izuralimab
Term · Oncology and biomedicine · MLC-T-ONC-014612
A humanized, Fc-engineered bispecific monoclonal antibody directed against both the human negative immunoregulatory checkpoint receptor, programmed cell death protein 1 (PD-1; PCD-1; CD279), and inducible T-cell co-stimulator (ICOS; CD278), with potential immunomodulating and antineoplastic activities. Upon administration, izuralimab targets and binds to both PD-1 and ICOS expressed on certain T cells, including tumor-infiltrating lymphocytes (TILs). This prevents the activation of PD-1 by its ligands, programmed cell death-1 ligand 1 (PD-L1) and PD-1 ligand 2 (PD-L2), and stimulates ICOS-mediated signaling, which promotes the activation of T cells and enhances T-cell-mediated immune responses against tumor cells. Combined PD-1 blockade and ICOS stimulation may enhance T-cell activation and proliferation more than targeting each receptor individually. The engineered Fc domain increases the stability and half-life of the antibody.
| Identifier | MLC-T-ONC-014612 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | PD1 x ICOS bispecific monoclonal antibody XmAb23104; anti-PD1/anti-ICOS bispecific monoclonal antibody XmAb23104; anti-PD1/ICOS bispecific monoclonal antibody XmAb23104 |
| References | National Cancer Institute Thesaurus (CC BY 4.0) |
Record as JSON
{
"id": "MLC-T-ONC-014612",
"term": "izuralimab",
"field": "Oncology and biomedicine",
"definition": "A humanized, Fc-engineered bispecific monoclonal antibody directed against both the human negative immunoregulatory checkpoint receptor, programmed cell death protein 1 (PD-1; PCD-1; CD279), and inducible T-cell co-stimulator (ICOS; CD278), with potential immunomodulating and antineoplastic activities. Upon administration, izuralimab targets and binds to both PD-1 and ICOS expressed on certain T cells, including tumor-infiltrating lymphocytes (TILs). This prevents the activation of PD-1 by its ligands, programmed cell death-1 ligand 1 (PD-L1) and PD-1 ligand 2 (PD-L2), and stimulates ICOS-mediated signaling, which promotes the activation of T cells and enhances T-cell-mediated immune responses against tumor cells. Combined PD-1 blockade and ICOS stimulation may enhance T-cell activation and proliferation more than targeting each receptor individually. The engineered Fc domain increases the stability and half-life of the antibody.",
"synonyms": [
"PD1 x ICOS bispecific monoclonal antibody XmAb23104",
"anti-PD1/anti-ICOS bispecific monoclonal antibody XmAb23104",
"anti-PD1/ICOS bispecific monoclonal antibody XmAb23104"
],
"references": [
"National Cancer Institute Thesaurus"
],
"url": "https://mlchart.com/terminology/oncology/izuralimab/"
}
Record 9,669 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.