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FDA expands approval of Lorbrena as first line treatment of metastatic NSCLC – Pfizer

Written by | 12 Mar 2021

The FDA approved Pfizer Inc.’s supplemental New Drug Application (sNDA) for Lorbrena (lorlatinib), expanding the indication to include first-line treatment of people with anaplastic lymphoma kinase (ALK)-positive non-small… read more.

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