Total revenue
$411.5M
Q3 2026, up 23% year over year, reported Nov. 2, 2026
First positive adjusted EPS
$0.07
Q3 2026 non-GAAP, against a $0.08 GAAP loss in the same quarter
Adjusted EBITDA
$25.6M
Q3 2026, swinging $24.1 million above the year-earlier $1.5 million
Licensing revenue (Insights)
$88.9M
Q3 2026, up 29% year over year, carrying a 72% segment gross margin
Gross profit
$266.7M
Q3 2026, up 27%, lifting gross margin to 64.8% from 62.8%
Full-year 2026 guidance
$1.60–1.605B
Raised Nov. 2, 2026, with about $65 million of adjusted EBITDA
The third quarter of 2026 is the first time healthcare AI has produced a quarter that investors can value like a software business rather than a laboratory. Tempus AI reported $411.5 million of revenue on Nov. 2, up 23% year over year, and posted its first positive adjusted earnings per share at $0.07 after an $80.0 million net loss a year earlier. The mix did the work: data and applications — the segment that licenses clinical-genomics data to drugmakers — grew 33% to $108.1 million at a 72% gross margin, and that mix lifted gross profit 27% to $266.7 million, the swing that carried adjusted EBITDA to $25.6 million from $1.5 million.
Segment economics
The 26% of revenue that carries the quarter is the part nobody prices
The licensing engine inside that number has a name: Insights, Tempus's data licensing and modeling line, and it did $88.9 million of work at a 72% gross margin. That is 21.6% of company revenue, and it grew 29% against the 20% growth of the diagnostics base it sits on top of — $303.5 million of oncology and hereditary testing that still supplies three-quarters of revenue and all of the reimbursement risk.
| Line | Q3 2026 revenue | Year over year | Share of revenue |
|---|---|---|---|
| Tempus AI total revenue | $411.5M | +23% | 100% |
| Diagnostics (oncology and hereditary testing) | $303.5M | +20% | 73.7% |
| Data and applications | $108.1M | +33% | 26.3% |
| — Insights (data licensing and modeling) | $88.9M | +29% | 21.6% |
| — NeXT (minimal residual disease) | $9.6M | +200% | 2.3% |
| — Trials (clinical trial matching) | $9.6M | +4% | 2.3% |
| Gross profit | $266.7M | +27% | 64.8% margin |
| Net loss | $(14.9)M | vs $(80.0)M | 3.6% of revenue |
| Adjusted EBITDA | $25.6M | vs $1.5M | 6.2% margin |
Where the $26.7 million of data and applications growth came from
Revenue by product line, Q3 2026 versus Q3 2025 ($ millions). Insights is licensing; NeXT is an MRD test; Trials is trial matching.
Unit: $ millions
Insights, Q3 2026
+29% year over year
88.9
Insights, Q3 2025
$19.9M of the increase
69
NeXT, Q3 2026
+200% year over year
9.6
NeXT, Q3 2025
$6.4M of the increase
3.2
Trials, Q3 2026
+4% year over year
9.6
Trials, Q3 2025
Flat
9.2
Gross margin bridge
Mix, not volume, is what closed the loss
Here is the arithmetic behind the profit. Data and applications was 24.3% of revenue a year ago and 26.3% in the quarter, so a business grossing 72% instead of 62% became two points heavier in the mix. Decomposed, the licensing segment's own 300 basis point margin gain contributed about 73 basis points of company gross margin, diagnostics contributed about 76, and the shift in mix added roughly 19.
| Driver | Change | Effect on company gross margin |
|---|---|---|
| Data and applications segment margin (72% versus 69%) | +300 bps | ≈ +73 bps |
| Diagnostics segment margin (62% versus 61%) | +140 bps | ≈ +76 bps |
| Revenue mix shift toward data and applications (24.3% to 26.3%) | +1.9 pts | ≈ +19 bps |
| Company gross margin (64.8% versus 62.8%) | +200 bps | Reported |
Gross margin by segment, Q3 2025 versus Q3 2026
The licensing segment is roughly ten points more profitable per dollar than the testing business, which is why its weight matters.
