Merck to Present New HIV Treatment and Prevention Data at European AIDS Conference 2025

Reuters

2025/10/09

Merck to Present New HIV Treatment and Prevention Data at European AIDS Conference 2025

Merck & Co. Inc. announced that it will present new data from its HIV treatment and prevention pipeline at the 20th European AIDS Conference (EACS 2025), scheduled for October 15-18, 2025, in Paris, France. Planned presentations include an oral presentation on weight and body composition at Week 48 from a Phase 3 trial comparing doravirine/islatravir (DOR/ISL) to bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) for adults with virologically suppressed HIV-1 infection. Additional data to be presented include fasting lipids and insulin resistance from two Phase 3 trials, 96-week safety and pharmacokinetics from a Phase 2 trial of once-weekly islatravir/lenacapavir, and Phase 1 safety and pharmacokinetics of the investigational once-monthly PrEP pill MK-8527 in adults with renal impairment. These results will be presented at the upcoming conference.

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 Business Wire (Ref. ID: 20251009184957) on October 09, 2025, and is solely responsible for the information contained therein.

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Inc. announced that it will present new data from its HIV treatment and prevention pipeline at the 20th European AIDS Conference (EACS 2025), scheduled for October 15-18, 2025, in Paris, France. Planned presentations include an oral presentation on weight and body composition at Week 48 from a Phase 3 trial comparing doravirine/islatravir (DOR/ISL) to bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) for adults with virologically suppressed HIV-1 infection. Additional data to be presented include fasting lipids and insulin resistance from two Phase 3 trials, 96-week safety and pharmacokinetics from a Phase 2 trial of once-weekly islatravir/lenacapavir, and Phase 1 safety and pharmacokinetics of the investigational once-monthly PrEP pill MK-8527 in adults with renal impairment. 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ID: 20251009184957) on October 09, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU1934455277.USD","symbol_name":"AB SICAV I LOW VOLATILITY TOTAL RETURN EQUITY PORT \"AD\" (USD) INC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251009:nNDL3m5lMB:1","article_id":"2574156915","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2574156915","pubTimestamp":1760007637,"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":"Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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Inc. announced that it will present new data from its HIV treatment and prevention pipeline at the 20th European AIDS Conference (EACS 2025), scheduled for October 15-18, 2025, in Paris, France. Planned presentations include an oral presentation on weight and body composition at Week 48 from a Phase 3 trial comparing doravirine/islatravir (DOR/ISL) to bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) for adults with virologically suppressed HIV-1 infection. Additional data to be presented include fasting lipids and insulin resistance from two Phase 3 trials, 96-week safety and pharmacokinetics from a Phase 2 trial of once-weekly islatravir/lenacapavir, and Phase 1 safety and pharmacokinetics of the investigational once-monthly PrEP pill MK-8527 in adults with renal impairment. These results will be presented at the upcoming conference.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. 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