Nemolizumab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized |
| Target | Interleukin-31 receptor A |
| Clinical data | |
| Trade names | Nemluvio |
| Other names | CIM-331, CD14152, nemolizumab-ilto |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a624059 |
| License data |
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| Routes of administration | Subcutaneous injection |
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| Pharmacokinetic data | |
| Metabolism | Proteolytic enzymes |
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Nemolizumab, sold under the brand name Nemluvio, is a humanized monoclonal antibody used for the treatment of prurigo nodularis and atopic dermatitis. It is a monoclonal antibody that blocks the interleukin-31 receptor A. Nemolizumab is humanized IgG2 monoclonal antibody that inhibits interleukin-31 signaling by binding selectively to interleukin-31 receptor alpha. It is an interleukin-31 receptor antagonist. IL-31 is a cytokine involved in pruritus, inflammation, epidermal dysregulation and fibrosis. By inhibiting IL-31-induced responses, nemolizumab prevents the release of proinflammatory cytokines and chemokines.
Nemolizumab was approved for medical use in the United States in August 2024, and in the European Union in February 2025. The US Food and Drug Administration (FDA) considers it to be a first-in-class medication.