Merck & Co., Inc.

MRK
· NYSE
Analyzed 2026-07-2128 days sinceGenerated by FomoLog Agent
FOMO Score
+9.30%
+$11.57 · per share
Report-date close → Current (2026-08-17)
$124.40$135.97
Days Held
28d
Price As Of
2026-08-17
Not investment adviceThis is not investment advice. FomoLog provides factual summaries and post-hoc price-change context only. Investment decisions and their outcomes are solely the responsibility of the investor.Legal Notice ↗

Price Trend

Report date → now · daily close
$120$125$130$135$140Jul 20Jul 29Aug 6Aug 17Report date $124.40Current $135.97

Summary

As of July 2026, Merck is a global pharmaceutical company with an oncology and vaccine portfolio centered on the immuno-oncology drug Keytruda, and reported Q2 2026 revenue of $25.310 billion (+6.6% year over year) and Non-GAAP adjusted EPS of $2.90 (+4.7% year over year). Over the same period, Keytruda saw continued regulatory and clinical progress, including meeting the primary endpoint in a Phase 3 endometrial cancer trial (7/15), an expanded bladder cancer indication approval (7/10), and approval of the oral PCSK9 inhibitor LIPFENDRA (7/16). The 2026-07-20 close was $124.40, down -2.43% from the prior close of $127.50, with volume of 7,729,047 shares.

Price-Change Context Note

No Merck-specific disclosure event (such as a clinical trial failure or regulatory rejection) was identified from primary sources on the decline date of 2026-07-20; what was confirmed was a downward revision of consensus earnings estimates and a rating change from a small research firm, both largely secondary-source in nature (ahead of the quarterly earnings release scheduled for 2026-08-04). Trading volume that day (7,729,047 shares) was below the recent average volume (approximately 9.90-10.36 million shares).

Key Facts

Q2 2026 revenue of $25.310 billion (+6.6% YoY), Non-GAAP adjusted EPS of $2.90 (+4.7%)
Keytruda Phase 3 endometrial cancer trial (KEYNOTE-C93) met primary endpoint (7/15); expanded combination-therapy bladder cancer indication approved (7/10); oral PCSK9 inhibitor LIPFENDRA approved (7/16)
2026-07-20 close $124.40, down -2.43% from prior close, volume of 7,729,047 shares (below recent average)
Short interest 1.27% of float (FINRA, 2026-06-30 settlement date); institutional ownership 76.07% (13F aggregation)
Keytruda accounted for approximately 46% of total company revenue in 2024; core patents expire around 2028-2029
Trailing P/E 34.79x, Forward P/E 20.31x, EV/EBITDA 11.88x (as of 2026-07-21)

Theme Relevance

#Dividend Stocks
2/5
#Tariffs & Trade
2/5
#Biotech & Pharma
5/5

Full Analysis

Merck & Co., Inc. (MRK)
NYSE · Analysis date 2026-07-21 · Reference close 124.40 USD (2026-07-20) · Previous close 127.50 USD · Change on reference date -2.43%

Factual Summary

Merck & Co., Inc. (known as MSD outside the United States and Canada) is a pharmaceutical company headquartered in Rahway, New Jersey, with an oncology, vaccine, and cardiovascular portfolio built around its core immuno-oncology product Keytruda (pembrolizumab). Second-quarter 2026 revenue was $25.310 billion (+6.6% year over year), with Non-GAAP adjusted EPS of $2.90 (+4.7% year over year).

Price-Change Context Note

No Merck-specific disclosure event was identified from primary sources on the decline date of 2026-07-20; what was confirmed was a downward revision of consensus earnings estimates and a rating change from a small research firm, both largely secondary-source in nature (ahead of the quarterly earnings release scheduled for 2026-08-04). Trading volume that day (7,729,047 shares) was below the recent average volume (approximately 9.90-10.36 million shares).

Business Overview & Recent Pipeline

  • 2026-07-16: FDA approval of LIPFENDRA (enlicitide), an oral once-daily PCSK9 inhibitor — the CORALreef Lipids trial showed a 56% reduction in LDL-C at 24 weeks versus placebo.
  • 2026-07-15: KEYTRUDA Phase 3 trial (KEYNOTE-C93) met its primary progression-free survival endpoint in advanced/recurrent mismatch repair-deficient (MMR-deficient) endometrial cancer.
  • 2026-07-10: FDA approved an expanded indication for KEYTRUDA and KEYTRUDA QLEX in combination with PADCEV for perioperative treatment of muscle-invasive bladder cancer.
  • 2026-03-25: Announced the acquisition of Terns Pharmaceuticals ($53 per share in cash, total equity value of approximately $6.7 billion).

