Drug intelligence / Profile preview

CC-122 + nivolumab

Development stage
Phase 2
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

CC-122 + nivolumab is an experimental **combination therapy** consisting of CC-122 (avadomide), a novel immunomodulatory small molecule with structural similarity to thalidomide, and nivolumab, a monoclonal antibody immune checkpoint inhibitor targeting programmed cell death protein 1 (PD-1)[2][4][1]. - **CC-122 (avadomide)** acts by binding cereblon (CRBN), leading to ubiquitin-mediated degradation of transcription factors IKZF1 and IKZF3, derepressing interferon (IFN)-regulated genes, promoting apoptosis of malignant cells, and modulating T and B cell activity by costimulation and increased IL-2 production[2]. - **Nivolumab** is a human monoclonal antibody inhibiting PD-1 on T cells, blocking interaction with its ligands (PD-L1/PD-L2), resulting in enhanced immune response against tumor cells[5]. The combination aims to leverage CC-122’s immunomodulatory and antineoplastic effects with nivolumab’s checkpoint inhibition to synergistically activate anti-tumor immunity. Clinical development has included dose escalation studies in unresectable hepatocellular carcinoma (HCC), and advanced melanoma[1][4].

Other names
CC-122 + nivolumab
02

Targets

CRBN (Cereblon)IKZF1 (Ikaros family zinc finger protein 1)IKZF3 (Zinc finger protein Aiolos)PDCD1 (Programmed cell death protein 1 receptor)

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