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.
GLB-001 overview
GLB-001 is under development for the treatment of relapsed or refractory acute myeloid leukemia (R/R AML) and relapsed or refractory higher risk myelodysplastic syndromes (R/R HR-MDS) and unspecified indication. The therapeutic candidate is a molecular glue degrader and is administered though oral route. It is being developed based target protein degradation (TPD) platform.
GluBio Therapeutics overview
GluBio Therapeutics is dedicated to developing targeted protein degraders for human diseases. GluBio Therapeutics is headquartered in San Diego, California, the US.
For a complete picture of GLB-001’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.