Drug intelligence / Profile preview

nivolumab + elotuzumab + pomalidomide + dexamethasone

Development stage
Discontinued
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

A quadruplet combination regimen consisting of **nivolumab** (anti-PD-1 monoclonal antibody immune checkpoint inhibitor), **elotuzumab** (anti-SLAMF7 monoclonal antibody activating NK cells and enhancing antibody-dependent cell-mediated cytotoxicity), **pomalidomide** (oral immunomodulatory agent enhancing immune responses and direct cancer cell toxicity), and **dexamethasone** (synthetic glucocorticoid corticosteroid with anti-inflammatory and anti-proliferative effects). This regimen was explored for treatment of **relapsed or refractory multiple myeloma** in clinical trials. The underlying rationale is that pomalidomide can sensitize myeloma cells to immune-mediated attack, dexamethasone supports control of inflammation, elotuzumab enhances NK cell and monoclonal antibody cytotoxicity, while nivolumab augments cytotoxic T cell activity by blocking PD-1 checkpoint signaling, collectively seeking synergistic anti-myeloma effects[1][3][5][7]. Trials indicated modest or no added benefit over standard combinations, and development was terminated.

Other names
nivolumab + elotuzumab + pomalidomide + dexamethasoneNE-Pd
02

Targets

GR (Glucocorticoid receptor)CRBN (Cereblon)SLAMF7 (Signaling lymphocytic activation molecule family member 7)PDCD1 (Programmed cell death protein 1 receptor)

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