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Merck

78.97

+1.351.74%

Post-market: 79.000.0300+0.04%19:57 EDT

Volume:9.86M

Turnover:778.72M

Market Cap:198.30B

PE:11.48

High:79.49

Open:78.30

Low:78.21

Close:77.62

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Overview Company News Filings

Merck & Co. Inc. Stock Outperforms Competitors On Strong Trading Day

Merck Says First Patient Dosed in Phase 3 Study of Ifinatamab Deruxtecan

MT Newswires Live

Ideate-Esophageal01 Phase 3 Trial of Ifinatamab Deruxtecan Initiated in Certain Patients With Pretreated Advanced or Metastatic Esophageal Squamous Cell Carcinoma

THOMSON REUTERS

Mixed options sentiment in Merck (MRK), with shares up $1.25 (+1.68%) near $76.06

Merck & Co. Inc. to Present New Clinical and Outcomes Research Data on Pulmonary Arterial Hypertension at the American Thoracic Society's International Conference

1 Beaten-Down Stock to Buy Right Now, and 1 to Avoid

Stock Track | Merck Stock Soars 5% as Trump's Drug Pricing Order Sparks Investor Optimism

BRIEF-UK's MHRA Approves Vaccine To Protect Against Pneumococcal Infections Like Pneumonia & Meningitis

UK's Mhra: Approved Capvaxive for People Aged 18 Years & Older to Help Protect Against Pneumococcal Infections

THOMSON REUTERS

UK's Mhra: Approves Vaccine to Protect Against Pneumococcal Infections Such as Pneumonia and Meningitis - Website

THOMSON REUTERS

Immutep Says Efti Triple Combination Improves Response Rate in Non-Small Cell Lung Cancer

MT Newswires Live

BRIEF-Merck Announces Phase 3 Keynote-B96 Trial Met Primary Endpoint Of Progression-Free Survival (Pfs) In Patients With Platinum-Resistant Recurrent Ovarian Cancer Whose Tumors Expressed Pd-L1 And In All Comers

Merck Says Late-Stage Ovarian Cancer Trial for Keytruda Meets Primary Endpoint

MT Newswires Live

Merck Announces Successful Phase 3 Trial Results for KEYTRUDA in Treating Platinum-Resistant Ovarian Cancer

Merck & Co Inc - Study Meets Secondary Endpoint of Overall Survival

THOMSON REUTERS

Merck Announces Phase 3 Keynote-B96 Trial Met Primary Endpoint of Progression-Free Survival (Pfs) in Patients With Platinum-Resistant Recurrent Ovarian Cancer Whose Tumors Expressed Pd-L1 and in All Comers

THOMSON REUTERS

Merck Gets FDA Approval for Tumor Treatment Welireg

Merck Gets FDA Approval for Welireg to Treat Rare Tumors

MT Newswires Live

Merck’s Welireg for PPGL approved by FDA

BRIEF-FDA Approves Merck’S WELIREG® (Belzutifan) For The Treatment Of Adults And Pediatric Patients 12 Years And Older With Locally Advanced, Unresectable, Or Metastatic Pheochromocytoma Or Paraganglioma (PPGL)

