Bristol Myers Squibb’s subcutaneous formulation of its cancer blockbuster Opdivo proved noninferior to intravenous Opdivo in a Phase III trial, the company announced on Thursday.
The study tested subcutaneous Opdivo (nivolumab) in an open-label trial for patients with clear cell renal cell carcinoma (ccRCC), though CMO Samit Hirawat has expressed interest in applying the data “to all other indications where Opdivo is used today as a single agent,” according to an AlphaSense transcript of the company’s first-quarter earnings call.
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