Merck & Co., Inc. (ETR:6MK)
| Market Cap | 321.13B +89.7% |
| Revenue (ttm) | 58.27B +4.6% |
| Net Income | 2.78B -80.7% |
| EPS | 1.11 -80.4% |
| Shares Out | n/a |
| PE Ratio | 115.63 |
| Forward PE | 16.93 |
| Dividend | 2.94 (2.26%) |
| Ex-Dividend Date | Sep 15, 2026 |
| Volume | 373 |
| Open | 130.14 |
| Previous Close | 130.94 |
| Day's Range | 129.52 - 130.50 |
| 52-Week Range | 66.40 - 134.48 |
| Beta | 0.23 |
| Analysts | n/a |
| Price Target | n/a |
| Earnings Date | Oct 29, 2026 |
About Merck & Co.
Merck & Co., Inc. operates as a healthcare company worldwide. It offers human health pharmaceutical for various areas under the Keytruda, Keytruda Qlex, Welireg, Gardasil, ProQuad, M-M-R II, Varivax, Vaxneuvance, Capvaxive, RotaTeq, Pneumovax 23, Bridion, Prevymis, Dificid, Zerbaxa, Winrevair, Adempas/ Verquvo, Ohtuvayre, Lagevrio, Isentress/Isentress HD, Delstrigo, Pifeltro, Belsomra, Januvia, and Janumet brands. The company also provides veterinary pharmaceuticals, vaccines and health management solutions and services, such as livestock produ... [Read more]
Financial Performance
In 2025, Merck & Co.'s revenue was $65.01 billion, an increase of 1.31% compared to the previous year's $64.17 billion. Earnings were $18.25 billion, an increase of 6.64%.
Financial numbers in USD Financial StatementsNews
Merck, Daiichi Sankyo voluntarily withdraw BLA for ifinatamab deruxtecan
The Biologics License Application, or BLA, seeking accelerated approval in the U.S. for Daiichi Sankyo and Merck’s (MRK) ifinatamab deruxtecan for the treatment of adult patients with extensive-stage ...
Merck, Eisai announce FDA approval of Welireg plus Lenvima
Merck (MRK) and Eisai (ESAIY) announced the U.S. FDA has approved the dual oral regimen of Welireg, Merck’s first-in-class oral hypoxia-inducible factor-2 alpha inhibitor, plus Lenvima, the orally ava...
U.S. FDA Approves WELIREG® (belzutifan) Plus LENVIMA® (lenvatinib) for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Component (ccRCC)
RAHWAY, N.J. & NUTLEY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--FDA Approves WELIREG Plus LENVIMA for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Compone...
FDA approves Welireg and Lenvima combo for ccRCC
The Food and Drug Administration approved Welireg from Merck (MRK) in combination with Lenvima from Eisai (ESAIY) for adults with advanced renal cell carcinoma with a clear cell component, or…
Merck's eye disease drug meets main goal in trial
Merck said on Thursday its drug met the main goal in a mid- to late-stage trial testing it in adult patients with a type of disease that affects blood vessels at the back of the eye.
Merck’s remigromig meets primary endpoint in Phase 2b/3 DME trial
Merck (MRK) announced topline results from the pivotal Phase 2b/3 BRUNELLO trial in adults with diabetic macular edema, or DME. BRUNELLO is the first of two Phase 2b/3 trials evaluating…
Merck's Remigromig, a Tri-specific Agonist of the Wingless-related Integration Site (Wnt) Pathway, Met Primary Endpoint in the Pivotal Phase 2b/3 BRUNELLO Study of Adults with Diabetic Macular Edema
RAHWAY, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced topline results from the pivotal Phase 2b/3 BRUNELLO trial in adults with diabet...
Merck says FDA approves update for U.S. product label for Winrevair
Merck (MRK) announced the U.S. FDA has approved an update to the U.S. product label for Winrevair for injection, 45mg, 60mg, based on the Phase 3 HYPERION trial. Winrevair, an…
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)
RAHWAY, N.J.--(BUSINESS WIRE)--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. p...
