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- W2925717458 abstract "The US Food and Drug Administration (FDA) granted accelerated approval of nivolumab (Opdivo) based on overall response rate (ORR) in classical Hodgkin lymphoma patients." @default.
- W2925717458 created "2019-04-11" @default.
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- W2925717458 date "2016-05-21" @default.
- W2925717458 modified "2023-09-27" @default.
- W2925717458 title "FDA Approves Nivolumab for Relapsed Classical Hodgkin Lymphoma" @default.
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