Brief

On "06/03/2025", the "Medicines and Healthcare products Regulatory Agency (MHRA)" issued an update regarding "Lazertinib approved for use in combination with amivantamab for the treatment of adults with non-small cell lung cancer". The approval is based on a clinical trial where participants who received the combination treatment had a longer period without disease progression. Side effects may include skin problems, decreased appetite, nausea, and fever, but detailed information is available in the Patient Information Leaflet or SmPC on the MHRA website.

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Medicines and Healthcare products Regulatory Agency (MHRA)

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