Drug intelligence / Profile preview

SX-682 + pembrolizumab

Development stage
Unknown
Lead developer
Syntrix Pharmaceuticals
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

SX-682 + pembrolizumab is a combination therapy under clinical investigation for cancer treatment, particularly in metastatic melanoma and non-small cell lung cancer. SX-682 is an oral small-molecule inhibitor of the chemokine receptors CXCR1 and CXCR2, designed to block recruitment of pro-tumoral myeloid-derived suppressor cells (MDSCs) and thereby enhance anti-tumor immunity. Pembrolizumab (Keytruda) is a monoclonal antibody immune checkpoint inhibitor targeting the PD-1 receptor on T cells, thereby activating immune responses against tumor cells. The combination is being studied to determine whether CXCR1/2 inhibition (by SX-682) can improve the clinical efficacy of PD-1 inhibition (by pembrolizumab) by overcoming immunosuppression within the tumor microenvironment[1][3][4][5][6][7].

Other names
SX-682 plus pembrolizumabSX682 plus pembrolizumabSX 682 plus pembrolizumabSX-682 and pembrolizumabSX682 and pembrolizumabSX 682 and pembrolizumabSX-682 + Keytruda
02

Targets

CXCR1 (C-X-C chemokine receptor 1)CXCR2 (C-X-C Motif Chemokine Receptor 2)PDCD1 (Programmed cell death protein 1 receptor)

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