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You are here: Industry Insights > KEYNOTE-522

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FDA casts doubt on clinical meaningfulness of Merck’s Keytruda trial data pharmaceutical-technology
February 09, 2021
The US Food and Drug Administration (FDA) has cast doubt on the results from Merck’s KEYNOTE-522 trial of Keytruda (pembrolizumab) submitted to support its expanded label in treating triple-negative breast cancer (TNBC).

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