Unit: % of segment revenue
Company gross margin, Q3 2026
64.8%
Company gross margin, Q3 2025
62.8%
Data and applications, Q3 2026
+300 bps year over year
72%
Data and applications, Q3 2025
69%
Diagnostics, Q3 2026
+140 bps year over year
62%
Diagnostics, Q3 2025
61%
- Data and applications gross margin reached 72% and management targets the mid-70s for full-year 2026, which means every point of license mix adds about 10 basis points to company gross margin.
- Diagnostics gross margin rose 140 basis points to 62% even as blended oncology reimbursement slipped to about $1,700 as MRD volume grew; reimbursement excluding MRD actually improved to roughly $1,880 from $1,850, so the laboratory is getting more efficient faster than price is eroding.
- On a non-GAAP basis the same quarter shows aggregate gross margin of 66%, up 230 basis points, with data and applications at 73% and diagnostics at 64%.
Quality of earnings
The profit is made of three things investors should price, not celebrate
Now the part that decides whether this is a business or a rounding error. Tempus AI's GAAP net loss narrowed $65.1 million, to $14.9 million from $80.0 million. The operating loss narrowed just $4.1 million, to $56.9 million from $61.0 million, and the gap is a non-cash mark: $42.8 million of unrealized gains, mostly on the stake in Personalis that the company agreed to buy for $16.25 a share in July.
| Item | Q3 2026 | Comparison | Read |
|---|---|---|---|
| GAAP net loss | $(14.9)M | $(80.0)M | $65.1M of improvement |
| Unrealized gains on investments, mostly Personalis stakes | $42.8M | — | Non-cash, and removed from adjusted EBITDA |
| GAAP operating loss | $(56.9)M | $(61.0)M | $4.1M of improvement |
| Adjusted EBITDA | $25.6M | $1.5M | $24.1M of improvement |
| Stock-based compensation added back | $48.1M | $34.0M | +41%, faster than revenue |
| Contract assets (unbilled receivables) | $40.5M | $8.1M at Dec. 31, 2025 | Revenue recognized ahead of cash |
| Deferred revenue | $85.9M | $125.3M at June 30, 2026 | Contracted but unrecognized, down 31% |
| Cash provided by operating activities | $9.2M | $(7.5)M in Q2 2026 | First positive quarter |
| Cash and marketable securities | $854.4M | — | Against $1.26B of total debt |
- Stock-based compensation of $48.1 million now exceeds adjusted EBITDA of $25.6 million, and it grew 41% year over year against 23% revenue growth.
- Contract assets rose to $40.5 million from $8.1 million at the end of 2025, so licensing revenue is being recognized ahead of cash collection from biopharma customers.
- Deferred revenue fell to $85.9 million from $125.3 million three months earlier while revenue rose, meaning contracted-but-unrecognized license revenue shrank 31% sequentially; Tempus does not disclose bookings by contract length, so the size of that decline cannot be parsed further.
- Net debt is about $665 million against $854.4 million of cash and marketable securities, so the roughly $1.5 billion cash purchase of Personalis is larger than the balance sheet can fund from liquidity, and 2026 guidance assumes no contribution from it.
The incumbents
Quest and Labcorp have no such line — and January reprices theirs
This is where the print stops being a Tempus AI story. Quest Diagnostics grew third-quarter revenue 10.0% to $3.10 billion on 14.5% more requisitions while revenue per requisition fell 4.2%. Labcorp grew 6.9% to $3.81 billion, with diagnostics laboratories up just 4.4% organically and biopharma laboratory services up 9.6%. Both sell the test. Neither sells the file.
| Company | Q3 2026 revenue | Growth | Volume evidence | Gross margin |
|---|---|---|---|---|
| Tempus AI | $411.5M | +23% | Oncology tests +32% to 101,500 | 64.8% |
| Quest Diagnostics | $3,097M | +10.0% | Requisitions +14.5% | 33.6% |
| Labcorp | $3,810M | +6.9% | Diagnostics laboratories +4.4% organically | 29.1% |
Q3 2026 gross margin: the data owner versus the test vendors
Gross margin as a percentage of revenue in the September 2026 quarter.
