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FDA Approves Libtayo® as Monotherapy for Advanced NSCLC

FDA Approves Libtayo® as Monotherapy for Advanced NSCLC Search jobs Subject: FDA Approves Libtayo     Regeneron and Sanofi received U.S. FDA approval for Libtayo® (cemiplimab-rwlc, an PD-1 inhibitor) for the first-line treatment of patients with advanced non-small cell lung cancer (NSCLC) whose tumors have high PD-L1 expression (tumor proportion score ≥50%), %), as determined by an FDA-approved test. Patients must either have metastatic or locally advanced tumors that are not candidates ...
Naiyer Rizvi Peterc Adamson Georged Yancopoulos Ahmet Sezer Columbia University Irving Medical Center Teva Pharmaceutical Industries Ltd

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