EMA validates application for Opdivo + Yervoy and Opdivo + chemotherapy in recurrent or metastatic ESCC indication

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The European Medicines Agency has validated its Type II Variation Marketing Authorization Applications for both Opdivo (nivolumab) in combination with Yervoy (ipilimumab) and Opdivo in combination with fluoropyrimidine- and platinum-containing chemotherapy as first-line treatments for adult patients with unresectable advanced, recurrent or metastatic esophageal squamous cell carcinoma. 

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