Unit: % of revenue
Washington sets the next price. Medicare clinical lab fees took no cut in 2026, and from Jan. 1, 2027 through 2029 payment may be reduced by as much as 15% a year against the prior year's rate. The reprieve expires inside the first quarter of 2027, when both labs must reprice contracts that already yield less per requisition — and neither has a revenue line that a pharma licensing budget can substitute for.
Upstream and downstream
Who actually gets paid: a locked-up sequencer, two clouds, and drugmakers with minimum commitments
The supply chain explains why the margin gap exists. Upstream, Tempus AI buys sequencing, computing and minimal residual disease technology, then sells the output as licensed insight. Downstream, drugmakers pay for the right to train models on linked clinical, molecular and imaging records. The toll collector gets volume; the data owner gets margin.
- Illumina is Tempus's primary supplier of sequencers and laboratory reagents under a supply agreement signed in June 2021 that runs for 12 years, but it carries no minimum hardware orders, so Tempus AI could exit on 90 days' notice while Illumina carries the volume risk.
- Illumina reported third-quarter fiscal 2026 revenue of $1.13 billion, up 4.2%, raised full-year guidance to $4.64 billion to $4.66 billion, and credited healthy clinical demand and NovaSeq X placements for the beat — the substrate is growing, just far slower than Tempus's 32% oncology volume.
- Illumina and Tempus AI partnered in April 2025 to train genomic algorithms on Tempus's multimodal data, which turns a sequencer vendor into a model developer as well as a toll booth.
- Computing is bought, not owned: Tempus's annual report discloses cloud agreements with both AWS and Google, including a June 2020 multi-year Google partnership whose convertible note shrinks as Tempus procures cloud services.
- Personalis supplies the MRD engine that grew Tempus's NeXT revenue to $9.6 million from $3.2 million, and Tempus AI is buying the entire company at $16.25 a share, roughly $1.5 billion, with closing expected in late 2026 or early 2027.
- AstraZeneca is the anchor customer: a master services agreement dated Nov. 17, 2021 commits it to spend a minimum of $220 million through Dec. 31, 2026, and the minimum can rise to $320 million through 2028 at AstraZeneca's election.
- Bristol-Myers Squibb is paying up to $137.5 million over five years, about $36 million a year, to license Tempus's oncology data and models, while Pathos AI is paying $55 million over five years for Alzheimer's work; the combined agreements represent $192.5 million of cash commitments.
- Merck established a multi-year collaboration to accelerate biomarker discovery using Tempus's multimodal data and Lens, and AstraZeneca agreed to pay Tempus $35 million for foundation model work alongside a Pathos arrangement paying Tempus $200 million over three years, $50 million of it upfront.
- Tempus AI signed about $200 million of new data and applications licenses in the second quarter and booked more than $550 million of data licensing year to date, so the backlog, not the quarterly revenue, is what compounds.
| Agreement | Size | Revenue cadence |
|---|---|---|
| AstraZeneca master services agreement, Nov. 2021 | Minimum $220M through Dec. 2026 | Option to lift to $320M through 2028 |
| Bristol-Myers Squibb license of oncology data and models | Up to $137.5M over five years | About $36M a year, ratable |
| Pathos AI Alzheimer's collaboration | $55M over five years | About $11M a year |
| Combined new commitments | About $192.5M over roughly five years | Ratable |
| New data and applications licenses signed in Q2 2026 | About $200M | Recognized over contract terms |
| Data licensing bookings in 2026 to date | More than $550M | Not disclosed by contract |
That stack is the real discovery in this print. A drugmaker with roughly $50 billion of trailing revenue is paying about $36 million a year, near 0.07% of sales, for the right to train on linked clinical-genomics data. The budget is small enough to be repeatable and large enough to compound, and the holder of the data sets the price. At the Nov. 2 close of $78.48 and 182.2 million shares outstanding, Tempus AI's market value was about $14.3 billion, roughly 9.5 times its $1.51 billion of trailing revenue.
