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KEYTRUDA (Merck Sharp & Dohme (Australia) Pty Ltd)
Product name
KEYTRUDA
Date registered
Evaluation commenced
Decision date
Approval time
243 (255 working days)
Active ingredients
pembrolizumab
Registration type
EOI
Indication
KEYTRUDA (pembrolizumab) is now also indicated as monotherapy for the adjuvant treatment of patients with Stage IB (T2a 4 cm), II, or IIIA NSCLC who have undergone complete resection and platinum-based chemotherapy.