$AMGN

AMGEN INC (AMGN): Results of Operations and Financial Condition

AMGEN INC (AMGN) filed an SEC Form 8-K — Results of Operations and Financial Condition. Exhibit 99.1 News Release One Amgen Center Drive Thousand Oaks, CA 91320-1799 Telephone 805-447-1000 www.amgen.com AMGEN REPORTS SECOND QUARTER 2026 FINANCIAL RESULTS THOUSAND OAKS, Calif. (Aug. 4, 2026) - Amgen (NASDAQ:AMGN) today announced financial results for the second quart

Original reporting
Published Aug 4, 2026, 8:03 PM UTC
Analysis
alphai AI DeskAI-generated
Added to alphai Aug 4, 2026, 8:08 PM UTC. Informational, not investment advice.
How this was made
alphai summarizes source reporting and applies a structured AI analysis for relevance, timing, sentiment and ticker impact. Always verify material claims with the original publisher.
alphai market briefEarnings
Primary signal
$AMGN
Bullish
medium confidence
Mentioned
$AMGN
Relevance
8/10
alphai data visualization · based on SEC EDGAR 8-K
Decision brief

The 30-second read

$AMGNBullishMed
01

Why it matters

Traders can use the reported revenue, GAAP and non-GAAP EPS, operating margin, and free cash flow to reprice near-term expectations and reassess product momentum across growth and established franchises.

02

Market read

A primary earnings release with multiple hard financial metrics and product-level growth/decline details, likely to influence short-term positioning and estimate revisions.

03

What to watch

Non-GAAP operating margin fell 0.5 points and free cash flow comparisons include a repatriation tax payment timing effect, so cash strength may not be purely operational.

Relevance 8/10Novelty 8/10Timing: after-hours filing today, Aug. 4, 2026
alphai · Earnings readAMGN · second quarter of 2026 · ended June 30, 2026

AMGEN REPORTS SECOND QUARTER 2026 FINANCIAL RESULTS

Solid quarter

Total revenues increased 10% to $10.1 billion, product sales grew 9%, GAAP EPS increased 65% to $4.37, and free cash flow rose to $3.5 billion. Non-GAAP operating margin decreased 0.5 percentage points and several mature products declined amid biosimilar competition and pricing pressure.

Revenue
$10.1 billion
10% y/y
Repatha
$953 million
37% y/y
Operating margin · GAAP
36.8%
6.5 percentage points y/y
EPS · non-GAAP
$6.29
4% y/y

Key metrics

as reported
MetricValueq/qy/y
Total revenuesGAAP$10.1 billion10%
Total product salesGAAP$9,537 million9%
GAAP earnings per shareGAAP$4.3765%
Non-GAAP earnings per sharenon-GAAP$6.294%
GAAP operating incomeGAAP$3.5 billion
Non-GAAP operating incomenon-GAAP$4.6 billion
GAAP cost of salesGAAP$2,811 million(7%)
Non-GAAP cost of salesnon-GAAP$1,874 million21%
GAAP cost of sales as a percentage of product salesGAAP29.5 %(4.8) pts.
Non-GAAP cost of sales as a percentage of product salesnon-GAAP19.6 %1.9 pts.
GAAP Research & Development expensesGAAP$1,868 million7%
Non-GAAP Research & Development expensesnon-GAAP$1,851 million10%
GAAP Research & Development expenses as a percentage of product salesGAAP19.6 %(0.3) pts.
Non-GAAP Research & Development expenses as a percentage of product salesnon-GAAP19.4 %0.2 pts.
GAAP Selling, General & Administrative expensesGAAP$1,745 million3%
Non-GAAP Selling, General & Administrative expensesnon-GAAP$1,717 million4%
GAAP Selling, General & Administrative expenses as a percentage of product salesGAAP18.3 %(1.0) pts.
Non-GAAP Selling, General & Administrative expenses as a percentage of product salesnon-GAAP18.0 %(0.8) pts.
GAAP other operating expensesGAAP$116 million51%
GAAP total operating expensesGAAP$6,540 million0%
Non-GAAP total operating expensesnon-GAAP$5,442 million11%
GAAP operating marginGAAP36.8%6.5 percentage points
Non-GAAP operating marginnon-GAAP48.4%(0.5) percentage points
GAAP tax rateGAAP14.2 %5.5 pts.
Non-GAAP tax ratenon-GAAP15.6 %1.4 pts.
Free cash flownon-GAAP$3.5 billion
Cash and cash equivalentsGAAP$14.0 billion
Debt outstandingGAAP$57.3 billion