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Inc. Stock Outperforms Competitors On Strong Trading Day","url":"https://stock-news.laohu8.com/highlight/detail?id=2536563039","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2536563039?lang=en_us&edition=fundamental","pubTime":"2025-05-20 04:34","pubTimestamp":1747686840,"startTime":"0","endTime":"0","summary":"This article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Merck & Co. Inc.  rose 1.54% to $77.23 Monday, on what proved to be an all-around favorable trading session for the stock market, with the S&P 500 Index  rising 0.09% to 5,963.60 and the Dow Jones Industrial Average  rising 0.32% to 42,792.07.This was the stock's third consecutive day of gains.Merck & Co. Inc. closed 42.64% short of its 52-week high of $134.63, which the company reached on June 25th.The stock outperformed some of its competitors Monday, as Johnson & Johnson  rose 0.77% to $152.49, Pfizer Inc.  rose 0.74% to $23.00, and Eli Lilly & Co.  fell 0.30% to $755.11.Trading volume  remained 5.8 million below its 50-day average volume of 17.5 M.Data source: Dow Jones Market Data, FactSet. Data compiled May 19, 2025.This content was created by MarketWatch, which is operated by Dow Jones & Co. 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options sentiment in Merck (MRK), with shares up $1.25 (+1.68%) near $76.06","url":"https://stock-news.laohu8.com/highlight/detail?id=2536334293","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2536334293?lang=en_us&edition=fundamental","pubTime":"2025-05-17 03:10","pubTimestamp":1747422611,"startTime":"0","endTime":"0","summary":"Options volume is relatively light, with 36k contracts traded and calls leading puts for a put/call ratio of 0.69, compared to a typical level near...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/mixed-options-sentiment-in-merck-mrk-with-shares-up-1-25-1-68-near-76-06?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/mixed-options-sentiment-in-merck-mrk-with-shares-up-1-25-1-68-near-76-06?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["MRK","LU0238689110.USD","LU2106854487.HKD","LU0208291251.USD","SG9999014559.SGD","LU0320765489.SGD","IE00BJT1NW94.SGD","LU0122379950.USD","LU2461242641.AUD","LU2361045086.USD","LU2468319806.SGD","SG9999002232.USD","LU2023250843.SGD","IE0009355771.USD","LU1116320737.USD","LU1035773651.USD","LU0203347892.USD","LU0985320562.USD","LU1162221912.USD","LU0106261372.USD","SG9999001176.SGD","IE0002141913.USD","LU1571399168.USD","SG9999014575.USD","IE00BBT3K403.USD","LU0211331839.USD","BK4533","LU1066053197.SGD","LU1934455277.USD","LU0058720904.USD","LU0320765646.SGD","SG9999014542.SGD","LU1066051225.USD","BK4534","IE00BLSP4239.USD","LU1037948897.HKD","LU1941712264.USD","LU1093756168.USD","SG9999015358.SGD","LU0965509101.SGD","LU0965509010.AUD","LU1917777945.USD","LU1974910355.USD","LU0234572021.USD","LU0965508806.USD","LU1699723380.USD","LU1934455863.HKD","LU1989771016.USD","BK4007","LU1066051811.HKD"],"gpt_icon":0},{"id":"2535398770","title":"Merck & Co. Inc. to Present New Clinical and Outcomes Research Data on Pulmonary Arterial Hypertension at the American Thoracic Society's International Conference","url":"https://stock-news.laohu8.com/highlight/detail?id=2535398770","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535398770?lang=en_us&edition=fundamental","pubTime":"2025-05-16 18:45","pubTimestamp":1747392324,"startTime":"0","endTime":"0","summary":"Merck & Co. Inc. to Present New Clinical and Outcomes Research Data on Pulmonary Arterial Hypertension at the American Thoracic Society's International Conference. Merck & Co. Inc. is set to present new clinical and outcomes research data at the American Thoracic Society's  2025 International Conference in San Francisco from May 16-21. The company will showcase preliminary results from a pooled analysis of clinical trial data on WINREVAIR, focusing on its long-term safety and favorable benefit-risk profile in the treatment of pulmonary arterial hypertension . Additionally, Merck will present an overall survival analysis and other outcomes research related to PAH.