Korea
The Asian read-across: same model, no margin yet
The same business model is being attempted in Asia on a different balance sheet. Lunit, the Seoul-listed AI pathology company, reported first-quarter 2026 revenue of about 24.0 billion won, up 25% year over year, with 97% of sales from outside Korea, an operating loss narrowed 35% and an EBITDA loss narrowed 54%; first-half revenue reached 45.8 billion won, up 23%. It targets EBITDA break-even within the year and FDA clearance for its INSIGHT Risk mammography model in 2026.
- Lunit does not disclose a standalone data licensing line, so the read-across rests on the business model rather than on comparable numbers; its SCOPE revenue grew 90% year over year, which is what software and data looks like before it reaches scale.
- Its biopharma revenue is concentrated in the second half of the year, the same lumpiness that makes Tempus AI's $88.9 million licensing quarter hard to extrapolate from a single print.
- For Tempus AI the read-across is competitive rather than cooperative: a second Asian supplier of AI-on-slides data caps how fast license pricing can compound, even as it validates the category.
Catalysts and risks
Horizons: what has to happen next, and what breaks the thesis
The next two quarters are about plumbing, not narrative. The raised guide requires $458 million to $463 million of fourth-quarter revenue, about 25% growth, to land at $1.60 billion to $1.605 billion for the year with about $65 million of adjusted EBITDA — and that guidance assumes no contribution from Personalis.
| Timing | Event | Why it matters |
|---|---|---|
| Dec. 31, 2026 | Expiry of AstraZeneca's $220M minimum commitment, with an option to lift it to $320M through 2028 | The cleanest available test of whether licensing renews on the same terms |
| Late Q4 2026 to early 2027 | Personalis shareholder vote and closing at $16.25 a share, about $1.5B | Excluded from guidance; converts a mark-to-market stake into cash out the door |
| Q4 2026 | Revenue of $458M to $463M implied by full-year guidance | About 25% growth, and the first test of the raised guide |
| Jan. 1, 2027 | Medicare clinical lab fee reductions of up to 15% a year begin | First reset for Quest Diagnostics and Labcorp after the 2026 reprieve |
| 2026 to 2027 | Lunit targets FDA clearance for INSIGHT Risk and EBITDA break-even | Asia read-across on whether the model converts outside Tempus |
| 2027 | About $80M of expected reimbursement uplift from expanded xT CDx approval and tumor-only orders | Repairs a blended oncology reimbursement of about $1,700 per test |
| Q4 2026 results | First reporting period including Personalis and progress toward mid-70s data and applications gross margin | Tests whether licensing compounds through a consolidating segment |
- Over one to three years the licensing line has to get bigger, not just better: at 21.6% of revenue, each point of mix adds about 10 basis points to company gross margin, and management targets mid-70s gross margin for data and applications.
- The asset behind it is being widened. In September 2026 Tempus AI said it is building a dataset of 100,000 whole genomes linked to longitudinal clinical and imaging records for researchers and model developers, which is what makes licenses defensible in 2028 rather than 2026.
- The risks are specific. Medicare fee cuts of up to 15% a year reach Tempus AI's own test revenue from Jan. 1, 2027; Natera is the MRD incumbent with $2.71 billion of trailing revenue growing 37% in its last reported quarter; and the Personalis purchase turns a paper gain into roughly $1.5 billion of cash leaving the balance sheet.
Synthesis
What is actually proven, and the three tests that settle it
So what is proven? Not that healthcare AI is profitable: Tempus AI still lost $14.9 million on a GAAP basis and its operating loss is $56.9 million. What is proven is narrower and more useful — a licensing line worth 21.6% of revenue can grow 29% at a 72% gross margin, and that mix alone can carry a company from an $80 million quarterly net loss to positive adjusted earnings. The labs that spent two decades selling the test now face a competitor selling the file.
- If Insights growth re-accelerates above 33% while contract assets fall back toward their December level, the licensing business proves repeatable and the multiple holds.
- If data and applications gross margin reaches the mid-70s for 2026, the 200 basis point gross margin gain becomes a 300 basis point gain and the operating loss closes.
- If the fourth quarter lands at $458 million or better with adjusted EBITDA tracking to about $65 million, the first positive adjusted earnings quarter was a start rather than a peak.
The names this print actually touches
- Data and applications at 26.3% of revenue growing 33% lifts company gross margin 200 basis points to 64.8% and delivered the first positive adjusted EPS of $0.07.
