Health Canada Approves Merck's KEYTRUDA® in Combination with Chemoradiotherapy for Advanced Cervical Cancer

Reuters

07-21

Health Canada Approves Merck's KEYTRUDA® in Combination with Chemoradiotherapy for Advanced Cervical Cancer

Merck & Co. Inc., known as MSD outside of the United States and Canada, has announced that Health Canada has approved KEYTRUDA® (pembrolizumab) for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer in combination with chemoradiotherapy $(CRT)$. This approval is based on the positive results from the Phase 3 KEYNOTE-A18/ENGOT-cx11/GOG-3047 trial, which demonstrated significant improvements in progression-free survival and overall survival for patients receiving the treatment compared to those receiving a placebo. This marks the first approval in Canada for KEYTRUDA® in combination with CRT, providing a vital new therapeutic option for patients battling this stage of cervical cancer.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck & Co. Inc. published the original content used to generate this news brief via CNW (Ref. ID: C3580) on July 21, 2025, and is solely responsible for the information contained therein.

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While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck &amp; Co. Inc. published the original content used to generate this news brief via CNW (Ref. 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Inc., known as MSD outside of the United States and Canada, has announced that Health Canada has approved KEYTRUDA® (pembrolizumab) for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer in combination with chemoradiotherapy <a href=\"https://laohu8.com/S/CRT\">$(CRT)$</a>. This approval is based on the positive results from the Phase 3 KEYNOTE-A18/ENGOT-cx11/GOG-3047 trial, which demonstrated significant improvements in progression-free survival and overall survival for patients receiving the treatment compared to those receiving a placebo. This marks the first approval in Canada for KEYTRUDA® in combination with CRT, providing a vital new therapeutic option for patients battling this stage of cervical cancer.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck &amp; Co. Inc. published the original content used to generate this news brief via CNW (Ref. ID: C3580) on July 21, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU1291159041.SGD","symbol_name":"CPR Invest - Global Silver Age A2 Acc SGD-H","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250721:nNDL4lnClB:1","article_id":"2553408968","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2553408968","pubTimestamp":1753110029,"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":"Merck & Co. Inc., known as MSD outside of the United States and Canada, has announced that Health Canada has approved KEYTRUDA  for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer in combination with chemoradiotherapy . This approval is based on the positive results from the Phase 3 KEYNOTE-A18/ENGOT-cx11/GOG-3047 trial, which demonstrated significant improvements in progression-free survival and overall survival for patients receiving the treatment compared to those receiving a placebo. This marks the first approval in Canada for KEYTRUDA in combination with CRT, providing a vital new therapeutic option for patients battling this stage of cervical cancer.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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Inc., known as MSD outside of the United States and Canada, has announced that Health Canada has approved KEYTRUDA® (pembrolizumab) for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer in combination with chemoradiotherapy $(CRT)$. This approval is based on the positive results from the Phase 3 KEYNOTE-A18/ENGOT-cx11/GOG-3047 trial, which demonstrated significant improvements in progression-free survival and overall survival for patients receiving the treatment compared to those receiving a placebo. This marks the first approval in Canada for KEYTRUDA® in combination with CRT, providing a vital new therapeutic option for patients battling this stage of cervical cancer.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. 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