ACE-1831 is under clinical development by Acepodia and currently in Phase I for B-Cell Non-Hodgkin Lymphoma. According to GlobalData, Phase I drugs for B-Cell Non-Hodgkin Lymphoma have a 72% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ACE-1831’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
ACE-1831 overview
ACE-1831 is under development for the treatment of CD20-positive B-cell non-Hodgkin's lymphoma. The therapeutic candidate comprises of off-the-shelf NK like gamma delta T cells armed with antibodies and acts by targeting CD 20 expressing hematological tumor cells. It is being developed based on the antibody-cell conjugation (ACC) technology platform. It is administered through intravenous route.
Acepodia overview
Acepodia is a biotechnology company that develops cell therapies to treat cancers. Its pipeline include ACE1831, ACE1708 and ACE2016. ACE1831 is a drug against CD20-indicated hematological cancers; ACE1708 an off-the-shelf NK-like gamma delta T therapy for PD-L1 expressed solid tumors; ACE2016 is an off-the-shelf ?d2 T cell therapy candidate developed from Acepodia’s proprietary ACC platform. Acepodia utilizes its antibody-cell conjugation (ACC) technology platform to develop immunotherapies. The company has operations in New Taipei City, Taiwan. Acepodia is headquartered in New Taipei, Taiwan.
For a complete picture of ACE-1831’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.
