BB-1705 is under clinical development by Bliss Biopharmaceutical (Hangzhou) and currently in Phase I for Non-Small Cell Lung Cancer. According to GlobalData, Phase I drugs for Non-Small Cell Lung Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BB-1705’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.
BB-1705 overview
BB-1705 is under development for solid tumor, triple-negative breast cancer, head and neck cancer, non-small cell lung cancer (NSCLC), gastric cancer and unspecified cancer. The drug candidate is a Eribulin-ADC. It acts by targeting epidermal growth factor receptor (EGFR) and is administered through intravenous route of administration.
Bliss Biopharmaceutical (Hangzhou) overview
Bliss Biopharmaceutical (Hangzhou) is a biopharmaceutical company engaged in research, discovery, development and commercialization of anti-tumor macromolecular biotherapeutics and novel drugs for the treatment of various cancer diseases. The company is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of BB-1705’s drug-specific PTSR and LoA scores, buy the report here.
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