MedPath

Relatlimab

Generic Name
Relatlimab
Brand Names
Opdualag
Drug Type
Biotech
Chemical Formula
-
CAS Number
1673516-98-7
Unique Ingredient Identifier
AF75XOF6W3
Background

Relatlimab is a human IgG4 monoclonal antibody and novel immune checkpoint inhibitor that targets lymphocyte activation gene-3 (LAG-3). It was the first commercially developed anti-LAG-3 antibody, entering clinical trials in 2013, and has garnered interest in the treatment of a variety of cancers, including leukemia and melanoma. As immune checkpoint inhibitors have limited efficacy when used alone, drugs like relatlimab have been trialed in combination with other checkpoint inhibitors - for example, PD-1 inhibitors like nivolumab or CTLA-4 inhibitors like ipilimumab - to enhance their efficacy.

Relatlimab received FDA approval in March 2022, alongside the PD-1 inhibitor nivolumab in the combination product Opdualag (Bristol-Myers Squibb), for the treatment of unresectable or metastatic melanoma. It was the first anti-LAG-3 antibody demonstrate benefit in a Phase 3 study, as well as the first to receive FDA approval.

Indication

Relatlimab is indicated in combination with nivolumab, in the combination product Opdualag, for the treatment of adult and pediatric patients ≥12 years old with unresectable or metastatic melanoma.

Associated Conditions
Metastatic Melanoma, Unresectable Melanoma
Associated Therapies
-
cancernetwork.com
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Clinical Benefit Improves With Relatlimab Combo in Recurrent NSCLC

The RELATIVITY-104 phase 2 study showed improved clinical benefit from adding LAG3 inhibition to anti-PD-1 plus chemotherapy in metastatic non-small cell lung cancer patients with PD-L1 ≥1% and non-squamous histology. Safety was comparable, with no increase in adverse events. Efficacy was assessed with a median PFS of 6.7 months vs 6.0 months, and a 51.3% vs 43.7% overall response rate. These findings support further investigation in a phase 3 study.
targetedonc.com
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Enhanced Outcomes with Relatlimab, Nivolumab, and Chemotherapy in Advanced Non

RELATIVITY-104 study showed improved clinical benefit with relatlimab plus nivolumab and chemotherapy vs nivolumab plus chemotherapy in PD-L1-positive, nonsquamous NSCLC patients, with enhanced PFS and response rates. Safety profiles were comparable, supporting further investigation in phase 3 studies.
onclive.com
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Relatlimab Plus Nivolumab and Chemo Improves Clinical Benefit in Stage IV NSCLC

RELATIVITY-104 study shows Opdualag (relatlimab + nivolumab) plus platinum-doublet chemotherapy improves clinical benefit over nivolumab plus chemotherapy in stage IV or recurrent NSCLC, particularly in PD-L1 ≥1% and nonsquamous histology patients. Safety profiles are comparable, with no increased adverse effects. Efficacy improvements include PFS and ORR, supporting further phase 3 investigation.
statnews.com
·

BMS immunotherapy hits in lung cancer, advancing to Phase 3

Bristol Myers Squibb's Phase 2 RELATIVITY-104 trial showed improved responses in certain lung cancer patients when adding a second immunotherapy to existing checkpoint inhibitor and chemotherapy, leading to a Phase 3 study.
docwirenews.com
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Study Reports 2-Year Survival Data on Nivolumab Plus Relatlimab in NSCLC

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theglobeandmail.com
·

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Investing in dividend-paying stocks like Bristol Myers Squibb and Royalty Pharma can provide steady income, with both companies rapidly increasing their payouts. Bristol Myers Squibb, with a 4.9% yield, has raised its dividend for 15 consecutive years and has multiple growth drivers. Royalty Pharma, offering a 2.9% yield, has seen a 60% increase in free cash flow since 2020 and is poised for exponential growth in royalties and dividends.
biopharmadive.com
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J&J's new cancer drug leads a growing pipeline of dual-targeting treatments

The FDA approved Johnson & Johnson's Rybrevant, a bispecific antibody for treating a specific mutation in non-small cell lung cancer. Bispecific antibodies, targeting two proteins simultaneously, are emerging as a promising treatment for various cancers, including lymphoma, leukemia, and multiple myeloma, with several drugs in advanced clinical trials.
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