Merck & Co.

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Merck’s investigational pneumonia vaccine, V114, hit the mark in two Phase III studies, including one involving adult HIV patients.
Wrapping up June and ahead of the July 4 holiday, the U.S. Food and Drug Administration (FDA) has a busy two-week period coming up for drug approvals. Here’s a look.
FDA
This is the second such biomarker-specific approval for Keytruda. The first biomarker-specific approval came in 2017.
It was a fairly busy week with clinical trial updates and announcements. Here’s a look.
Please check out the biopharma industry coronavirus (COVID-19) stories that are trending for June 12, 2020.
KEYNOTE-361 is evaluating Keytruda alone and in combination with chemotherapy compared to chemotherapy alone, the current standard of care, for first-line treatment of advanced or metastatic urothelial carcinoma.
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