for Pancreatic Ductal Adenocarcinoma does not have sufficient historical data to build an indication benchmark PTSR for Phase III. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Trabedersen 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.

Trabedersen overview

Trabedersen (OT-101) is under development for the treatment of pancreatic adenocarcinoma, myelodysplastic syndrome (MDS), long covid-19, malignant melanoma, high grade glioma, colorectal carcinoma, low-grade gliomas and solid tumor in combination with immunotherapy (NK/IL-2),  malignant pleural mesothelioma  and pediatric diffuse intrinsic pontine glioma. The drug candidate is administered by intravenous, infusion and intratumoral route as a solution. It is a single-stranded phosphorothioate antisense oligodeoxynucleotide (18-mer). It is also under development for pneumonia and coronavirus disease 2019 (COVID-19). It was also under development for lung cancer, renal cell cancer, prostate cancer, refractory anaplastic astrocytoma (AA) and other neoplasms, non-small cell lung cancer, glioblastoma.

Sapu Bioscience overview

Sapu Bioscience is an immuno-oncology company that develops RNA therapeutics and small molecule drugs against cancer and infectious diseases. The company is headquartered in San Diego, California, the US.

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

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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.