FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With Padcev® (enfortumab vedotin-ejfv), as Treatment Before and After Surgery for Ad
Go back to FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With Padcev® (enfortumab vedotin-ejfv), as Treatment Before and After Surgery for Ad| Merck & Co. (NYSE: MRK) | Delayed: 130.42 --0 (-0%) | |||||
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| Previous Close | $130.42 | 52 Week High | $65.46 | |||
| Open | $130.42 | 52 Week Low | $47.97 | |||
| Day High | $130.42 | P/E | 88.72 | |||
| Day Low | $130.42 | EPS | $1.47 | |||
| Volume | 4,988 | |||||

