Tempus AI, Inc.

Tempus AI, Inc. (TEM) Market Cap

Tempus AI, Inc. has a market capitalization of $8.10B.

Price: $46.43

-5.83 (-11.16%)

Market Cap: 8.10B

NASDAQ · time unavailable

CEO: Eric Lefkofsky

Sector: Healthcare

Industry: Medical - Healthcare Information Services

IPO Date: 2024-06-14

Website: https://www.tempus.com

Tempus AI, Inc. (TEM) - Company Information

Market Cap: 8.10B|Sector: Healthcare

Company Profile

Tempus AI, Inc. operates as a healthcare technology company. It engages in providing next generation sequencing diagnostics, polymerase chain reaction profiling, molecular genotyping, and other anatomic and molecular pathology testing to healthcare providers, pharmaceutical companies, biotechnology companies, researchers, and other third parties. The company offers Insights, a license library of linked clinical, molecular, and imaging de-identified data, as well as a suite of analytical services to analytic and cloud-and-compute tools to pharmaceutical and biotechnology companies; and Trials that provides clinical trial matching services to pharmaceutical companies. In addition, it operates Next; Algos, a suite of algorithmic tests in oncology; Hub, a desktop and mobile platform for ordering, managing, and receiving tests and patient results; and Lens, a platform for researchers and scientists to find, access, and analyze Tempus data. The company has a strategic collaborations agreement with AstraZeneca and Pathos AI, Inc. to develop therapeutic programs in oncology. The company was formerly known as Tempus Labs, Inc. and changed its name to Tempus AI, Inc. in January 2023. Tempus AI, Inc. was incorporated in 2015 and is headquartered in Chicago, Illinois.

Analyst Sentiment

80%
Strong Buy

From 17 Active Polls

1Y Forecast: $73.83

▲ +59.0% Potential Upside

Consensus Target Metrics

Low Bound

$59

Median

$72

High Bound

$100

Average

$74

Price & Moving Averages

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🎯 Wall Street Analyst Intelligence Report

1-Year structural target targets, chart projections, and sentiment maps.

Average 1Y Target
$73.83
▲ +59.01% Upside
Low Target
$59.00
27% Risk
Median Target
$72.00
55% Mid
High Target
$100.00
115% Max

Consensus Trend Projection

Trailing closures vs. 12-month metrics map.

Analyst Vote Distribution

Aggregate institutional coverage sentiment weights.

Sentiment volume allocation data unavailable.

Historical valuation matrix unavailable.

⚠️

Valuation Model Suspended

API Payload Error: Inverted or negative baseline Free Cash Flow margin detected (-66.9%).

Troubleshooting Notice: The upstream financial data supplier has uploaded corrupted or inverted baseline metrics for TEM. The server sandbox cannot calculate an intrinsic value path from negative cash generation baselines.

📘 Full Research Report

ℹ️

AI-Generated Research: This report is for informational purposes only.

📘 TEMPUS AI INC CLASS A (TEM) — Investment Overview

🧩 Business Model Overview

TEMPUS AI operates at the intersection of clinical data generation and AI-enabled decision support in precision medicine, with a concentrated emphasis on oncology workflows. The business model is anchored in a vertically integrated “collect–curate–analyze–deploy” loop:

  • Collect: generate molecular and clinical information through diagnostic and related offerings, then capture pathology and structured clinical variables.
  • Curate: standardize and label data into analytics-ready assets, supporting longitudinal linkage between tumor biology, treatment history, and outcomes.
  • Analyze: apply machine learning and analytics to identify clinically relevant patterns that can inform therapeutic decisions.
  • Deploy: deliver outputs to clinicians and health systems via platform solutions and service layers that embed into real-world care processes.

This structure supports customer stickiness because clinical and operational integration increases the marginal effort required to switch vendors, while the underlying value of the dataset improves as it scales.

💰 Revenue Streams & Monetisation Model

Monetisation is primarily a blend of transactional diagnostic/testing revenue and recurring platform/service revenue. Key margin drivers include:

  • Testing and associated lab services: revenue tied to volume and test mix; margins depend on sample throughput, reagent/lab economics, and payor reimbursement.
  • Platform and software-enabled services: more recurring characteristics, with gross margin typically influenced by customer concentration, utilization, and delivery costs of analytics and data operations.
  • Clinical services and workflow enablement: monetization tied to how effectively outputs are translated into clinician-facing tools and managed services.

