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Merck Serono, a division of Merck KGaA, announced today that it has received approval from the European Commission to extend the use of its targeted therapy Erbitux® (cetuximab) to include 1st-line treatment of patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck (SCCHN).
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Merck Serono: European Commission Approves Erbitux for 1st-Line Use in ... - PharmiWeb
Erbitux approved for 1st-line use in combination with platinum-based chemotherapy in patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck in Europe Approval based on the results of the EXTREME study, which showed ...
European Commission Approves Erbitux for First-Line Use in Head and ... - Phramalive.com
Approval based on the results of the EXTREME study, which showed first significant overall survival benefit in this setting in 30 years DARMSTADT, Germany, December 1, 2008 ? Merck KGaA and its Merck Serono division announced today that it has ...
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