- Near term, the raised guide requires $458 million to $463 million in Q4, about 25% growth, and about $65 million of full-year adjusted EBITDA.
- Over one to three years, licensing must hold a nine-point growth gap over diagnostics, 29% against 20%, to justify roughly 9.5 times trailing sales.
- Discount the quarter for quality: $41.5 million of non-cash fair-value gains, $48.1 million of stock compensation, and contract assets that rose to $40.5 million from $8.1 million.
- Requisitions rose 14.5% while revenue per requisition fell 4.2%, so Quest bought 10% growth with price and mix.
- Medicare clinical lab fees take no cut in 2026, but from Jan. 1, 2027 payment can fall by as much as 15% a year through 2029.
- Longer term, the competitor is not another lab but a data vendor: pharma budgets going to $88.9 million of licensed data do not also fund routine volume.
- Counterweight: 2026 revenue guidance was raised to $12.065 billion to $12.105 billion with adjusted EPS of $11.25 to $11.35, so the squeeze lands in 2027 estimates.
- Diagnostics laboratories grew only 4.4% organically at a 16.7% adjusted operating margin, so the fee reset lands on the slower half of a two-speed company.
- Biopharma Laboratory Services grew 9.6% organically at an 18.3% margin, but it is a services business: no line item compounds like a 72%-margin license.
- Raised guidance — revenue growth of 5.9% to 6.7% and adjusted EPS of $18.30 to $18.70 — buys time until the Jan. 1, 2027 fee schedule.
- Mixed verdict: margin expansion is real, with biopharma operating margin up 180 basis points, yet the mix still depends on test volume.
- Full-year guidance rose to $4.64 billion to $4.66 billion on Q3 revenue of $1.13 billion, up 4.2%, with management citing healthy clinical demand and NovaSeq X placements.
- Tempus's 32% oncology volume growth and 300% jump in NeXT tests pull consumables through the installed base over the next one to three years.
- Caveat: 4.2% revenue growth against Tempus's 32% test volume shows value accrues above the sequencer layer, and the 12-year supply agreement carries no minimum hardware orders.
- Q3 GAAP operating margin of 27.0% and non-GAAP EPS guidance of $5.40 to $5.45 leave room to fund the 2025 algorithm partnership with Tempus AI.
- Binary catalyst: the $16.25 a share offer, about $1.5 billion, with a shareholder vote and closing in late Q4 2026 or early 2027.
- The asset is already inside Tempus's numbers: NeXT assays produced $9.6 million of revenue in the quarter, up 200%, and drove $42.8 million of unrealized gains on the stake.
- Watch what happens after closing: whether an MRD test stays inside a segment reported at a 72% gross margin, or dilutes the mix that made the quarter work.
- Tempus's MRD volume is no longer trivial: NeXT ran about 12,000 tests in the quarter, up 300%, so a category of this size argues against treating any single vendor's franchise as unassailable.
- Natera's trailing revenue of $2.71 billion grew 37% year over year in its last reported quarter, at a 65.3% gross margin, so the incumbent is not weakening.
- Catalyst: Natera's last reported quarter was Q2 2026, so its first print with Tempus's MRD numbers public is the first direct comparison.
- Buying beats building: up to $137.5 million over five years, about $36 million a year, for oncology data licenses — roughly 0.07% of $50 billion in trailing revenue.
- Licensed multimodal data is now a budget line in oncology research, which means license pricing competes with trial data pricing and deflationary pressure builds on data vendors.
- Over one to three years, watch whether BMS expands beyond the $192.5 million committed to Tempus AI and Pathos AI; expansion validates pricing, non-expansion caps it.
- The same model without the margin: first-quarter 2026 revenue of about 24.0 billion won, up 25%, with the EBITDA loss narrowed 54% and break-even targeted in 2026.
- Catalyst: FDA clearance targeted in 2026 for INSIGHT Risk, plus biopharma revenue concentrated in the second half, which makes any single quarter unreliable.
- For Tempus AI, a second Asian supplier of AI-on-slides data caps how fast licensing prices can compound even as it validates the category.
