US FDA approves new Bristol Myers cancer immunotherapy

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WASHINGTON - Bristol Myers Squibb said on Friday that US regulators approved the first medication in a new class of cancer immunotherapies as an initial treatment for advanced melanoma, the deadlies

t form of skin cancer.

The US Food and Drug Administration approved relatlimab from a class known as LAG-3 inhibitors - short for lymphocyte-activation gene 3 - for use in combination with Bristol's blockbuster immunotherapy Opdivo as an initial treatment for advanced melanoma. The medicine is Bristol Myers' third approved cancer immunotherapy - drugs that enlist the body's defences in the fight against tumours. Opdivo targets a protein called PD-1.Relatlimab will only be used in combination with Opdivo, Chief Medical Officer Samit Hirawat said in an interview.

 

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