BSI-04702 is under clinical development by OBI Pharma and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 38% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how BSI-04702’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
BSI-04702 overview
BSI-04702 (OBI-992) is under development for the treatment of solid tumors, including non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), and gastric cancer (GC). It is administered through parenteral route. The therapeutic candidate comprises of antibody targeting tumor associated calcium signal transducer 2 (Trop 2) with the topoisomerase I (TOP1) payload. It is being developed based on SynTracer HT (high throughput) endocytosis and GlycOBI ADC platform.
OBI Pharma overview
OBI Pharma is a clinical-stage oncology company that develops therapies for the treatment of cancer and infectious diseases. The company’s pipeline products include adagloxad simolenin, an active immunotherapy that is intended for the treatment of metastatic breast cancer. Its other pipelines include OBI-833, OBI-3424, OBI-992, OBI-902, OBI-904 and BsADC fo the indications (NSCLC) non-small cell lung cancer, liver (HCC) hepatocellular carcinoma and T-ALL and solid tumor. The company work in collaboration with research institutes including cancer centers to enhance its pipeline products. The company operates in the US, Taiwan, Hong Kong, Australia and China. OBI Pharma is headquartered in Taipei, Taiwan.
For a complete picture of BSI-04702’s drug-specific PTSR and LoA scores, buy the report here.
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