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Tempus AI (TEM) Q2 FY26 earnings call: guidance and Q&A

Earnings call· Jun 2026 (Q2 FY26)· Health Care· Jul 30, 2026

Source: earnings call transcript

Executive summary

Tempus AI Q2 FY26 — Strong Revenue Growth, FDA Approval, and Strategic Acquisition

Tempus AI delivered an exceptional Q2 FY26, marked by robust revenue growth driven by its Diagnostics and Data & Apps segments, alongside a strategic acquisition of Personalis to bolster its MRD testing capabilities. The company secured FDA approval for xT CDx, anticipating significant ASP uplift, and expanded its data licensing business with major pharma deals. Management raised full-year guidance, projecting continued momentum and a path to positive free cash flow by year-end, while navigating the integration of Personalis and the ramp-up of new product offerings.

Highlights

8
  • Total revenues increased 22% to $382.5 million.

  • Data and apps revenues grew 28% year-over-year to $93.2 million, with data licensing and modeling insights up 36%.

  • Received FDA approval for tumor-only xT CDx, expected to uplift ASP by $200, equating to approximately $85 million annually starting 2027.

  • Signed large multiyear data licensing and modeling agreements with BioNTech, Daiichi Sankyo, LevelSet Bio, and Insight Pharmaceuticals, contributing to approximately $200 million in total bookings.

  • Completed a $460 million convertible senior notes offering, saving over $30 million annually in interest expense and enabling positive free cash flow by year-end.

  • Adjusted EBITDA improved by $13.6 million year-over-year to $8 million.

  • Acquired Personalis to accelerate MRD testing commercial adoption, a $20 billion+ market.

  • Increased full-year 2026 revenue guidance to $1.595 billion-$1.605 billion (25% growth) and adjusted EBITDA guidance to $65 million ($72 million improvement over 2025).

Concerns

1
  • Slower growth in hereditary cancer testing, up 5% to $107.4 million, due to lapping an abnormally high growth period in Q2 2025.

Guidance & targets

CategoryTargetConfidence
Full-year 2026 Revenue
$1.595 billion to $1.605 billion
high materiality
High
Full-year 2026 Adjusted EBITDA
approximately $65 million
high materiality
High
Annual Revenue Uplift
approximately $85 million
medium materiality
High
Incremental ASP lift
additional $550
medium materiality
High
Total Revenue Uplift
approximately $400 million
high materiality
High
Free Cash Flow
positive
high materiality
High
Adjusted EBITDA and Free Cash Flow
continued improvement
medium materiality
High
Data business growth rate
close to 30% range plus or minus
high materiality
High
Hereditary growth rates
mid-teens growth
medium materiality
Medium
xF ADLT price
$7,500
medium materiality
High

Segment performance

SegmentRevenueYoYQoQMargin
Diagnostics
Slower growth in hereditary cancer testing was offset by higher growth in CGP testing due to acceleration in the business. Hereditary revenue growth was impacted by lapping an abnormally high growth period in Q2 2025.
Hereditary revenue: $107.4 millionHereditary growth: 5% YoYCGP testing growth: higher (offsetting hereditary)MRD tests in Q2: approximately 9,000MRD tests in Q1: approximately 6,500MRD QoQ growth: 38%
$289.3 million20%——
Data and Apps
Strong growth driven by data licensing and modeling business insights.
Data licensing and modeling business insights growth: 36%
$93.2 million28%——

TEM operating KPIs by quarter

TEM operating KPIs stated on its earnings calls, by fiscal quarter
KPI Dec 2025 Q4 FY25 Mar 2026 Q1 FY26This call Jun 2026 Q2 FY26Change vs prior quarter
Average selling price (ASP) Diagnostics
~$1,640 And then in response to the ASP question, so ASPs in Q4 were around $1,640. Source: earnings call transcript
~$1,740 I do -- we do believe that ASPs are likely to rise years by virtue back that our current ASP sits at around 1740 or something like that, somewhere in that range, 720. Source: earnings call transcript
——
Procedures MRD
4,700 We were simply highlighting the really unbelievable strength of our MRD offering on -- the main vector being we ran 4,700 tests. Source: earnings call transcript
6,500 I mean our MRD assay grew 500%, but it was only 6,500 a test. Source: earnings call transcript
~9,000 Even with that, we are delivering growth rates that have exceeded our expectations, running approximately 6,500 tests in Q1 and approximately 9,000 tests in Q2, growing 38% quarter-over-quarter. Source: earnings call transcript
—

Operating figures the company stated on at least two of the calls shown, checked against each call's transcript. Click a figure to read the sentence. A dash means it was not stated that quarter.

Product announcements

ProductTypeDetails
tumor-only xT CDxlaunch
GenomeNextlaunch

Deals & partnerships

BioNTech Large multiyear data licensing and modeling agreement. multiyear

BioNTech joins AstraZeneca, GlaxoSmithKline, Bristol Myers Squibb, and Merck as a key pharma partner.

Daiichi Sankyo Large data licensing and modeling agreement.
LevelSet Bio Large data licensing and modeling agreement.
Insight Pharmaceuticals Large data licensing and modeling agreement.
Personalis Agreement to acquire Personalis, a minimal residual disease (MRD) testing company.

