BEBT-209 is under clinical development by Guangzhou BeBetter Medicine Technology and currently in Phase I for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer). According to GlobalData, Phase I drugs for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer) have a 90% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BEBT-209’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.
BEBT-209 overview
BEBT-209 is under development for the treatment of HER-2 negative breast cancer, triple-negative breast cancer and brain cancer. The drug candidate acts by targeting cyclin-dependent kinase 4 (CDK4) and cyclin-dependent kinase 6 (CDK6). It is administered through oral route.
Guangzhou BeBetter Medicine Technology overview
Guangzhou BeBetter Medicine Technology (Guangzhou BeBetter Medicine Technology Co) that involves in developing oral biologics to treat autoimmune, inflammatory and metabolic diseases. The company is headquartered in Changsha, China.
For a complete picture of BEBT-209’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.