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. Merck & Co. Inc. published","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250516:nNDLk1Cr2:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0070302665.USD","BK4588","LU1037948541.HKD","SG9999001176.SGD","BK4516","LU1069347547.HKD","LU0234572021.USD","LU2461242641.AUD","IE00B4R5TH58.HKD","IE000M9KFDE8.USD","LU1037948897.HKD","LU0861579265.USD","LU1057294990.SGD","SG9999002232.USD","LU1934455277.USD","LU0006306889.USD","LU1066051498.USD","LU1934455194.USD","LU0203347892.USD","LU1116320901.HKD","LU1066051811.HKD","IE00BFTCPJ56.SGD","LU2023250504.SGD","IE00BSNM7G36.USD","LU2468319806.SGD","LU0122379950.USD","LU1941712348.USD","LU1066051225.USD","SG9999015341.SGD","LU0238689110.USD","LU0965509101.SGD","LU0266013472.USD","LU1699723380.USD","LU2361044865.SGD","LU0320765646.SGD","LU2324357040.USD","LU2106854487.HKD","IE00BN8TJ469.HKD","LU2089984988.USD","LU0208291251.USD","LU1035773651.USD","LU0106261372.USD","BK4533","LU1974910355.USD","LU0203345920.USD","LU1989771016.USD","MRK","SG9999001440.SGD","IE00BLSP4452.SGD","LU1061106388.HKD"],"gpt_icon":1},{"id":"2535366766","title":"1 Beaten-Down Stock to Buy Right Now, and 1 to Avoid","url":"https://stock-news.laohu8.com/highlight/detail?id=2535366766","media":"Motley Fool","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535366766?lang=en_us&edition=fundamental","pubTime":"2025-05-16 17:30","pubTimestamp":1747387800,"startTime":"0","endTime":"0","summary":"Moderna's clinical progress and deep pipeline of mRNA candidates suggest a promising future.Teladoc continues to lose market share in the competitive telehealth space -- a serious concern.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.fool.com/investing/2025/05/16/1-beaten-down-stock-buy-right-now-and-1-to-avoid/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"fool_stock","symbols":["LU1430594728.SGD","LU0965509101.SGD","LU1974910355.USD","LU2361045086.USD","SG9999002224.SGD","IE00B4R5TH58.HKD","MRK","LU0070302665.USD","LU1069347547.HKD","LU0265550359.USD","LU1983299246.USD","SG9999001440.SGD","SGXZ57979304.SGD","LU0965509010.AUD","LU1934455194.USD","LU1917777945.USD","LU2361044865.SGD","LU0106261372.USD","LU1066053197.SGD","LU1861559042.SGD","BK4585","LU0265550946.USD","LU0289739699.SGD","LU0266013472.USD","LU1162221912.USD","LU2461242641.AUD","BK4588","LU0320765646.SGD","SG9999015341.SGD","LU1699723380.USD","TDOC","BK4533","SG9999001176.USD","LU0320765489.SGD","LU1035773651.USD","LU1861558580.USD","IE00BJT1NW94.SGD","SG9999014575.USD","SG9999014542.SGD","LU1037948897.HKD","BK4504","LU1989772840.SGD","SG9999013999.USD","LU2361044949.HKD","SG9999015358.SGD","LU1066051225.USD","LU2023250843.SGD","LU2112291526.USD","BK4548","LU1093756325.SGD"],"gpt_icon":0},{"id":"1173942275","title":"Stock Track | Merck Stock Soars 5% as Trump's Drug Pricing Order Sparks Investor Optimism","url":"https://stock-news.laohu8.com/highlight/detail?id=1173942275","media":"Stock Track","labels":["movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1173942275?lang=en_us&edition=fundamental","pubTime":"2025-05-16 14:43","pubTimestamp":1747377821,"startTime":"0","endTime":"0","summary":"Shares of Merck  surged 5% in intraday trading on Monday, as investors reacted positively to President Donald Trump's executive order on drug pricing. The pharmaceutical giant's stock reached $79.17, marking its largest percentage increase since March 27, 2024, despite initial concerns about potential negative impacts on the industry.The executive order, signed by Trump on Monday morning, aims to lower prescription drug prices in the United States by implementing a \"most favored nation\" pricing ","market":"nz","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_en","symbols":["MRK"],"gpt_icon":1},{"id":"2535737958","title":"BRIEF-UK's MHRA Approves Vaccine To Protect Against Pneumococcal Infections Like Pneumonia & Meningitis","url":"https://stock-news.laohu8.com/highlight/detail?id=2535737958","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535737958?lang=en_us&edition=fundamental","pubTime":"2025-05-16 00:16","pubTimestamp":1747325809,"startTime":"0","endTime":"0","summary":"BRIEF-UK's MHRA Approves Vaccine To Protect Against Pneumococcal Infections Like Pneumonia & MeningitisMay 15  - UK's MHRA:UK'S MHRA: APPROVES VACCINE TO PROTECT AGAINST PNEUMOCOCCAL INFECTIONS SUCH AS PNEUMONIA AND MENINGITIS - WEBSITEUK'S MHRA: APPROVED CAPVAXIVE FOR PEOPLE AGED 18 YEARS & OLDER TO HELP PROTECT AGAINST PNEUMOCOCCAL INFECTIONSFurther company coverage: MRK.N ","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250515:nFWN3RN3K3:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4516","LU0861579265.USD","LU1116320901.HKD","LU0965509010.AUD","LU1093756168.USD","IE00B4R5TH58.HKD","LU0289739699.SGD","LU1116320737.USD","LU1069347547.HKD","IE00B1BXHZ80.USD","SG9999001176.SGD","LU1162221912.USD","LU0203347892.USD","LU0058720904.USD","IE00BJT1NW94.SGD","LU0238689110.USD","IE000M9KFDE8.USD","LU1291159041.SGD","BK4007","SG9999015341.SGD","LU1093756325.SGD","LU0070302665.USD","LU1934455194.USD","LU1430594728.SGD","LU0234572021.USD","SG9999014567.USD","LU1917777945.USD","LU2089984988.USD","LU0203345920.USD","LU1974910355.USD","LU1941712348.USD","SG9999001440.SGD","SG9999014575.USD","LU1066053197.SGD","LU1929549753.HKD","IE0002141913.USD","BK4588","IE00BLSP4239.USD","MRK","SG9999014559.SGD","LU1934455277.USD","SG9999013999.USD","LU0265550359.USD","SG9999002224.SGD","LU0208291251.USD","LU1057294990.SGD","IE00BFTCPJ56.SGD","IE00B2B36J28.USD","BK4559","LU1066051225.USD"],"gpt_icon":1},{"id":"2535873400","title":"UK's 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Mhra: Approves Vaccine to Protect Against Pneumococcal Infections Such as Pneumonia and Meningitis - Website","url":"https://stock-news.laohu8.com/highlight/detail?id=2535107873","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535107873?lang=en_us&edition=fundamental","pubTime":"2025-05-16 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Says Efti Triple Combination Improves Response Rate in Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2535828216","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535828216?lang=en_us&edition=fundamental","pubTime":"2025-05-15 21:02","pubTimestamp":1747314178,"startTime":"0","endTime":"0","summary":"Immutep  said Thursday its investigational drug eftilagimod alpha, or efti, combined with Merck's  Keytruda and doublet chemotherapy achieved a response rate of 60.8% and disease control rate of 90.2% in patients with advanced or metastatic non-squamous non-small cell lung cancer in an investigator-initiated trial.The company said the 60.8% response rate regardless of PD-L1 expression is a \"substantial improvement\" from the historical control of 48%.Safety continues to be favorable for the triple combination, the company said.Immutep said it expects to present additional data from the trial at a medical conference within the year.Shares of Immutep climbed 9.3% in recent premarket activity Thursday, while Merck shares added 1%.","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["LU0203345920.USD","IE0009355771.USD","LU0320765489.SGD","LU0211331839.USD","LU0965509010.AUD","LU1066053197.SGD","LU2324357040.USD","SG9999001176.USD","LU1989772840.SGD","BK4559","IMMP","LU1069347547.HKD","LU1061106388.HKD","BK4550","LU1066051225.USD","LU2112291526.USD","IE00BBT3K403.USD","LU1037948897.HKD","LU1162221912.USD","IE00BJT1NW94.SGD","LU1035773651.USD","MRK","SG9999014567.USD","LU0320765646.SGD","LU1929549753.HKD","IE00B2B36J28.USD","LU0058720904.USD","SG9999015341.SGD","LU2089984988.USD","LU0861579265.USD","LU1291159041.SGD","LU1057294990.SGD","BK4585","SG9999014542.SGD","LU0265550946.USD","LU1699723380.USD","LU2023250843.SGD","LU0965509101.SGD","LU1934455277.USD","IE00BJJMRZ35.SGD","BK4533","LU1934455194.USD","LU1983299246.USD","IE00BLSP4239.USD","LU2461242641.AUD","IE00BLSP4452.SGD","BK4007","LU0234572021.USD","LU2106854487.HKD","LU1066051498.USD"],"gpt_icon":0},{"id":"2535861841","title":"BRIEF-Merck Announces Phase 3 Keynote-B96 Trial Met Primary Endpoint Of Progression-Free Survival (Pfs) In Patients With Platinum-Resistant Recurrent Ovarian Cancer Whose Tumors Expressed Pd-L1 And In All Comers","url":"https://stock-news.laohu8.com/highlight/detail?id=2535861841","media":"Reuters","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535861841?lang=en_us&edition=fundamental","pubTime":"2025-05-15 19:34","pubTimestamp":1747308867,"startTime":"0","endTime":"0","summary":"BRIEF-Merck Announces Phase 3 Keynote-B96 Trial Met Primary Endpoint Of Progression-Free Survival (Pfs) In Patients With Platinum-Resistant Recurrent Ovarian Cancer Whose Tumors Expressed Pd-L1 And