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: 148.78 +0.80 (0.54%) | |||||
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| Previous Close | $147.98 | 52 Week High | $65.46 | |||
| Open | $148.06 | 52 Week Low | $47.97 | |||
| Day High | $149.98 | P/E | 101.21 | |||
| Day Low | $147.48 | EPS | $1.47 | |||
| Volume | 8,290,254 | |||||