Segments

SegmentRevenueq/qy/y
RepathaVolume growth.$953 million37%
EVENITYVolume growth.$714 million38%
Prolia20% lower volume and 12% lower net selling price as multiple biosimilars have launched globally with more biosimilars expected.$759 million(32%)
TEPEZZAPrimarily driven by 6% higher net selling price and 6% volume growth.$576 million14%
KRYSTEXXA23% higher net selling price, partially offset by lower inventory levels.$400 million15%
UPLIZNAPrimarily driven by volume growth.$335 million90%
TAVNEOSVolume growth.$150 million36%
Ultra-Rare productsPROCYSBI, RAVICTI, ACTIMMUNE, BUPHENYL, and QUINSAIR.$149 million(19%)
TEZSPIREVolume growth.$486 million42%
OtezlaPrimarily driven by 9% lower net selling price and 6% lower volume.$491 million(21%)
EnbrelPrimarily driven by 22% lower net selling price, partially offset by 16% favorable changes to estimated sales deductions. The decline in net selling price reflects the impact of U.S. Medicare Part D price setting under the Inflation Reduction Act, effective January 1, 2026, as well as an increased 340B Program mix.$580 million(4%)
AMJEVITA/AMGEVITAPrimarily driven by volume growth.$155 million17%
PAVBLUPrimarily driven by volume growth based on its position as the only commercially available biosimilar to EYLEA in the U.S. during this period.$287 millionChange in excess of 100%
WEZLANA/WEZENLANot provided.$61 million74%
BLINCYTOPrimarily driven by 16% volume growth.$472 million23%
IMDELLTRA/IMDYLLTRAPrimarily driven by volume growth.$288 millionChange in excess of 100%
VectibixPrimarily driven by volume growth.$338 million11%
KYPROLISLower volume.$314 million(17%)
LUMAKRAS/LUMYKRASPrimarily driven by volume growth.$111 million23%
Nplate13% volume growth and higher net selling price.$430 million17%
XGEVAPrimarily driven by 22% lower volume and 8% lower net selling price as multiple biosimilars have launched globally with more biosimilars expected.$352 million(34%)
MVASI16% lower net selling price and lower volume.$153 million(20%)
AranespNot provided.$352 million(2%)
NeulastaNot provided.$179 millionChange in excess of 100%
ParsabivNot provided.$101 million10%
Other productsAimovig, AVSOLA, KANJINTI, EPOGEN, BKEMV/BEKEMV, RIABNI, IMLYGIC, NEUPOGEN, RAYOS, DUEXIS, Sensipar/Mimpara, Corlanor, and PENNSAID.$351 million5%
BiosimilarsBiosimilars total $199 million in Q2 ’26 and $172 million in Q2 ’25.$199 million
Rare Disease productsRare Disease products total ($3) million in Q2 ’26 and $4 million in Q2 ’25.($3) million
Established products15% higher net selling price and 2% volume growth.$632 million19%

Capital returns

  • The Company declared a second quarter 2026 dividend on March 4, 2026 of $2.52 per share that was paid on June 5, 2026 to all stockholders of record as of May 15, 2026, representing a 6% increase from the same period in 2025.
  • During the second quarter of 2026, there were no repurchases of shares of common stock under our stock repurchase program.

What drove it

  • Product sales grew 9%, driven by volume growth.
  • Twenty-two products delivered at least double-digit sales growth in the second quarter.
  • Seventeen products are annualizing at more than $1 billion based on second quarter sales.
  • The six key growth drivers grew 26% year over year, generating nearly 70% of second-quarter product sales.
  • GAAP cost of sales as a percentage of product sales decreased 4.8 percentage points, driven by lower amortization expense from acquisition-related assets, partially offset by higher profit share expense, higher manufacturing costs and changes in sales mix.
  • Free cash flow increased reflecting the final repatriation tax payment in the second quarter of 2025 and current period business performance, partially offset by timing of working capital.