Transaction structured as 100% stock with Tempus having option to elect payment in cash capped at 50% of consideration. Intention to finance large portion with debt to minimize shareholder dilution.

Ares Capital Repayment of outstanding loan.

Repaid using proceeds from $460 million convertible senior notes offering.

Risks & headwinds

Slower growth in hereditary cancer testing Q2 FY26

5% YoY growth in Q2 FY26, compared to abnormally high growth in Q2 FY25.

Mitigation:Offset by higher growth in CGP testing; management aims for mid-teens hereditary growth by year-end.

Personalis acquisition termination risk due to stock price Near-term, until deal closes.

Shares trading below $46 (analyst's observation).

Mitigation:Management believes Personalis strongly desires the deal to close; Tempus has the option to use cash for up to 50% of the consideration to minimize dilution, and intends to use debt financing.

What to watch in Q3 FY26

Personalis ASP improvement

2027
Current Early on the ASP curve, with first couple of indications approved.
Target Continued improvement as additional indications secure coverage.

Why it matters

Improved ASPs are crucial for Personalis' profitability and for Tempus to ramp up MRD sales force without negative margins.

On ASP, obviously, they've gotten coverage in several indications over the last several quarters. And so there's been improvement on the Personalis front. They have more indications that are coming down the pipeline as well. And so over time, obviously, we would anticipate ASPs to continue to improve as they secure coverage and additional indications.

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Q&A highlights

Seeking clarity on Personalis' ASP improvement trajectory and how incremental MRD data will enhance Tempus' data offering for biopharma clients.

Management explained that Personalis' ASPs are expected to improve with additional indications securing coverage, and volumes will increase by expanding the sales force. Eric highlighted that MRD data is becoming crucial for biopharma clients to understand study endpoints and patient recurrence earlier than traditional scans, making it a compelling component of their data offering.

“Almost every major biopharma client we have that's running large studies is trying to understand the endpoint of those studies... And more and more, you're getting earlier signals from these kind of MRD tests that are showing signs of cancer recurring 6 months or 12 months before a scan.”

asked by Kallum Titchmarsh · answered by James Rogers, Eric Lefkofsky

2 min read 6 chapters

Detailed narrative

Q2 FY26 Performance Overview

Tempus reported a strong second quarter with total revenues increasing 22% year-over-year to $382.5 million. This marks the first quarter fully integrating Ambry's results. The Diagnostics business contributed $289.3 million, up 20%, driven by accelerated CGP testing growth offsetting slower hereditary cancer testing. Data and Apps revenue grew 28% to $93.2 million, with data licensing and modeling insights up 36%.

Strategic FDA Approvals and Pipeline

The company received FDA approval for tumor-only xT CDx, enabling migration of its solid tumor DNA portfolio to unified ADLT pricing. This is projected to yield an estimated $200 ASP uplift, translating to approximately $85 million annually starting 2027. Furthermore, the liquid biopsy, xF, is currently under FDA review, with an anticipated approval in late 2027, expected to provide an additional $550 incremental ASP lift.

The combined impact of xT CDx and xF approvals is projected to generate approximately $400 million in revenue uplift by 2028.

Advancements in AI and Data Licensing

Tempus successfully delivered the first version of its foundation model to AstraZeneca, which demonstrated predictive capabilities for patient response in clinical trials. This milestone underscores the company's AI leadership. The data licensing business saw significant expansion with new multiyear agreements signed with BioNTech, Daiichi Sankyo, LevelSet Bio, and Insight Pharmaceuticals, contributing to $200 million in total bookings this quarter.

These deals, following Merck last quarter, highlight the increasing instrumental role of Tempus' data and modeling capabilities for pharmaceutical partners.

Financial Strengthening and Capital Allocation

Tempus completed a $460 million offering of 0.0% convertible senior notes due 2032, using proceeds to repay an Ares Capital loan. This transaction is expected to save over $30 million annually in interest expense, positioning the company to achieve positive free cash flow by year-end.

The company ended the quarter with a strong cash position of $820.7 million, up from $643.8 million last quarter, and significantly improved cash used in operating activities to negative $7.5 million.

Personalis Acquisition and MRD Market

Tempus announced the acquisition of Personalis, aiming to accelerate its commercial adoption of minimal residual disease (MRD) testing, a market estimated at over $20 billion. The acquisition is structured as a stock transaction with an option for up to 50% cash, with Tempus intending to finance a large portion with debt to minimize dilution.

Despite the acquisition, Tempus expects continued improvement in adjusted EBITDA and free cash flow in 2027. MRD test volumes grew 38% quarter-over-quarter, reaching approximately 9,000 tests in Q2, even with only 10% of the sales force currently selling the product.

GenomeNext Launch and Rare Disease Outlook

The launch of GenomeNext, a whole genome sequencing product, has shown promising early results, exceeding initial expectations by 50% in its first month. While currently small in volume, it is not cannibalizing the whole exome business. Management is cautiously optimistic about its contribution to hereditary growth rates, aiming for mid-teens growth by year-end, but notes that the oncology testing and data businesses are currently overperforming.

Summary of the company's earnings call; see how call summaries are prepared. Not investment advice.