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OPDIVO (Bristol-Myers Squibb Australia Pty Ltd)
Product name
OPDIVO
Date registered
Evaluation commenced
Decision date
Approval time
136 (255 working days)
Active ingredients
nivolumab
Registration type
EOI
Indication
OPDIVO, in combination with ipilimumab, is now also indicated for the first-line treatment of adult patients with unresectable or metastatic hepatocellular carcinoma.