Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NM-IL-12 is a recombinant human interleukin-12 (rHuIL-12) therapy developed as an immunotherapy to enhance antitumor efficacy in cutaneous T-cell lymphoma (CTCL), particularly when combined with low-dose total skin electron beam therapy (TSEBT). Interleukin-12 is a cytokine that stimulates the activity of natural killer (NK) cells and cytotoxic CD8+ T cells, promoting the production of interferon-gamma and shifting immune responses toward a Th1 phenotype. This mechanism aims to improve immune-mediated tumor cell killing while potentially reducing skin-related toxicity associated with radiation. The combination has been evaluated in clinical trials for CTCL, showing promising response rates[1][2][3][4][5].
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 NM-IL-12 + TSEBT.