$LLY

ELI LILLY & Co (LLY): Lilly reports second-quarter 2026 financial results, raises full-year guidance, and highlights continued growth and pipeline progress

ELI LILLY & Co (LLY) filed an SEC Form 8-K — Results of Operations and Financial Condition. August 5, 2026 For release: Immediately Refer to: Megan MacCauley; maccauley_megan@lilly.com (Media) Mike Czapar; czapar_michael_c@lilly.com (Investors) Lilly reports second-quarter 2026 financial results, raise s full-year guidance, and highlights continued growth and pipeline p

Original reporting
Published Aug 5, 2026, 11:05 AM UTC
Analysis
AlphAI AI DeskAI-generated
Added to AlphAI Aug 5, 2026, 11:34 AM 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
$LLY
Bullish
high confidence
Mentioned
$LLY
Relevance
9/10
AlphAI data visualization · based on SEC EDGAR 8-K
Decision brief

The 30-second read

$LLYBullishHigh
01

Why it matters

The filing provides a complete earnings and guidance package with quantified EPS and revenue changes, plus specific regulatory approvals and pipeline trial progress that can drive near-term sentiment and positioning.

02

Market read

A same-day earnings and guidance update with multiple quantified catalysts (revenue/EPS growth, raised guidance, and regulatory approvals) makes this a direct driver for LLY trading and options repricing.

03

What to watch

Investors may focus on the quality of growth (volume vs price), the tax impact from non-deductible acquired IPR&D, and how much of the guidance strength is attributable to business development timing versus core demand.

Relevance 9/10Novelty 9/10Timing: pre-market today (SEC 8-K filed Aug 5, 2026)
AlphAI · Earnings readLLY · Q2 2026

Lilly reports second-quarter 2026 financial results, raises full-year guidance, and highlights continued growth and pipeline progress.

✓Strong quarter

Revenue increased 48% to $23.0 billion, reported EPS increased 26% to $7.94, and the company increased 2026 full-year revenue guidance to $85.0 billion to $87.0 billion. Growth was led by Mounjaro and Zepbound volume, while gross-margin expansion persisted despite lower realized prices and acquisition-related charges.

Revenue
$23.0B
48% y/y
Mounjaro
$9.94B
91% y/y
Gross margin · GAAP
85.8%
an increase of 1.5 percentage points versus the same quarter last year y/y
EPS · non-GAAP
8.38
33% y/y
2026 full-year outlook
$85.0 billion to $87.0 billion

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
RevenueGAAP$22.97B–48%
Total Revenue, year-to-dateGAAP42,773–51%
Net income – ReportedGAAP7,095–25%
Earnings per share – ReportedGAAP7.94–26%
Net income – Non-GAAPnon-GAAP7,493–32%
Earnings per share – Non-GAAPnon-GAAP8.38–33%
Gross marginGAAP$19.7B–50%
Gross margin as a percent of revenueGAAP85.8%–an increase of 1.5 percentage points versus the same quarter last year
Research and development expensesGAAP$3.8B–14%
Research and development expenses as a percent of revenueGAAP17% of revenue––
Marketing, selling, and administrative expensesGAAP$3.4B–25%
Acquired in-process research and development chargesGAAP$2.8B––
Asset impairment, restructuring and other special chargesGAAP$703M––
Effective tax rateGAAP23.3%––
Gross marginnon-GAAP$19.8B–50%
Gross margin as a percent of revenuenon-GAAP86.3%–an increase of 1.3 percentage points versus the same quarter last year
Effective tax ratenon-GAAP22.2%––
Amortization of intangible assets per sharenon-GAAP.11––
Asset impairment, restructuring and other special charges per sharenon-GAAP.72––
Net gains on investments in equity securities per sharenon-GAAP(.39)––
Acquired IPR&D per sharenon-GAAP3.03–NM

Segments

SegmentRevenueq/qy/y
MounjaroWorldwide revenue increased primarily through volume growth. U.S. revenue reflected strong demand, partially offset by lower realized prices, while revenue outside the U.S. was driven primarily by volume growth.$9.94B–91%
ZepboundU.S. revenue increased primarily driven by strong demand, partially offset by lower realized prices, including previously announced reductions in cash-pay prices.4.93B–46%
JaypircaNo product-specific revenue driver was provided.192M–56%
EbglyssNo product-specific revenue driver was provided.201M–131%
KisunlaNo product-specific revenue driver was provided.167M–NM
OmvohNo product-specific revenue driver was provided.102M–36%
InluriyoNo product-specific revenue driver was provided.75–NM
FoundayoNo product-specific revenue driver was provided.98–NM
United States revenueA 37% increase in volume, driven by Zepbound and Mounjaro, was partially offset by a 3% decrease in realized prices.$14.4B–33%
Revenue outside the U.S.A 113% increase in volume, driven by Mounjaro, was partially offset by a 36% decrease in realized prices, primarily from Mounjaro's addition to the National Reimbursement Drug List in China.$8.6B–80%

Amounts quoted below without a unit are in millions, as in the filing’s tables. Per-share figures are as printed.

