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U S Food and Drug Administration Approves Opdivo® (nivolumab) as Adjuvant Treatment for Eligible Patients with Completely Resected Stage IIB or Stage IIC Melanoma1

U S Food and Drug Administration Approves Opdivo® (nivolumab) as Adjuvant Treatment for Eligible Patients with Completely Resected Stage IIB or Stage IIC Melanoma¹

U S Food and Drug Administration Approves Opdivo® (nivolumab) as Adjuvant Treatment for Eligible Patients with Completely Resected Stage IIB or Stage IIC Melanoma¹
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Bristol-Myers Squibb (BMY) Reports Positive CHMP Opinion Recommending Approval for Opdivo as Adjuvant Treatment

Bristol-Myers Squibb (BMY) Reports Positive CHMP Opinion Recommending Approval for Opdivo as Adjuvant Treatment
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