Trabedersen is under clinical development by Sapu Bioscience and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Trabedersen’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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, 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 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.
