AMXI-5001 is under clinical development by AtlasMedx and currently in Phase II for Advanced Malignancy. According to GlobalData, Phase II drugs for Advanced Malignancy does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the AMXI-5001 LoA Report. 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.
AMXI-5001 overview
AMXI-5001 is under development for the treatment of advanced malignancies including breast cancer and ovarian cancer. The drug candidate acts by targeting poly ADP-ribose polymerase (PARP) and microtubule polymerization. It is administered through oral route.
For a complete picture of AMXI-5001’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.