2026 full-year outlook

  • Revenue$85.0 billion to $87.0 billion
  • NoteUpdated non-GAAP EPS range of $35.50 to $36.50.
  • NoteRaised underlying non-GAAP EPS guidance for the full year by $2.78 at the midpoint, which was more than offset by $3.03 of acquired IPR&D charges from Q2 business development activity.

What drove it

  • Worldwide revenue increased 48%, driven by a 60% increase in volume, partially offset by a 13% decrease in realized prices.
  • Key Products revenue grew to $15.7 billion in Q2 2026, led by Mounjaro and Zepbound.
  • Key Products revenue in Immunology, Oncology, and Neuroscience grew 121% compared with Q2 2025.
  • Jardiance revenue outside the U.S. included a sales-based milestone of $250 million in Q2 2026 associated with the collaboration with Boehringer Ingelheim.
  • Reported gross-margin expansion was driven by improved cost of production and favorable product mix, partially offset by lower realized prices.
  • Regulatory progress included U.S. FDA approval of Ebglyss for one maintenance dose every eight weeks and European Commission approval of Jaypirca as monotherapy for adults with chronic lymphocytic leukemia across all lines of therapy.
  • The company plans to submit a Biologics License Application for retatrutide to the U.S. FDA in the first quarter of 2027.

Concerns

  • Worldwide realized prices decreased 13%, with U.S. realized prices down 3% and realized prices outside the U.S. down 36%.
  • Mounjaro's addition to the National Reimbursement Drug List in China in Q1 2026 contributed to lower realized prices outside the U.S.
  • Reported Q2 2026 results included $2.8 billion of acquired in-process research and development charges and $703 million of asset impairment, restructuring and other special charges.
  • The effective tax rate increased to 23.3% from 16.5%, primarily due to the unfavorable tax impact of non-deductible acquired IPR&D charges.
  • Marketing, selling, and administrative expenses increased 25%, primarily driven by promotional efforts supporting ongoing and planned launches.

What to watch

  • Execution against the updated 2026 full-year revenue guidance range of $85.0 billion to $87.0 billion and updated non-GAAP EPS range of $35.50 to $36.50.
  • Mounjaro and Zepbound demand, volume growth, realized-price trends, and the effects of rebates, discounts, and Zepbound cash-pay price reductions.
  • The contribution of Key Products, which grew to $15.7 billion in Q2 2026.
  • The planned first-quarter 2027 U.S. FDA Biologics License Application submission for retatrutide.
  • Integration and financial effects of the acquisitions of Orna Therapeutics, Inc., Ajax Therapeutics, Inc., Kelonia Therapeutics, Inc., and Centessa Pharmaceuticals plc.
  • Manufacturing expansion supported by the additional $4.5 billion commitment to Indiana sites.

Balance sheet and cash flow

  • Committed an additional $4.5 billion to expand Indiana manufacturing sites.

Analysis

Lilly reported a strong second quarter, with revenue of $ 22,974, up 48%, and reported EPS of 7.94, up 26%. Non-GAAP EPS increased 33% to 8.38. Worldwide growth was volume-led, as a 60% volume increase more than offset a 13% decline in realized prices. The company raised its 2026 full-year revenue guidance to $85.0 billion to $87.0 billion and updated its non-GAAP EPS range to $35.50 to $36.50.

Mounjaro and Zepbound remained the principal growth engines. Mounjaro revenue was $ 9,943, up 91%, while Zepbound revenue was 4,928, up 46%. U.S. revenue increased 33% to $14.4 billion, supported by a 37% volume increase driven by Zepbound and Mounjaro. Revenue outside the U.S. increased 80% to $8.6 billion, with Mounjaro volume growth the principal driver. Key Products revenue grew to $15.7 billion, and Key Products revenue in Immunology, Oncology, and Neuroscience grew 121% compared with Q2 2025.

Pricing is the principal counterweight to volume growth. Lower realized prices affected both geographies, particularly outside the U.S., where realized prices declined 36% primarily because Mounjaro was added to the National Reimbursement Drug List in China. In the U.S., lower realized prices reflected Zepbound and Mounjaro, although adjustments to estimated rebates and discounts partially offset the decline. Excluding these adjustments, U.S. price would have declined by approximately 9%.

