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USFDA sends CRL to Merck s sBLA regarding KEYTRUDA
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Merck Receives Complete Response Letter From US FDA for Supplemental Biologics License Application for KEYTRUDA® in High-Risk Early-Stage Triple-Negative Breast Cancer
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Merck (MRK) Receives CRL From US FDA for Supplemental Biologics License Application for KEYTRUDA in High-Risk Early-Stage TNBC
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Form 10-K IDEAYA Biosciences, Inc For: Dec 31
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SHAREHOLDER ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of AbbVie Inc
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