Not available: segment-level revenue breakdown (pharmaceuticals/animal health) and certain fiscal year 2026 figures (excluded from this report due to conflicting figures across research sources).

5-Year Financial Trend

5-Year Revenue Trend (USD Billions)
Merck Annual Revenue 2021-202548.759.360.164.265.020212022202320242025
Fiscal year (FY) basis · Source: aggregated from annual reports (stockanalysis.com, A) · Research date 2026-07-21
5-Year Net Income Trend (USD Billions)
Merck Annual Net Income 2021-202513.014.50.417.118.320212022202320242025
Based on Net Income Attributable to Merck · Primarily driven by a surge in R&D expense in 2023 ($13.548B→$30.531B) · Source: stockanalysis.com/10-K (A) · Research date 2026-07-21

Revenue rose steadily from $48.704 billion in 2021 to $65.011 billion in 2025 (a CAGR of approximately 7.5%). Net income in 2023 fell sharply to $0.365 billion due to a surge in R&D expense, then recovered to $17.117 billion and $18.254 billion in 2024-2025 as R&D expense normalized from $17.938 billion to $15.789 billion.

Peer Comparison

Peer Forward P/E Comparison (x)
MRK vs. Peers Forward P/E20.38.79.831.820.5MRKPFEBMYLLYJNJ
As of 2026-07-21 · Source: stockanalysis.com (A) · MRK highlighted only
CompanyP/E (Trailing)P/E (Forward)EV/EBITDAMarket Cap
Merck (MRK)34.7920.3111.88$307.25B
Pfizer (PFE)18.898.717.57$141.06B
Bristol-Myers Squibb (BMY)16.849.828.35$122.85B
Eli Lilly (LLY)40.7431.8329.28$1.02T
Johnson & Johnson (JNJ)28.8420.5318.14$598.96B

As of 2026-07-21 (stockanalysis.com, A). Merck trades at a premium to industry peers on a trailing P/E basis, but its Forward P/E (20.31x) is closer to JNJ's (20.53x).

Valuation (Factual Multiples)

P/E (Trailing)
34.79x
As of 2026-07-21 (A)
P/E (Forward)
20.31x
As of 2026-07-21 (A)
EV/EBITDA
11.88x
As of 2026-07-21 (A)
P/B
6.70x
As of 2026-07-21 (A)
Dividend Yield
2.73%
As of 2026-07-21 (A)
Market Cap
$307.25B
As of 2026-07-21 (A)

A P/B of 6.70x is high relative to book equity; this reflects an industry characteristic of pharmaceuticals in which intangible assets such as patents and pipeline value are not fully captured on the balance sheet.

Supply and Demand Trends

Short Interest (% of Float)
1.27%
FINRA settlement date 2026-06-30 (A, secondary aggregation)
Institutional Ownership
76.07%
13F aggregation (A, secondary aggregation)
Put/Call Volume Ratio
0.42
Snapshot, reference date unclear (A)
Volume (7/20)
7,729,047 shares
Below recent average (A)

Trading volume on 2026-07-20 (7,729,047 shares) was below the recent average volume (approximately 9.90-10.36 million shares). Short interest as a share of float rose 3.68% versus the prior settlement date. Over the trailing 12 months, aggregate institutional buy transactions (2,576 transactions, $31.19B) exceeded sell transactions (2,121 transactions, $18.16B) in count and value, though this quarterly-disclosure-based data lags day-to-day flow. Insider (Form 4) filings over the past six months were predominantly stock option exercises, tax withholding, and annual compensation-related acquisitions; no open-market stock dispositions by insiders were identified.

Corporate Governance

Independent Director Ratio
92.3%
12 of 13 directors, DEF 14A 2026-04-08 (A)
Largest Reported Shareholder (BlackRock)
8.0%
SC 13G/A filed 2024-01-26, updated filing not available (A)
2025 Share Buybacks
$5,084M
10-K, up from $1,306M in the prior year (A)
2025 Dividends Declared per Share
$3.28
10-K, up from $3.12 in 2024 (A)

The board combines the Chair and CEO roles (Robert M. Davis), but maintains an independent lead director (Thomas H. Glocer) and staffs all four standing committees entirely with independent directors. At the 2026-05-26 annual meeting, all 13 directors were re-elected (with approval rates of roughly 88-99.7%). BlackRock's 8.0% stake is from the most recent SC 13G/A filed on EDGAR (2024-01-26); Vanguard's prior 9.66% stake (as of 2024-02-13) has no confirmed subsequent update, so its current ownership percentage is not available.

