FDA grants Priority Review for Keytruda + chemotherapy as first-line for squamous NSCLC

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FDA has accepted for review a supplemental Biologics License Application for Keytruda, Merck’s anti-PD-1 therapy, in combination with carboplatin-paclitaxel or nab-paclitaxel as a first-line treatment for metastatic squamous non-small cell lung cancer, regardless of PD-L1 expression.

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