Keytruda could be approved for head and neck cancer by June

12 February 2019

Leading immuno-oncology therapy Keytruda (pembrolizumab) will be reviewed for approval in head and neck cancer under the US regulator’s Priority Review scheme.

New Jersey, USA-based Merck & Co (NYSE: MRK) announced its application to broaden the label for the checkpoint inhibitor was accepted by the US Food and Drug Administration, based on data from the KEYNOTE-048 trial.

The trial has been testing the Keytruda-chemo combo as a first-line treatment against recurrent or metastatic head and neck squamous cell carcinoma (HNSCC).

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