Health Canada Approves Merck's Subcutaneous KEYTRUDA for Multiple Cancers

Reuters

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Health Canada has approved KEYTRUDA SC™, a subcutaneous formulation of pembrolizumab from Merck & Co. Inc., for use across multiple cancer indications. The approval is supported by data demonstrating the subcutaneous formulation's noninferiority to the intravenous formulation in patients with metastatic non-small cell lung cancer. The timing for commercial availability will depend on provincial and territorial reimbursement processes.

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: 202602171100CANADANWCANADAPR_C1513) on February 17, 2026, and is solely responsible for the information contained therein.

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Inc., for use across multiple cancer indications. The approval is supported by data demonstrating the subcutaneous formulation's noninferiority to the intravenous formulation in patients with metastatic non-small cell lung cancer. The timing for commercial availability will depend on provincial and territorial reimbursement processes.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>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: 202602171100CANADANWCANADAPR_C1513) on February 17, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU2461242641.AUD","symbol_name":"WELLINGTON US QUALITY GROWTH \"A\" (AUDHDG) ACC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260217:nNDLb7sZfd:1","article_id":"2612146465","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2612146465","pubTimestamp":1771344044,"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":"Health Canada has approved KEYTRUDA SC, a subcutaneous formulation of pembrolizumab from Merck & Co. 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Inc., for use across multiple cancer indications. The approval is supported by data demonstrating the subcutaneous formulation's noninferiority to the intravenous formulation in patients with metastatic non-small cell lung cancer. The timing for commercial availability will depend on provincial and territorial reimbursement processes.\n      \n\n\nDisclaimer: 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. 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