Profitability remained strong at the gross-margin level. Reported gross margin increased 50% to $19.7 billion, with gross margin as a percent of revenue reaching 85.8%, an increase of 1.5 percentage points. The improvement reflected cost of production and favorable product mix, partly offset by lower realized prices. Research and development expenses increased 14% to $3.8 billion, while marketing, selling, and administrative expenses increased 25% to $3.4 billion as Lilly supported ongoing and planned launches.

Acquisition-related items materially affected reported results and the updated EPS outlook. The company recognized $2.8 billion of acquired IPR&D charges, primarily related to Orna Therapeutics, Inc. and Ajax Therapeutics, Inc., plus $703 million of asset impairment, restructuring and other special charges related to Kelonia Therapeutics, Inc. and Centessa Pharmaceuticals plc. The effective tax rate was 23.3%, compared with 16.5%, primarily due to non-deductible acquired IPR&D charges. Lilly also committed an additional $4.5 billion to expand Indiana manufacturing sites and cited regulatory, clinical, and business-development progress as it builds its pipeline and capacity.

Management, verbatim

Lilly's momentum continues, as we delivered 48% revenue growth and raised our full-year guidance.

David A. Ricks, Lilly chair and CEO

At the same time, Lilly is building for the future. With our next-generation weight-loss medicine retatrutide and its complete clinical data package in hand, new manufacturing capacity coming online, and exciting new assets entering our pipeline through business development, Lilly's future, after 150 years, has never been brighter.

David A. Ricks, Lilly chair and CEO

Not in the filing

stated, not guessed
  • Period-end date.
  • Prior-quarter comparisons for reported financial metrics.
  • GAAP operating income and operating margin.
  • Non-GAAP operating income and operating margin.
  • Operating cash flow.
  • Free cash flow.
  • Cash, cash equivalents, investments, and debt balances.
  • Share repurchases, dividends, and other capital-return amounts.
  • Full detailed 2026 guidance for gross margin, operating expenses, and tax rate.
  • Previous-release outlook needed for comparison with prior guidance.
  • Product revenue drivers for Jaypirca, Ebglyss, Kisunla, Omvoh, Inluriyo, and Foundayo.
  • Prior-year dollar amounts for gross margin, research and development expenses, and marketing, selling, and administrative expenses.

Written by an AI language model 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 checked against the filing text, and a metric whose value, prior period and change do not add up is dropped from the metrics. The model can still misread a table, in the metrics or in the text, so check a number in the filing before you rely on it. 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

SEC Form 8-K Item 2.02 with an attached earnings release (EX-99.1) covering Q2 2026 results, updated 2026 guidance, regulatory updates, and pipeline/business development highlights.

Company-level read

Ticker impact

$LLYBullishHigh confidence
Context

Lilly reported Q2 2026 revenue up 48% to $23.0B and raised full-year revenue guidance to $85.0B-$87.0B.

Expected impact

Likely positive bias for LLY on open, with follow-through dependent on how investors weigh guidance versus acquired IPR&D and realized-price pressure.

Evidence & confidence

The filing includes specific, time-sensitive updates: Q2 results, raised 2026 revenue guidance, and raised underlying non-GAAP EPS guidance, alongside quantified acquired IPR&D charges and realized price headwinds.

Market effects

Reinforces momentum in GLP-1/obesity and immunology/oncology franchises, potentially supporting sentiment across large-cap pharma weight-loss peers.

Highlights international volume growth offset by lower realized prices, including China reimbursement list dynamics.

FDA and European approvals plus obesity Phase 3 package progress can influence global pharma risk appetite for metabolic and oncology pipelines.

Counterpoint

The guidance raise is partially offset by large acquired IPR&D charges, and realized price declines (especially outside the U.S.) could cap multiple expansion if trends persist.

Key entities

  • Eli Lilly and Company

    Reported Q2 2026 financial results, raised 2026 revenue guidance, and updated pipeline and regulatory milestones.

  • retatrutide

    Phase 3 obesity program data package described as complete for global registrations, with planned U.S. BLA submission in Q1 2027.

  • Ebglyss

    U.S. FDA approval for one maintenance dose every eight weeks in moderate-to-severe atopic dermatitis.

  • Jaypirca

    European Commission approval as monotherapy for adults with chronic lymphocytic leukemia across all lines of therapy.

  • orforglipron

    U.S. submission mentioned for type 2 diabetes.

Every LLY 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.

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