MOR-210 is under clinical development by Human Immunology Biosciences and currently in Phase I for Autoimmune Disorders. According to GlobalData, Phase I drugs for Autoimmune Disorders have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how MOR-210’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.

MOR-210 overview

MOR-210 is under development for the treatment of autoimmune disorders, cancer including relapsed or refractory advanced solid tumors. It is administered parenterally through intravenous route. The drug candidate acts by targeting C5a anaphylatoxin chemotactic receptor 1 (C5AR1).The drug candidate is developed based on HuCALPlatinum technology.

Human Immunology Biosciences overview

Human Immunology Biosciences is a biotechnology company focused on developing therapeutics for immune mediated, allergic and inflammatory diseases. The company is headquartered in San Francisco, California, the US.

For a complete picture of MOR-210’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.