BRIEF-FDA Approves KEYTRUDA® (pembrolizumab) And KEYTRUDA QLEX™ (Pembrolizumab And Berahyaluronidase Alfa-Pmph), Each With Padcev® (enfortumab vedotin-ejfv)

Reuters

11/22

Nov 21 (Reuters) - Merck & Co Inc MRK.N:

FDA APPROVES KEYTRUDA® (PEMBROLIZUMAB) AND KEYTRUDA QLEX™ (PEMBROLIZUMAB AND BERAHYALURONIDASE ALFA-PMPH), EACH WITH PADCEV® (ENFORTUMAB VEDOTIN-EJFV), AS PERIOPERATIVE TREATMENT FOR ADULTS WITH CISPLATIN-INELIGIBLE MUSCLE-INVASIVE BLADDER CANCER

Source text: ID:nBw46rHP9a

Further company coverage: MRK.N

((Reuters.Briefs@thomsonreuters.com;))

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</span>Merck &amp; Co Inc <span>MRK.N</span>:</p><ul><li><p>FDA APPROVES KEYTRUDA® (PEMBROLIZUMAB) AND KEYTRUDA QLEX™ (PEMBROLIZUMAB AND BERAHYALURONIDASE ALFA-PMPH), EACH WITH PADCEV® (ENFORTUMAB VEDOTIN-EJFV), AS PERIOPERATIVE TREATMENT FOR ADULTS WITH CISPLATIN-INELIGIBLE MUSCLE-INVASIVE BLADDER CANCER</p></li></ul><p>Source text: <span>ID:nBw46rHP9a</span></p><p>Further company coverage: <span>MRK.N</span></p><p> ((Reuters.Briefs@thomsonreuters.com;))</p></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU1917777945.USD","symbol_name":"安联专题基金Cl AT Acc","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251121:nTUA2GCLVB:1","article_id":"2585126036","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2585126036","pubTimestamp":1763761614,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"BRIEF-FDA Approves KEYTRUDA (pembrolizumab) And KEYTRUDA QLEX (Pembrolizumab And Berahyaluronidase Alfa-Pmph), Each With Padcev (enfortumab vedotin-ejfv)Nov 21 (Reuters) - 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