FDA Approves nivolumab for wild-type advanced melanoma

24 Nov 2015 11:02 AM | Lori Aubrey (Administrator)

The U.S. Food and Drug Administration (FDA) approved the programmed cell death protein 1 (PD-1) inhibitor nivolumab (Opdivo) as a single agent for the treatment of patients with BRAF V600 wild-type unresectable or metastatic melanoma.


http://www.ascopost.com/ViewNews.aspx?nid=34078&utm_medium

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Northern New England Clinical Oncology Society
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