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EMA Validates Application for Frontline Nivolumab Plus Chemo in Advanced Urothelial Cancer
The European Medicines Agency has validated a type II variation application for the first-line combination of nivolumab and cisplatin-based chemotherapy for adult patients with unresectable or metastatic urothelial carcinoma.
Dana walker
Global health status
European union
Bristol myers squibb
European medicines agency
New england journal
Health status
Medicines agency
Bristol myers
Nivolumab and cisplatin based chemotherapy
Patients with unresectable or metastatic urothelial carcinoma
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