In","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250515:nTUA8FLFBG:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SG9999002224.SGD","MRK","BK4559","LU0265550359.USD","LU1929549753.HKD","LU1989772923.USD","BK4007","LU0006306889.USD","IE00BLSP4452.SGD","LU0234572021.USD","IE00BJJMRZ35.SGD","LU1571399168.USD","LU1585245621.USD","LU0965508806.USD","IE00BFTCPJ56.SGD","LU1093756168.USD","LU2112291526.USD","LU2361044865.SGD","LU0965509010.AUD","LU1917777945.USD","LU0266013472.USD","SG9999014559.SGD","IE00BLSP4239.USD","LU0203345920.USD","LU2023250504.SGD","LU1699723380.USD","LU0965509283.SGD","LU1037948897.HKD","LU1934455863.HKD","SG9999014542.SGD","SG9999014567.USD","LU2023250843.SGD","LU0861579265.USD","LU0211331839.USD","LU0070302665.USD","LU1066053197.SGD","LU0058720904.USD","SG9999001440.SGD","LU1037948541.HKD","SG9999015358.SGD","LU1989772840.SGD","IE0002141913.USD","LU1989771016.USD","SG9999013999.USD","BK4588","LU2361045086.USD","LU1057294990.SGD","BK4516","LU1061106388.HKD","LU1941712348.USD"],"gpt_icon":1},{"id":"2535460768","title":"Merck Says Late-Stage Ovarian Cancer Trial for Keytruda Meets Primary Endpoint","url":"https://stock-news.laohu8.com/highlight/detail?id=2535460768","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535460768?lang=en_us&edition=fundamental","pubTime":"2025-05-15 19:22","pubTimestamp":1747308130,"startTime":"0","endTime":"0","summary":"Merck  said Thursday its late-stage trial evaluating its cancer drug Keytruda in combination with chemotherapy with or without bevacizumab met its primary endpoint of progression-free survival in patients with platinum-resistant recurrent ovarian cancer whose tumors expressed PD-L1 and in all comers.The trial also met a secondary endpoint of overall survival in patients whose tumors express PD-L1, the company said.The trial showed no new safety signals for Keytruda as the safety profile remained consistent with that observed in previously reported studies.Merck said the study is continuing and that the final overall survival results for the entire study population will be evaluated at a future analysis.The company's shares were up about 1% in recent premarket activity on Thursday.","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4559","BK4533","SG9999002232.USD","LU1989771016.USD","IE00B4R5TH58.HKD","LU1066051811.HKD","SG9999014567.USD","LU0320765646.SGD","LU0058720904.USD","LU2461242641.AUD","LU1116320901.HKD","LU0265550359.USD","LU1057294990.SGD","LU1093756325.SGD","IE00BJJMRZ35.SGD","LU1934455863.HKD","SSI","LU1430594728.SGD","LU2361044865.SGD","LU2361044949.HKD","SG9999001440.SGD","SG9999002224.SGD","LU0965509101.SGD","LU1941712264.USD","LU0211331839.USD","SG9999001176.SGD","SGXZ57979304.SGD","LU1934455277.USD","LU1037948541.HKD","LU0006306889.USD","BK4516","LU1585245621.USD","LU1571399168.USD","SG9999001176.USD","BK4588","LU0861579265.USD","IE0009355771.USD","IE00BJT1NW94.SGD","LU1116320737.USD","LU2089984988.USD","MRK","LU1929549753.HKD","IE00BSNM7G36.USD","LU0208291251.USD","LU0238689110.USD","SG9999014542.SGD","LU2361045086.USD","LU1162221912.USD","IE0002141913.USD","IE00BFTCPJ56.SGD"],"gpt_icon":1},{"id":"2535084363","title":"Merck Announces Successful Phase 3 Trial Results for KEYTRUDA in Treating Platinum-Resistant Ovarian Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2535084363","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535084363?lang=en_us&edition=fundamental","pubTime":"2025-05-15 18:45","pubTimestamp":1747305946,"startTime":"0","endTime":"0","summary":"Merck & Co. Inc. announced positive results from its Phase 3 KEYNOTE-B96 trial, evaluating the efficacy of KEYTRUDA  in combination with chemotherapy for treating platinum-resistant recurrent ovarian cancer. The study met its primary endpoint, demonstrating a statistically significant improvement in progression-free survival  for patients with PD-L1-expressing tumors and across all participants. Furthermore, a secondary endpoint of overall survival  was achieved in patients whose tumors express PD-L1. This marks the first time an immune checkpoint inhibitor-based regimen has shown an OS benefit in ovarian cancer. The safety profile of KEYTRUDA was consistent with previous studies, with no new safety signals identified. Results will be shared with regulatory authorities and presented at an upcoming medical meeting.