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The European Commission approves the use of Erbitux in head and neck cancer

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THE EUROPEAN COMMISSION,

APPROVES THE USE OF ERBITUX

The European Commission approves the use of Erbitux® in head and neck cancer.

In late November, Merck Serono (the biotech subsidiary of Merck KGaA) received European Commission approval to extend the indication for Erbitux® (the world's first custom-designed monoclonal antibody for inhibiting the proliferation of tumor cells) to the treatment of patients with locally advanced squamous cell carcinoma of the head and the neck. A study published in the New England Journal of Medicine demonstrated the efficacy of Erbitux in combination with platinum-based chemotherapy.


This represents a considerable step forward, since head and neck cancer leads to over 68,000 deaths worldwide each year and has a 40% metastatic relapse rate.

Merck Serono is located in Lyons (in the Rockefeller healthcare district) and Geneva (Switzerland).

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