Merck & Co., Inc. (TSX:MRK)
Canada · Delayed Price · Currency is CAD | Market Cap | 450.70B +61.7% |
| Revenue (ttm) | 91.80B +2.9% |
| Net Income | 12.47B -48.8% |
| EPS | 4.99 -48.0% |
| Shares Out | n/a |
| PE Ratio | 36.14 |
| Forward PE | 20.78 |
| Dividend | 0.76 (2.64%) |
| Ex-Dividend Date | Jun 15, 2026 |
| Volume | 4,300 |
| Open | 28.92 |
| Previous Close | 28.88 |
| Day's Range | 28.41 - 28.98 |
| 52-Week Range | 17.55 - 28.98 |
| Beta | n/a |
| Analysts | n/a |
| Price Target | n/a |
| Earnings Date | Aug 4, 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 terminates Phase 2 Alzheimer’s study
Merck (MRK) has terminated a Phase 2 randomized, placebo-controlled study that was intended to evaluate the efficacy and safety of MK-1167 as adjunctive therapy in participants with mild to moderate…
Merck to Hold Second-Quarter 2026 Sales and Earnings Conference Call Aug. 4
RAHWAY, N.J.--(BUSINESS WIRE)--Merck to Hold Second-Quarter 2026 Sales and Earnings Conference Call Aug. 4.
Merck price target raised to $155 from $136 at Scotiabank
Scotiabank raised the firm’s price target on Merck (MRK) to $155 from $136 and keeps an Outperform rating on the shares. The increase in price target is driven by multiple…
House committee opens probe into Merck, AbbVie China drug trials, Reuters says
A bipartisan group of U.S. lawmakers has opened national security investigations into whether drugmakers Merck (MRK) and AbbVie (ABBV) have been involved in clinical trials conducted in China that hel...
Merck price target raised to $141 from $130 at BofA
BofA raised the firm’s price target on Merck (MRK) to $141 from $130 and keeps a Buy rating on the shares, citing a sector re-rating for the firm’s raised target.
US House committee opens investigation into Merck, AbbVie China drug trials
The chair of the U.S. House Select Committee on China opened national security investigations into whether five drugmakers including Merck and AbbVie have been involved in clinical trials conducted i...
Merck & Company (MRK) Price Forecast: Can Momentum Drive New Highs?
Merck extends its bullish breakout from a pennant pattern, supported by strong volume and higher swing lows, with technical structure pointing toward continued upside potential.
Merck price target raised to $155 from $136 at Scotiabank
Scotiabank raised the firm’s price target on Merck (MRK) to $155 from $136 and keeps an Outperform rating on the shares.
Merck Announces New Agreement with ADAP Crisis Task Force to Improve Access and Care for People Living with HIV
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck Announces Agreement to Improve Treatment Access for People Living with HIV. Agreement will help state ADAP programs provide access to IDVYNSO.
The Big 3: JPM, DHR, MRK
Dan Deming talks joins today's Big 3 and highlights JPMorgan Chase (JPM) as shares touch new record highs. He sees Danaher (DHR) as a candidate for a continuing breakout, noting a similar pattern in M...
Merck says FDA approves Keytruda and Keytruda Qlex in combo with Trodelvy
Merck (MRK) announced the U.S. FDA approved Keytruda and Keytruda Qlex, each in combination with Trodelvy, Gilead’s (GILD) Trop-2-directed antibody-drug conjugate, for the first-line treatment of adul...
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)
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) approved KEYTRUDA® (pe...
Merck says EC approves Keytruda plus Padcev combination
Merck (MRK) announced that Keytruda, Merck’s anti-PD-1 therapy, in combination with Padcev, an antibody-drug conjugate, is approved in the European Union, as neoadjuvant treatment and then continued a...
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
RAHWAY, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that KEYTRUDA® (pembrolizumab), Merck's anti-PD-1 therapy, in combination with P...
Merck initiated with an Outperform at CICC
CICC initiated coverage of Merck (MRK) with an Outperform rating and $138 price target
Merck and Mae Partner to Expand Doula Workforce and Address Maternal Health Disparities in High-Risk U.S. Markets
NEW YORK--(BUSINESS WIRE)--Merck, through the company's Merck for Mothers initiative, and Mae are collaborating on a multi-state effort to expand and sustain the community-based doula workforce, with ...
Merck's bowel disease drug meets main goal in late-stage trial
Merck said on Monday its drug met the main goal in a late-stage trial testing it in patients with a type of inflammatory bowel disease.
Merck announces ‘positive’ results from Phase 3 trial of tulisokibart
Merck (MRK) announced positive topline results from the Phase 3 ATLAS-UC induction-only study evaluating tulisokibart, an investigational humanized monoclonal antibody targeting tumor necrosis factor-...
Merck's Tulisokibart Met Primary and Key Secondary Endpoints in the Phase 3 ATLAS-UC Induction-only Study in Patients With Moderately to Severely Active Ulcerative Colitis (UC)
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced positive topline results from the Phase 3 ATLAS-UC induction-only ...
Merck says FDA approves additional indication for Capvaxive
Merck (MRK) announced that the U.S. FDA has approved an expanded indication for Capvaxive to include children and adolescents aged 2 through 17 years who have completed a primary pediatric…
Merck's pneumococcal vaccine wins US approval for high-risk children, teens
Drugmaker Merck said on Thursday the U.S. health regulator has approved an expanded use of its pneumococcal vaccine for children and teenagers who face a higher risk of catching the bacterial diseas...
U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) in Children and Adolescents Aged 2 through 17 at Increased Risk for Pneumococcal Disease
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine).
Study Reveals Dog Owners and Veterinarians See Challenges in Treating Allergic Skin Disease, Highlighting a Need for a Targeted Rapid Onset Treatment for Dogs of All Ages
RAHWAY, N.J.--(BUSINESS WIRE)--Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), today announced r...
Protillion Biosciences Announces Drug Discovery Collaboration with Merck
CARLSBAD, Calif.--(BUSINESS WIRE)--Protillion Biosciences, Inc., a leader in lab-in-the-loop AI drug design, today announced the signing of a multi-target discovery collaboration and license agreement...
FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With WELIREG® (belzutifan), for Adjuvant Treatment of Certain Patients With Clear Cell Renal Cell Carcinoma (ccRCC)
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--FDA Approves KEYTRUDA® and KEYTRUDA QLEXTM , Each With WELIREG®, for Adjuvant Treatment of Certain Patients With ccRCC.