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Merck

149.86

+2.101.42%

Post-market: 149.85-0.0100-0.01%19:59 EDT

Volume:9.87M

Turnover:1.48B

Market Cap:369.73B

PE:117.74

High:151.68

Open:150.23

Low:148.55

Close:147.76

52wk High:156.92

52wk Low:77.58

Shares:2.47B

Float Shares:2.47B

Volume Ratio:0.98

T/O Rate:0.40%

Dividend:3.32

Dividend Rate:2.22%

EPS(TTM):1.27

EPS(LYR):7.28

ROE:6.96%

ROA:11.87%

PB:8.82

PE(LYR):20.59

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Overview Company News Filings

Movement Alert｜Merck Rises 3.08% in Regular Trading, Keytruda Plus Trodelvy Wins FDA Approval for Triple-Negative Breast Cancer

The Dow Hits Record High, Caterpillar Surges Over 5%

Tiger Newspress

Bio-Techne Surges as Merck Agrees to Acquire Company at $73 Per Share in Cash

Merck Gains FDA Approval for Keytruda Plus Trodelvy in PD-L1 Positive Breast Cancer

MT Newswires Live

Merck says FDA approves Keytruda and Keytruda Qlex in combo with Trodelvy

FDA Approves Keytruda® (pembrolizumab) and Keytruda Qlex™ (pembrolizumab and Berahyaluronidase Alfa-pmph), Each with Trodelvy® (sacituzumab Govitecan-hziy) as First-line Treatment of Pd-l1+ (CPS ≥10) Advanced Triple-negative Breast Cancer (tnbc)

THOMSON REUTERS

Alerts Incorrectly Tagged to Merck & Co Withdrawn

Major Deals Involving US Drugmakers and Biotechs over the Past Decade

Germany's Merck Boosts Life Sciences Business with $11 Billion Bet on Bio-techne

Merck Reviews Regional Distribution Hub Plan In Abu Dhabi

MT Newswires Live

Department of Health Abu Dhabi: Partnership with Msd to Advance Operational Excellence and Expand Access Across Region

THOMSON REUTERS

Merck Initiated at Outperform by CICC

Unicef, Gavi Call to Speed Bundibugyo Ebola Vaccine Access

Merck says EC approves Keytruda plus Padcev combination

EU Approves Merck Keytruda Plus Padcev for Cisplatin-ineligible Resectable Muscle-invasive Bladder Cancer

European Commission Approves Keytruda® (pembrolizumab) Plus Padcev® (enfortumab Vedotin-ejfv) as First Pd-1 Inhibitor Plus Antibody-drug Conjugate Regimen for Adults with Cisplatin-ineligible Resectable Muscle-invasive Bladder Cancer

THOMSON REUTERS

PharmaMar’s Partner Merck Seeks Priority Approval in Japan for Zepzelca as First-Line SCLC Maintenance

CICC Initiates Merck & Co. at Outperform With $138 Price Target

MT Newswires Live

Merck initiated with an Outperform at CICC

Movement Alert｜Merck Rises 3.03% in Regular Trading, Multiple Catalysts Including Phase 3 Trial Success and Potential Major Acquisition

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says FDA approves Keytruda and Keytruda Qlex in combo with Trodelvy","url":"https://stock-news.laohu8.com/highlight/detail?id=2646728168","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2646728168?lang=en_us&edition=fundamental","pubTime":"2026-06-25 18:50","pubTimestamp":1782384637,"startTime":"0","endTime":"0","summary":"Merck (MRK) announced the U.S. FDA approved Keytruda and Keytruda Qlex, each in combination with Trodelvy, Gilead’s (GILD) Trop-2-directed 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