Bempikibart is under clinical development by Q32 Bio Operations and currently in Phase II for Alopecia Areata. According to GlobalData, Phase II drugs for Alopecia Areata have a 48% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Bempikibart’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.

Bempikibart overview

bempikibart (ADX-914) is under development for the treatment of autoimmune, atopic dermatitis, alopecia areata and inflammatory diseases. It acts by targeting interleukin-7 receptor (IL-7R) and thymic stromal lymphopoietin (TSLP). It is a fully human monoclonal antibody. It is administered through subcutaneous route.

Q32 Bio Operations overview

Q32 Bio Operations, formerly Q32 Bio Inc (Q32 Bio), is a biopharmaceutical manufacturing company. It is headquartered in Waltham, Massachusetts, the US.

For a complete picture of Bempikibart’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.