Merck & Co (MRK)

149.50
+0.00 (0.00%)
NYSE · Last Trade: Sep 22nd, 9:07 AM EDT
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Detailed Quote

Previous Close149.50
Open-
Bid149.64
Ask149.82
Day's RangeN/A - N/A
52 Week Range77.58 - 156.92
Volume19,628
Market Cap378.44B
PE Ratio (TTM)20.51
EPS (TTM)7.3
Dividend & Yield3.400 (2.27%)
1 Month Average Volume10,221,859

Chart

About Merck & Co (MRK)

Merck & Co is a global healthcare company that specializes in the development, manufacturing, and marketing of pharmaceutical products and vaccines. The company is dedicated to improving health outcomes through innovative research and is known for its focus on areas such as oncology, infectious diseases, and immunology. In addition to its pharmaceutical offerings, Merck actively engages in the discovery of new biologics and therapies, working to address some of the most pressing health challenges worldwide. Through its commitment to scientific excellence and patient care, Merck plays a critical role in advancing public health and enhancing quality of life globally. Read More

News & Press Releases

U.S. FDA Approves Update to the Label for WINREVAIR™ (sotatercept-csrk) to Include Data from the Phase 3 HYPERION Trial Evaluating Adults Recently Diagnosed with Pulmonary Arterial Hypertension (PAH, WHO* Group 1 Pulmonary Hypertension)
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has approved an update to the U.S. product label for WINREVAIR™ (sotatercept-csrk) for injection, 45mg, 60mg, based on the Phase 3 HYPERION trial. WINREVAIR, an activin signaling inhibitor, is FDA-approved for the treatment of adults with pulmonary arterial hypertension (PAH, WHO Group 1 pulmonary hypertension) to improve exercise capacity and WHO functional class (FC), and reduce the risk of clinical worsening events, including hospitalization for PAH, lung transplantation and death. Today’s approval updates the WINREVAIR label to include efficacy and safety data from the HYPERION trial evaluating adults newly diagnosed with PAH (WHO FC II or III, diagnosed within 12 months of study screening) at intermediate to high risk of disease progression, providing insights into the role of WINREVAIR when added to background therapy within the first year of a PAH diagnosis.
By Merck & Co., Inc. · Via Business Wire · September 22, 2026
BioNTech Stock Recently Got Downgraded. But Is Wall Street Underestimating Its Cancer Pipeline?fool.com
Investors buying this biotech stock now will get its pipeline essentially for free.
Via The Motley Fool · September 22, 2026
Meta's Muse Sends the Nasdaq to a Record and Rekindles the AI Tradechartmill.com
Via Chartmill · September 22, 2026
3 Reasons to Sell MRK and 1 Stock to Buy Instead
Over the past six months, Merck has been a great trade, beating the S&P 500 by 13.4%. Its stock price has climbed to $149.98, representing a healthy 29.6% in...
Via StockStory · September 22, 2026
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Via Chartmill · September 21, 2026
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Via Chartmill · September 21, 2026
Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for Subcutaneous Administration for All KEYTRUDA® (pembrolizumab) Indications Approved in Japan
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the Ministry of Health, Labor and Welfare (MHLW) in Japan has approved KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) injection for subcutaneous use for all indications approved in Japan for KEYTRUDA® (pembrolizumab), Merck’s anti-PD-1 therapy. In Japan, KEYJECT®, for subcutaneous injection is the planned trademark for KEYTRUDA QLEX. KEYJECT can be administered in one minute every three weeks or in two minutes every six weeks. Berahyaluronidase alfa is a variant of hyaluronidase developed and manufactured by Alteogen Inc. For a list of select indications for which KEYTRUDA and KEYTRUDA QLEX are approved in the United States, see Selected Indications in the U.S. below.
By Merck & Co., Inc. · Via Business Wire · September 21, 2026
Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as Perioperative Treatment for Adults With Resectable Muscle-Invasive Bladder Cancer (MIBC)
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending approval of KEYTRUDA® (pembrolizumab), Merck’s anti-PD-1 therapy, in combination with Padcev® (enfortumab vedotin-ejfv), as neoadjuvant treatment and then continued after radical cystectomy as adjuvant treatment for adults with resectable muscle-invasive bladder cancer (MIBC). This recommendation, which also includes KEYTRUDA SC® [known as KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) in the U.S.], will now be reviewed by the European Commission (EC) for marketing authorization in the European Union (EU), Iceland, Liechtenstein and Norway. A final decision is expected by the fourth quarter of 2026.
By Merck & Co., Inc. · Via Business Wire · September 18, 2026
Merck Launches Your Hive of Whole Health to Support Whole Person Care for People Living With HIV
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today launched Your Hive of Whole Health, a multi-year educational program that helps people living with HIV build personalized networks of support to address their physical, mental, emotional, and social well-being. Unveiled at the 2026 U.S. Conference on HIV/AIDS (USCHA) in Anaheim, California, Sept. 17-20, 2026, the initiative aims to honor the strides made toward ending the epidemic while emphasizing that future progress depends on a collective focus on whole person health.
By Merck & Co., Inc. · Via Business Wire · September 18, 2026
BioNTech Threw in the Towel on Its Colorectal Cancer Vaccine Trial. Should Investors Be Worried?fool.com
BioNTech's recent pipeline setback is a real cause of concern. But investors shouldn't panic.
Via The Motley Fool · September 18, 2026
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Via Chartmill · September 17, 2026
JEPI and JEPQ Yield Way More Than SCHD, but SCHD Could Produce More Passive Income Over the Long Term. Here's Why.fool.com
Long-term holders of the Schwab U.S. Dividend Equity ETF have seen their yield on cost gradually rise.
Via The Motley Fool · September 17, 2026
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Via Chartmill · September 15, 2026
Merck CEO Sees Pipeline Upside as Launches, Animal Health Drive Transformationmarketbeat.com
Merck & Co., Inc. (NYSE:MRK) Chairman and CEO Rob Davis said the company’s “transformation is underway,” citing progress across product launches, clinical data readouts, business development and its Animal Health segment during a Morgan Stanley discussion. Davis said recent pipeline readouts ha
Via MarketBeat · September 14, 2026
Moderna's COVID Vaccine Was a Historic Success. Could Its Cancer Vaccine Be Even Bigger?fool.com
The biotech is entering a new era.
Via The Motley Fool · September 14, 2026
Blue-Chip Stocks Are Looking Anything But Boring With Dividends and Big 2026 Gainsmarketbeat.com
Coca-Cola, Chevron, and Merck have outperformed the S&P 500 in 2026, each pairing strong share-price gains with growing dividends backed by solid fundamentals.
Via MarketBeat · September 14, 2026
2 Outstanding Dividend Stocks to Buy and Hold for 10 Yearsfool.com
Income seekers can't go wrong with these companies.
Via The Motley Fool · September 12, 2026
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These 5 ETFs Are Built for Bear Markets. History Says Now Is a Fantastic Time to Buy.fool.com
During bear markets and recessions, it's good to be invested in "defensive" stocks and funds that hold up better than average.
Via The Motley Fool · September 10, 2026
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Recent Filing Shows That Rep. Maria Elvira Salazar Bought Over $34K Worth of Merck & Co Stockbenzinga.com
September 9, 2026 records indicate that Representative Maria Elvira Salazar filed a purchase of Merck & Co (NYSE:MRK), valued between $34,006 and $160,000. According to the September filing, the transaction occurred
Via Benzinga · September 10, 2026