Concerns

  • Non-GAAP operating margin decreased 0.5 percentage points to 48.4%.
  • Non-GAAP total operating expenses increased 11% year-over-year, including a 10% increase in R&D expenses.
  • Prolia sales decreased 32% and XGEVA sales decreased 34% as multiple biosimilars have launched globally with more biosimilars expected.
  • Enbrel sales decreased 4%, reflecting U.S. Medicare Part D price setting under the Inflation Reduction Act and an increased 340B Program mix.
  • Otezla sales decreased 21%, KYPROLIS sales decreased 17%, and MVASI sales decreased 20%.

What to watch

  • Volume growth across Repatha, EVENITY, UPLIZNA, TEZSPIRE, PAVBLU, BLINCYTO and IMDELLTRA.
  • The impact of biosimilar launches on Prolia and XGEVA sales.
  • R&D spending in Later-Stage Clinical Programs, primarily those related to MariTide, and Marketed Product Support.
  • The effect of higher profit share expense, manufacturing costs and sales mix on non-GAAP cost of sales and operating margin.
  • TAVNEOS engagement with the U.S. Food and Drug Administration.

Balance sheet and cash flow

  • The Company generated $3.5 billion of free cash flow in the second quarter of 2026 versus $1.9 billion in the second quarter of 2025.
  • Cash and cash equivalents totaled $14.0 billion and debt outstanding totaled $57.3 billion as of June 30, 2026.

Analysis

Amgen reported total revenues of $10.1 billion, up 10%, while total product sales increased 9% to $9,537 million. The release attributes product-sales growth to volume growth, with twenty-two products delivering at least double-digit sales growth. Repatha, EVENITY, UPLIZNA, TEZSPIRE, PAVBLU, BLINCYTO and IMDELLTRA were among the products posting material growth.

The sales mix also contains substantial pressure points. Prolia sales decreased 32% and XGEVA sales decreased 34%, with both declines tied to lower volume and lower net selling price following global biosimilar launches. Enbrel sales decreased 4%, driven primarily by lower net selling price associated with U.S. Medicare Part D price setting under the Inflation Reduction Act and a higher 340B Program mix. Otezla, KYPROLIS and MVASI also posted year-over-year sales declines.

Profitability was stronger on a GAAP basis but softer on a non-GAAP margin basis. GAAP operating income increased from $2.7 billion to $3.5 billion, GAAP operating margin increased 6.5 percentage points to 36.8%, and GAAP EPS increased from $2.65 to $4.37. Lower amortization expense from acquisition-related assets helped reduce GAAP cost of sales as a percentage of product sales by 4.8 percentage points. Non-GAAP operating income increased from $4.3 billion to $4.6 billion and non-GAAP EPS increased from $6.02 to $6.29, but non-GAAP operating margin decreased 0.5 percentage points to 48.4% as non-GAAP operating expenses increased 11%.

Cash generation improved materially, with free cash flow of $3.5 billion versus $1.9 billion. The company attributed the increase to the final repatriation tax payment in the second quarter of 2025 and current-period business performance, partly offset by working-capital timing. Amgen paid a $2.52 per share dividend, representing a 6% increase from the same period in 2025, made no share repurchases during the quarter, and reported $14.0 billion of cash and cash equivalents against $57.3 billion of debt outstanding. The filing provided no forward guidance.

Management, verbatim

Our results demonstrate strong performance across our business. Our six key growth drivers grew 26% year over year, generating nearly 70% of second-quarter product sales. As we expand the potential of our existing medicines through new indications and advance the next wave of pipeline molecules through Phase 3, we remain confident in our ability to deliver growth well into the next decade.

Robert A. Bradway, chairman and chief executive officer

Not in the filing

stated, not guessed
  • Forward guidance for revenue, gross margin, operating expenses, tax rate, EPS, cash flow, capital returns and other metrics.
  • Prior guidance for comparison.
  • GAAP net income and non-GAAP net income.
  • Operating cash flow and capital expenditures.
  • Gross margin.
  • Prior-quarter comparisons for reported operating metrics and product sales.
  • Prior-year dollar amount for total revenues.
  • Prior-year cash and debt balances.

AlphaAI analysis generated from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure was cross-checked against the filing text; consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

Background

The document is Amgen’s SEC Form 8-K for Q2 2026 results, filed with an earnings release exhibit (Ex-99.1).

Company-level read

Ticker impact

$AMGNBullishMedium confidence
Context

Amgen reported Q2 2026 results with total revenues up 10% to $10.1B, GAAP EPS up 65% to $4.37, and $3.5B free cash flow.

