Novartis AG and Chinese partner BeiGene, Ltd. are opting to focus on a combination approach for their PD-1 checkpoint inhibitor tislelizumab in non-small cell lung cancer (NSCLC) in the US, after scrapping a plan to file a biologics license application with the US Food and Drug Administration.
On 19 July, Novartis disclosed in its second-quarter report that it had decided not to move forward with the original plan to submit a BLA in the second half of...
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