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Merck & Co., Inc. Announces FDA Approves Merck's KEYTRUDA
Merck & Co., Inc. Announces FDA Approves Merck's KEYTRUDA
Merck & Co., Inc. Announces FDA Approves Merck's KEYTRUDA® (Pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients with FIGO 2014 Stage III-IVA Cervical Cancer
Merck & Co., Inc. announced the U.S. Food and Drug Administration has approved KEYTRUDA, Merck?s anti-PD-1 therapy, in combination with chemoradiotherapy for the treatment of patients with FIGO ...
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