Merck's Phase 3 KEYNOTE-811 Trial Of Keytruda Met Dual Primary Endpoint of Overall Survival as First-Line Treatment Of HER2-Positive Advanced Gastric or Gastroesophageal Junction Adenocarcinoma
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Merck announced that its Phase 3 KEYNOTE-811 trial of Keytruda met its dual primary endpoint of overall survival as a first-line treatment of HER2-positive advanced gastric or gastroesophageal junction adenocarcinoma. This marks a significant advancement in the treatment of this cancer type.
May 01, 2024 | 11:17 am
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Merck's successful Phase 3 trial of Keytruda for advanced gastric cancer could lead to increased sales and potentially further regulatory approvals, positively impacting its stock.
The successful outcome of the KEYNOTE-811 trial demonstrates Keytruda's efficacy in a new indication, which could lead to increased sales and further regulatory approvals. This is likely to be viewed positively by investors, potentially leading to a short-term uptick in Merck's stock price.
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