10-Q · April 30, 2026
Eli Lilly posted a robust Q1 2026 with revenues of $19.8 billion, a 56% increase from $12.7 billion in Q1 2025, and diluted EPS of $8.26, soaring 170% year-over-year. This strong performance was driven by significant…
Earnings analysis · 10-Q
Filed October 29, 2026 · Our reading of the company's report
The latest report
Lilly delivered strong year-over-year operating performance in the third quarter, with revenue up 39% to $24.397 billion, EPS up 16% to $7.22, and gross margin expanding to 83.9%. Growth was led by Mounjaro and…
Lilly delivered strong year-over-year operating performance in the third quarter, with revenue up 39% to $24.397 billion, EPS up 16% to $7.22, and gross margin expanding to 83.9%. Growth was led by Mounjaro and Zepbound, although lower realized prices, sequential EPS and gross-margin declines, and concentration in incretin products remain important offsets. Liquidity weakened as cash fell to $4.9 billion and debt rose to $49.5 billion after $18.2 billion of business-development spending; the 10-Q provides no new quantitative guidance and reports no material risk-factor changes.
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Third-quarter revenue was $24.397 billion, up 39% from $17.601 billion a year ago and approximately 6.2% above the prior-quarter revenue of $22.97 billion.
Mounjaro revenue increased 65% year over year to $10.723 billion and Zepbound revenue increased 49% to $5.352 billion. Together, the products generated $16.075 billion, or approximately 66% of quarterly revenue.
Gross margin increased to 83.9% from 82.9% in the prior year, a 1.0 percentage-point improvement, driven by improved production costs and favorable product mix despite lower realized prices.
Diluted EPS rose 16% year over year to $7.22 from $6.21, while net income increased 16% to $6.451 billion from $5.583 billion.
International revenue increased 47% to $9.261 billion, led by Mounjaro, whose outside-U.S. revenue increased 93% year over year. U.S. revenue increased 34% to $15.136 billion.
The pipeline advanced during the quarter: the FDA approved orforglipron for obesity and insulin efsitora alfa for type 2 diabetes, while Phase 3 trials for retatrutide met primary endpoints in obesity and type 2 diabetes.
Cash and cash equivalents declined to $4.9 billion from $7.3 billion at December 31, 2025, while total debt increased to $49.5 billion from $42.5 billion. The company issued $9.0 billion of long-term debt in May 2026.
Mounjaro, Zepbound, and Foundayo represented 66% of total revenue for the nine months ended September 30, 2026. Management warns that incretin volume fluctuations from channel dynamics or demand can have a disproportionate impact on results.
Revenue growth was partly offset by lower realized prices: consolidated price effects reduced the year-over-year growth rate by 15 percentage points in the quarter, including a 29-point price impact outside the U.S. Mounjaro also faced lower pricing after inclusion on China's NRDL.
Lilly paid $18.2 billion for business-development activity during the first nine months, primarily for acquisitions including Centessa and Kelonia, and acquired Merida in October for up to $2.9 billion.
The company states that Medicare beneficiaries received access to discounted Lilly obesity medicines through the Medicare GLP-1 Bridge program from July 1, 2026 through December 31, 2027, but continued uptake is unknown and could affect pricing, demand, and access.
The filing states that there were no material changes to the risk factors disclosed in the 2025 Form 10-K. Existing risks nevertheless include counterfeit, misbranded, adulterated, and mass-compounded incretins, for which Lilly states the FDA requires compounding pharmacies to cease mass production.
The 10-Q does not provide explicit quantitative revenue or EPS guidance. Management expects additional manufacturing capacity to become operational over the next several years and states that near-term performance will be affected by regulatory approvals for orforglipron and uptake in new incretin channels, including U.S. Medicare.
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