Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
p50-IMC refers to immature myeloid cells (IMCs) that have been genetically modified or derived from a knockout model to lack the p50 subunit of the NF-κB transcription factor. In the context of glioblastoma (GBM), tumor-associated macrophages (TAMs) typically adopt an immunosuppressive M2 phenotype that promotes tumor growth. Research conducted at Virginia Tech and Johns Hopkins University demonstrates that p50-deficient IMCs are biased toward a pro-inflammatory M1 phenotype, characterized by increased expression of TNFα and IL-12b, even under M2-polarizing conditions. When adoptively transferred into orthotopic mouse models of glioblastoma, these cells localize to the tumor and transiently impair tumor growth by shifting the immune microenvironment toward a more active anti-tumor response.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on p50-IMC.