LIS-1 is under clinical development by Xenothera and currently in Phase II for Anaplastic Large Cell Lymphoma (ALCL). According to GlobalData, Phase II drugs for Anaplastic Large Cell Lymphoma (ALCL) have a 29% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how LIS-1’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.
LIS-1 overview
LIS-1 (polyclonal antibodies) are under development for kidney transplantation, graft versus host disease, graft rejection following solid organ transplantation, anaplastic large cell lymphoma, peripheral t-cell lymphomas and natural killer cell lymphomas. The drug candidates are polyclonal antibodies developed based on Xenothera technology platform involving generation of hyperimmune polyclonal sera. It is administered through intravenous route.
Xenothera overview
Xenothera, is a xenotherapy platform with embedded technology that renovates immunological treatments. The company is headquartered in France.
For a complete picture of LIS-1’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.
