10-Q · April 28, 2026
Incyte reported Q1 2026 revenue of $1,273,000,000 and diluted EPS of $1.81, both beating consensus (revenue est. $1,218,892,208; EPS est. $1.31). Revenue is up ~21% versus Q1 2025 ($1.05B) but down versus the prior…
Earnings analysis · 10-Q
Filed July 28, 2026 · Our reading of the company's report
The latest report
Incyte delivered strong Q2 results, with revenue of $1.674 billion and diluted EPS of $2.81, supported by broad product growth and a $246.0 million one-time OPZELURA CMS settlement benefit. Excluding that benefit,…
Incyte delivered strong Q2 results, with revenue of $1.674 billion and diluted EPS of $2.81, supported by broad product growth and a $246.0 million one-time OPZELURA CMS settlement benefit. Excluding that benefit, revenue growth remains healthy, led by JAKAFI demand and rapid expansion in ZYNYZ, NIKTIMVO and MONJUVI/MINJUVI. Cash generation was robust, but the subsequent $1.25 billion Vega acquisition, ongoing R&D investment, JAKAFI's 2028 exclusivity expiry and drug-pricing exposure temper the otherwise positive operating trajectory.
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Where each $100 of revenue went in this report.
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The business segments reported by the company.
Shares of the segments disclosed in this filing, largest first.
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Q2 revenue rose 37.7% year over year to $1.674 billion from $1.216 billion and approximately 31.8% sequentially from $1.27 billion in Q1 2026. The reported total includes a $246.0 million one-time, non-cash OPZELURA benefit from the CMS settlement; excluding it, revenue was approximately $1.428 billion, up 17.5% year over year.
GAAP diluted EPS increased 37.7% year over year to $2.81 from $2.04, while net income rose to $585.6 million from $405.0 million. EPS also increased 91.2% sequentially from $1.47 in Q1 2026.
Calculated gross margin expanded to 93.7% from 93.5% a year earlier and 91.8% in Q1 2026. Calculated operating margin was 41.7%, up from 23.7% sequentially but below 43.6% in Q2 2025, which benefited from a $242.2 million contract-dispute settlement gain.
Core franchise growth remained broad: JAKAFI/JAKAFI XR sales rose $52.9 million year over year to $816.7 million, with paid demand up 9%; excluding the CMS item, OPZELURA grew $39.2 million to about $203.7 million, driven by $48.2 million of volume growth partly offset by a $9.0 million price decline.
Newer hematology/oncology products grew rapidly year over year: ZYNYZ increased to $49.9 million from $8.9 million, NIKTIMVO to $60.3 million from $36.2 million, and MONJUVI/MINJUVI to $53.7 million from $31.1 million. Product royalty revenue also increased to $174.7 million from $151.1 million, led by JAKAVI royalties of $124.2 million.
Six-month operating cash flow rose to $877.0 million from $310.8 million, while capital expenditures were only $22.6 million, implying approximately $854.4 million of six-month free cash flow and 2.6% capex intensity. Liquidity was $4.5 billion at June 30, with no revolver borrowings; subsequent $1.25 billion cash consideration for Vega reduces pro forma liquidity to roughly $3.25 billion before subsequent cash generation.
Reported OPZELURA sales of $449.7 million include a $246.0 million one-time, non-cash reversal of prior CMS-related accruals. Excluding this item, quarterly OPZELURA sales were approximately $203.7 million, making the reported 173.4% year-over-year increase non-recurring in large part.
The company paid $1.25 billion in July 2026 to acquire Vega Therapeutics, following June 30 liquidity of $4.5 billion. Management identifies integration, development, commercial execution, potential write-offs and contingent liabilities as acquisition risks; latarcibart VIVID-6 topline data are not anticipated until early 2029.
JAKAFI/JAKAFI XR remained the largest product at $816.7 million, or 48.8% of total $1.674 billion revenue, and management expects JAKAFI sales to begin declining after patent exclusivity expires in 2028. Generic litigation remains pending against certain manufacturers, despite settlements with several challengers.
The filing newly emphasizes government pricing-policy exposure, including a May 12, 2025 executive order directing HHS to establish most-favored-nation price targets. It also notes that the Medicaid rebate cap was eliminated effective January 2024 and that government rebates/chargebacks may rise with price increases above inflation.
R&D expense increased 4.5% year over year to $517.0 million as clinical research and outside services reached $292.2 million. Management expects significant continuing development investment, while future Q3 Vega-related IPR&D expense was not quantified in this 10-Q.
The 10-Q does not provide numerical full-year revenue or EPS guidance. MD&A contains pipeline timing expectations, including potential U.S. tafasitamab and povorcitinib approvals in Q1 2027, and expects improved OPZELURA gross-to-net following the CMS resolution.
Incyte reported Q1 2026 revenue of $1,273,000,000 and diluted EPS of $1.81, both beating consensus (revenue est. $1,218,892,208; EPS est. $1.31). Revenue is up ~21% versus Q1 2025 ($1.05B) but down versus the prior…
Incyte’s 10-K highlights continued revenue scale driven by product sales (Q4 revenue $1,179,000,000; implied FY 2024 revenue $4,241,630,000 using quarterly results). The company shows very high product gross margins…
Incyte reported Q3 revenues of $1,137,871,000, up $218,846,000 (23.8%) versus Q3 2023, driven by product and royalty growth. Operating income declined to $146,085,000 from $214,705,000 a year ago (operating margin…
Incyte reported Q2 revenue of $1,043,759,000, up $89,149,000 (+9.3%) versus Q2 2023, but posted a large operating loss of $478,130,000 and net loss of $444,601,000 (diluted EPS $(2.04)). Cash and cash equivalents fell…
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