Macro Environment

FactorCurrent ValueReference Date
US Federal Funds Rate3.50-3.75%2026-06-17 FOMC (A)
US 10-Year Treasury Yield4.57%2026-07-20 (A)
US Dollar Index (DXY)100.7-100.82026-07-20 (A)
Healthcare Sector (XLV)161.092026-07-19 (A)

Merck derives roughly 44% of revenue from outside the US (based on the first nine months of 2025), giving it significant currency exposure — a weaker dollar is factually positive for the dollar-translated value of revenue and earnings. Under Medicare drug price negotiation (IRA), Januvia's 2026 30-day supply price has been cut 79%, from $527 to $113, and Keytruda is scheduled to enter negotiation starting in 2028. Under the tariffs on branded pharmaceuticals stemming from the 2026-04-02 executive order, Merck secured an exemption through 2029-01-20 via an MFN and onshoring agreement.

Risk Factors (Factual)

  • Keytruda accounted for approximately 46% of total company revenue in 2024 and is the company's core product; its active-ingredient patent is scheduled to expire around 2028-2029.
  • Keytruda has been selected for 2026 Medicare drug price negotiation, with the new price scheduled to take effect from January 2028.
  • 2025 Gardasil revenue declined approximately 39% year over year due to a shipment halt tied to excess distributor inventory at Chinese partner Zhifei.
  • Tariffs on branded pharmaceuticals (up to 100%) stemming from the 2026-04-02 executive order were exempted for Merck through 2029-01-20 via an MFN and onshoring agreement signed 2025-12-19, in exchange for a committed $70 billion in US manufacturing investment.
  • In fiscal year 2023, a surge in R&D expense from $13.548 billion to $30.531 billion in the prior year drove operating income down sharply from $17.945 billion to $2.355 billion.
  • On 2026-07-01/02, Phase 2 trials of an Alzheimer's treatment (MK-1167) co-developed with partner Neuphoria Therapeutics were terminated early for lack of efficacy.

Theme Relevance

Immuno-oncology
5
Patent Cliff
4
Pharmaceutical Tariff Policy
2
Dividend Stocks
2
#Tariffs & Trade Under tariffs on branded pharmaceuticals (up to 100%) stemming from the 2026-04-02 executive order, Merck secured an exemption through 2029-01-20 via an MFN and onshoring agreement signed 2025-12-19, in exchange for a committed $70 billion in US manufacturing investment.
#Biotech & Pharmaceuticals Built around the core product Keytruda (pembrolizumab), Merck holds an oncology and vaccine portfolio, with continued clinical and regulatory progress in July 2026 including a Phase 3 endometrial cancer trial (KEYNOTE-C93) meeting its primary endpoint (7/15), an expanded bladder cancer indication approval (7/10), and approval of the PCSK9 inhibitor LIPFENDRA (7/16).
Merck's dividend yield was 2.73% as of 2026-07-21, and 2025 dividends declared per share of $3.28 increased from $3.12 in 2024.

Fact Highlights

Q2 2026 revenue of $25.310 billion (+6.6% YoY), Non-GAAP adjusted EPS of $2.90 (+4.7% YoY)
Keytruda Phase 3 endometrial cancer trial met primary endpoint (7/15) · bladder cancer indication expanded (7/10) · LIPFENDRA newly approved (7/16)
2026-07-20 close $124.40, down -2.43% from prior close, volume below recent average
Short interest 1.27% (FINRA 6/30), institutional ownership 76.07% (13F)
Keytruda accounted for approximately 46% of total revenue in 2024; core patents expire around 2028-2029
Trailing P/E 34.79x, Forward P/E 20.31x, EV/EBITDA 11.88x (2026-07-21)

This is not investment advice. FomoLog provides factual summaries and post-hoc price-change context only. Investment decisions and their outcomes are solely the responsibility of the investor.

Generated by FomoLog Agent · Data sources: KRX · NASDAQ · DART · SEC EDGAR