Pharmaceutical Companies Push Trump Administration to Protect China Deals
A surge in U.S.-China transactions is drawing scrutiny in Washington, where some lawmakers are pushing to slow the pace of investment.
Merck says Japan’s MHLW approves Keytruda Qlex
Merck (MRK) announced the Ministry of Health, Labor and Welfare in Japan has approved Keytruda Qlex injection for subcutaneous use for all indications approved in Japan for Keytruda, Merck’s anti-PD-1...
Merck's KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for Subcutaneous Administration for All KEYTRUDA® (pembrolizumab) Indications Approved in Japan
RAHWAY, N.J.--(BUSINESS WIRE)--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 ...
Merck says CHMP adopts positive opinion on Keytruda/Padcev combination
Merck (MRK) announced the European Medicines Agency’s Committee for Medicinal Products for Human Use adopted a positive opinion recommending approval of Keytruda, Merck’s anti-PD-1 therapy, in combina...
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)
RAHWAY, N.J.--(BUSINESS WIRE)--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 (...
Moderna's AI-Built Cancer Vaccine Clears Phase 3 With Merck
Moderna built an artificial intelligence that reads a patient's tumor and decides what that patient's medicine should be. That approach just cleared its biggest test.
Merck & Co. Transcript: Morgan Stanley 24th Annual Global Healthcare Conference
Transformation is progressing with strong product launches, positive clinical data, and business development driving growth. Pipeline assets like INT and sac-TMT offer significant upside, while LIPFENDRA is positioned for broad access. AI and global innovation are enhancing R&D efficiency.
Perspective Therapeutics announces trial collaboration agreement with Merck
Perspective Therapeutics (CATX) announced a clinical trial collaboration agreement with Merck (MRK). The agreement supports the evaluation of Perspective’s targeted alpha-particle therapy PSV359 in co...
REVOLUTIONIZING HEALTHCARE: Tempus partners with Merck on AI-driven precision medicine
Tempus CEO Eric Lefkofsky discusses the company's artificial intelligence-driven precision medicine partnership with Merck on ‘The Claman Countdown.'
Merck price target raised to $172 from $150 at HSBC
HSBC raised the firm’s price target on Merck (MRK) to $172 from $150 and keeps a Buy rating on the shares. The firm adjusted targets in the healthcare group to…
Merck & Co. Transcript: Wells Fargo 21st Annual Healthcare Conference
Significant progress was reported in portfolio transformation, with projected human health revenues rising to over $70B by the mid-2030s. Oncology and non-oncology pipelines are advancing, with new launches, robust clinical data, and strategic investments supporting long-term growth.
The Big 3: ROST, MRK, AAPL
Don Kaufman (@Theotrade) calls the U.S. Treasury's $6 billion bond buyback plan "nominal" to investors seeking relief as the inflation picture gets wider by the day. However, he sees bearish opportuni...
AI & Robotics in 2026: 16 Recent Developments for Investors
If AI and robotics suddenly feel like they are moving faster, August gave investors plenty of evidence that the pace really is accelerating. We saw longer-running agents, faster and cheaper inference,...
Leerink ups Merck price target on pipeline momentum
Leerink analyst Daina Graybosch raised the firm’s price target on Merck (MRK) to $161 from $127 and keeps an Outperform rating on the shares. The firm cites Merck’s “strong” pipeline…
Merck price target raised to $161 from $127 at Leerink
Leerink raised the firm’s price target on Merck (MRK) to $161 from $127 and keeps an Outperform rating on the shares.
Merck price target raised to $170 from $146 at Guggenheim
Guggenheim raised the firm’s price target on Merck (MRK) to $170 from $146 and keeps a Buy rating on the shares, driven mainly by increased sales estimates for intismeran autogene…