Expected impact

Likely supportive for the stock versus prior expectations, with upside bias if investors focus on GAAP EPS and free cash flow strength.

Evidence & confidence

This is a primary earnings release filed on Form 8-K, including multiple hard numbers (revenue, EPS, operating margin, and free cash flow) plus notable product growth/declines (e.g., Repatha, Evenity, Prolia, Enbrel).

Market effects

Biopharma large-cap sentiment may improve if investors view Amgen’s growth drivers and cash generation as resilient despite biosimilar pressure in parts of the portfolio.

Limited direct regional spillover; primarily US large-cap healthcare sentiment.

Product sales and biosimilar dynamics are relevant to global pharma peers, but the article is company-specific.

Counterpoint

Despite strong headline growth, several major products declined (e.g., Prolia, XGEVA, Enbrel net selling price pressure), which could cap multiple expansion if investors extrapolate biosimilar erosion.

Key entities

  • Amgen

    NASDAQ-listed biopharmaceutical company reporting Q2 2026 financial results and product sales performance.

  • FDA

    Referenced in the release regarding engagement and clinical effectiveness/balance of benefit-risk for TAVNEOS.

Every AMGN earnings report

This story covers one filing. The ticker page keeps them all: each quarter's reported metrics with year-over-year and sequential comparisons, segments, guidance, and how the numbers landed against the company's own prior outlook.

Related articles

$AMGNMed

Amgen Slides as Tavneos Regulatory Pressure Weighs on Sentiment

Amgen (AMGN) shares fell 6.8% after U.K. regulators suspended Tavneos for new patients, citing concerns about its efficacy. The FDA also proposed withdrawing the drug in the U.S., raising regulatory risks. Tavneos contributes a small portion of Amgen's revenue. Insider sales, hedge fund activity, and analyst price targets were also noted.

$AMGNMedAI 8/10

Amgen (AMGN) Says Repatha Reduced Mortality Before a First Heart Attack or Stroke. Can Earlier Use Expand the Market?

Amgen (AMGN) reported Repatha reduced all-cause mortality by 20% in a secondary analysis of the VESALIUS-CV trial. The study involved over 12,000 high-risk adults without prior heart attacks or strokes. Repatha also lowered cardiovascular risks and LDL-C levels. Amgen aims to expand use before first major cardiovascular events, citing 15 years of clinical trials and global use in 9 million patients.

$NVSHighAI 8/10

NVS, IONS, AMGN Stocks Drop After-Hours — What’s Driving The Selloff?

Novartis (NVS) and Ionis (IONS) shares dropped after-hours Friday after a heart-disease trial for pelacarsen failed to show reduced risk of heart attacks or strokes, despite lowering lipoprotein(a). NVS fell 7%, IONS 10%. Amgen (AMGN) also dropped 5% as it develops a similar drug. NVS closed at $159.99. Both NVS and IONS have seen significant YTD changes, up 16% and down 27% respectively.

$AZNMedAI 8/10

Topline results: Tezepelumab improves dysphagia frequency, severity in EoE

AstraZeneca and Amgen reported positive phase 3 trial results for tezepelumab (Tezspire) in treating eosinophilic esophagitis (EoE). The study showed improved dysphagia and histologic remission at weeks 24 and 52 compared to placebo. The companies plan to share data with regulators. Tezspire is already FDA-approved for severe asthma and chronic rhinosinusitis.

$AZNMedAI 8/10

AstraZeneca, Amgen Drug Hits Phase III EoE Goals

AstraZeneca and Amgen's TEZSPIRE met primary endpoints in a Phase III trial for eosinophilic esophagitis, showing significant improvements in histologic remission and dysphagia symptoms. The drug maintained efficacy through 52 weeks, with results planned for regulatory submission. TEZSPIRE is approved for severe asthma and chronic rhinosinusitis with nasal polyps.

$AMGNMed

Wells Fargo raises Amgen stock price target to $435 on drug trial outlook

Wells Fargo raised its price target for Amgen (AMGN) to $435, citing upcoming drug trial results. The stock is near its 52-week high and has gained 63% over the past year. A positive trial could add $10-$15 per share, while a negative result could reduce it by $20-$25. Amgen reported strong Q2 2026 earnings, with revenue of $10.1B and EPS of $6.29, exceeding estimates. Analysts remain optimistic despite a regulatory setback for its drug Tavneos.