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this A","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250515:nNDL2gYXmY:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1941712264.USD","LU0122379950.USD","LU2361045086.USD","LU2361044949.HKD","LU1093756168.USD","LU0211331839.USD","LU1069347547.HKD","IE000M9KFDE8.USD","IE00BJT1NW94.SGD","LU0289739699.SGD","LU0265550359.USD","LU1061106388.HKD","LU2023250504.SGD","LU1934455194.USD","LU1037948541.HKD","LU2468319806.SGD","SG9999001440.SGD","LU0106261372.USD","LU1585245621.USD","IE00BLSP4452.SGD","LU1037948897.HKD","LU0861579265.USD","SG9999002232.USD","LU1093756325.SGD","BK4007","LU0203345920.USD","LU0070302665.USD","LU0266013472.USD","LU1057294990.SGD","LU1291159041.SGD","IE00B1BXHZ80.USD","LU1934455277.USD","LU1066051225.USD","LU2361044865.SGD","LU2023250843.SGD","IE00B2B36J28.USD","IE0009355771.USD","MRK","SG9999002224.SGD","LU0203347892.USD","IE00BLSP4239.USD","LU0320765646.SGD","LU1934455863.HKD","SG9999001176.USD","LU1989772923.USD","LU1571399168.USD","LU1035773651.USD","LU1917777945.USD","LU2089984988.USD","LU1941712348.USD"],"gpt_icon":1},{"id":"2535848097","title":"Merck & Co Inc - Study Meets Secondary Endpoint of Overall Survival","url":"https://stock-news.laohu8.com/highlight/detail?id=2535848097","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535848097?lang=en_us&edition=fundamental","pubTime":"2025-05-15 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Announces Phase 3 Keynote-B96 Trial Met Primary Endpoint of Progression-Free Survival (Pfs) in Patients With Platinum-Resistant Recurrent Ovarian Cancer Whose Tumors Expressed Pd-L1 and in All Comers","url":"https://stock-news.laohu8.com/highlight/detail?id=2535011848","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535011848?lang=en_us&edition=fundamental","pubTime":"2025-05-15 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Gets FDA Approval for Tumor Treatment Welireg","url":"https://stock-news.laohu8.com/highlight/detail?id=2535088685","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535088685?lang=en_us&edition=fundamental","pubTime":"2025-05-15 05:55","pubTimestamp":1747259700,"startTime":"0","endTime":"0","summary":"Merck has received approval from the Food and Drug Administration for Welireg, its oral inhibitor for patients with certain rare types of neuroendocrine tumors.The company said Wednesday the treatment is for locally advanced unresectable, or metastatic pheochromocytoma or paraganglioma, which are caused by certain genetic syndromes or mutations.The approval makes Welireg the only approved and available treatment in the U.S. for eligible patients with advanced PPGL, the company said.\"For patients with advanced PPGL, there has been a lack of approved systemic treatment options available to help manage their disease,\" said Marjorie Green, senior vice president and head of oncology, global clinical development at Merck Research Laboratories.","market":"other","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"Merck Gets FDA Approval for Tumor Treatment 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Gets FDA Approval for Welireg to Treat Rare Tumors","url":"https://stock-news.laohu8.com/highlight/detail?id=2535488548","media":"MT Newswires Live","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535488548?lang=en_us&edition=fundamental","pubTime":"2025-05-15 05:40","pubTimestamp":1747258857,"startTime":"0","endTime":"0","summary":"Merck (MRK) said late Wednesday the US Food and Drug Administration has approved Welireg to treat patients 12 years and older with locally advanced, unresectable, or metastatic pheochromocytoma or 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Welireg for PPGL approved by FDA","url":"https://stock-news.laohu8.com/highlight/detail?id=2535883220","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535883220?lang=en_us&edition=fundamental","pubTime":"2025-05-15 05:20","pubTimestamp":1747257638,"startTime":"0","endTime":"0","summary":"Merck (MRK) announced the FDA has approved Welireg – belzutifan -, Merck’s oral hypoxia-inducible factor-2 alpha inhibitor, for the treatment of 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Approves Merck’S WELIREG® (Belzutifan) For The Treatment Of Adults And Pediatric Patients 12 Years And Older With Locally Advanced, Unresectable, Or Metastatic Pheochromocytoma Or Paraganglioma (PPGL)","url":"https://stock-news.laohu8.com/highlight/detail?id=2535124883","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2535124883?lang=en_us&edition=fundamental","pubTime":"2025-05-15 05:16","pubTimestamp":1747257404,"startTime":"0","endTime":"0","summary":"BRIEF-FDA Approves Merck’S WELIREG (Belzutifan) For The Treatment Of Adults And Pediatric Patients 12 Years And Older With Locally Advanced, Unresectable, Or Metastatic Pheochromocytoma Or 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