NC-525 is under clinical development by NextCure and currently in Phase I for Refractory Acute Myeloid Leukemia. According to GlobalData, Phase I drugs for Refractory Acute Myeloid Leukemia have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how NC-525’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.

NC-525 overview

NC-525 is under development for the treatment of relapsed and refractory acute myelocytic leukemia (AML), myelodysplastic syndrome, chronic myelomonocytic leukemia (CMML). It is administered by intravenous route. It is a monoclonal antibody targeting leukocyte associated immunoglobulin like receptor 1 (LAIR1).

NextCure overview

NextCure is a biopharmaceutical company that develops immune medicines to treat cancer and other immune-related diseases. The company’s product portfolio includes the FIND-IO technology platform to discover and understand targets and structural components of immune cells and their functional impact in order to develop immune medicines. Its pipeline products include protein drugs such as NC762, NC525 and NC410 are expressed on highly immunosuppressive cells and tumor cells. It is also pursuing partnering opportunities with pharmaceutical and biotechnology companies to discover and develop biologic-based therapeutics for the treatment of cancer, autoimmune and neurological disorders and expanding to a variety of therapeutic areas. NextCure is headquartered in Beltsville, Maryland, the US.

For a complete picture of NC-525’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.