relatlimab — Drug Monograph
Brand names: Opdualag (with nivolumab)
Drug class: Checkpoint Inhibitor
Mechanism of Action
LAG-3 (Lymphocyte-Activation Gene 3) blocking monoclonal antibody. LAG-3 is an inhibitory co-receptor expressed on exhausted CD4+ and CD8+ T cells, and its engagement by MHC class II molecules (and other ligands) suppresses T-cell proliferation and effector function. Relatlimab blocks LAG-3 signaling, restoring T-cell activity. When combined with nivolumab (PD-1 blockade), dual checkpoint inhibition achieves synergistic reinvigoration of tumor-infiltrating T cells. Relatlimab is only available as a fixed-dose combination with nivolumab (Opdualag: relatlimab 160 mg + nivolumab 480 mg per 20…
FDA Indications
- Unresectable or metastatic melanoma (adults and pediatric patients ≥12 years), as a fixed-dose combination with nivolumab (Opdualag) (FDA approval March 2022, RELATIVITY-047: PFS 10.1 vs 4.6 months, HR 0.75; OS HR 0.80 vs nivolumab monotherapy)
Common Side Effects
- Fatigue
- Musculoskeletal pain
- Rash
- Pruritus
- Diarrhea
- Hypothyroidism
- Nausea
- Decreased appetite
Clinical Pearl
Relatlimab represents the first approved LAG-3 inhibitor in oncology and the first approved dual checkpoint combination targeting two distinct co-inhibitory receptors (LAG-3 + PD-1). RELATIVITY-047 showed ~2-fold improvement in PFS vs nivolumab alone in first-line metastatic melanoma. Importantly, LAG-3 and PD-1 co-expression on tumor-infiltrating lymphocytes (TILs) is a biomarker of T-cell exhaustion; dual blockade is synergistic. The irAE profile resembles nivolumab but with higher rates due…
Related Therapies & Mechanisms
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