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TEVIMBRA (Beigene Aus Pty Ltd)

Product name
TEVIMBRA
Date registered
Evaluation commenced
Decision date
Approval time
220 (255 working days)
Active ingredients
tislelizumab
Registration type
EOI
Indication

TEVIMBRA in combination with platinum and fluoropyrimidine-based chemotherapy, is now also indicated for the first-line treatment of adult patients with HER-2 negative locally advanced unresectable or metastatic gastric or gastro-oesophageal junction (G/GOJ) adenocarcinoma

.