Over time, the combined economics are driven by the extent to which platform adoption expands within existing customers and whether additional data contributions strengthen model performance and clinical relevance.

🧠 Competitive Advantages & Market Positioning

TEMPUS’s defensibility is best described as a data gravity and switching-cost moat, reinforced by an operational footprint in oncology data workflows.

  • High switching costs (data gravity): integrations into clinical systems, standardized data pipelines, and the time required to recreate comparable datasets raise switching friction for customers (health systems, oncology practices, and research collaborations).
  • Data-scale advantage: as the curated oncology dataset grows, model training and performance can improve, supporting more compelling clinical analytics and decision support.
  • Workflow embeddedness: the value proposition depends on translating insights into usable outputs within care pathways, which creates adoption inertia.

Competitive benchmarking:

  • Foundation Medicine (genomic profiling and interpretation): strong in tumor profiling; competes on test-centric offerings with an emphasis on molecular insight, while TEMPUS’s differentiation leans more toward broader data-derived analytics and platform integration.
  • Flatiron Health (real-world data platforms in oncology): strong in oncology operational data capture; TEMPUS competes via deeper molecular/clinical dataset construction and integrated analytics delivery rather than exclusively platform infrastructure.
  • Guardant Health (liquid biopsy and molecular diagnostics): strong in circulating tumor DNA testing; TEMPUS competes by coupling molecular information with longitudinal clinical outcomes and AI-driven interpretation across care workflows.

Compared with these rivals—which may emphasize either diagnostics, profiling interpretation, or real-world data infrastructure—TEMPUS’s positioning centers on building a unified dataset and applying machine learning to generate decision support that becomes harder to replicate once embedded.

🚀 Multi-Year Growth Drivers

Over a 5–10 year horizon, growth is supported by structural demand for precision oncology and the increasing role of data-driven decision support. Primary drivers:

  • Expansion of molecular testing and digital oncology: broader adoption of genomic profiling and AI-enabled analytics across community and academic care settings.
  • Richer real-world evidence loops: healthcare systems increasingly seek evidence that ties treatment selection to outcomes, supporting demand for analytics platforms grounded in large, curated datasets.
  • Broader clinical utility of models: iterative improvements in analytics can extend usage beyond initial decision points into longitudinal monitoring, therapy selection refinement, and trial matching.
  • Network effects through data contribution: while not a classic consumer network, participation by institutions increases dataset utility, which can enhance performance and adoption by future institutions (a “business network” effect driven by data).

TAM expansion depends on penetration depth (more products per account) and the continued ability to demonstrate clinical relevance and operational efficiency that payors and providers can underwrite.

⚠ Risk Factors to Monitor

  • Regulatory and reimbursement risk: diagnostics and clinical decision-support solutions face evolving oversight requirements and payer coverage dynamics; adverse changes can pressure volumes, pricing, or adoption.
  • Data privacy and governance: healthcare data handling is subject to stringent compliance expectations; failures could constrain data partnerships and increase operational costs.
  • Technological and model-risk: AI model performance may degrade if clinical practice patterns change or if new standards for evidence emerge; maintaining validated performance is essential.
  • Competitive intensity: well-capitalized competitors with proprietary testing, datasets, or integrated workflow offerings can compress differentiation and increase customer acquisition costs.
  • Capital intensity and operating leverage: lab operations, data infrastructure, and clinical workflow enablement can require sustained investment; leverage may take longer if utilization ramps slower than expected.

📊 Valuation & Market View

The market typically values healthcare data and diagnostics/AI platforms using a blend of growth and forward monetisation capacity rather than purely current profitability. Common valuation frameworks include:

  • EV/Revenue or Price/Sales for earlier-stage or scaling profiles, where the market focuses on unit economics trajectory and recurring revenue build.
  • EV/EBITDA once operating leverage becomes measurable, contingent on sustained test volumes, platform contribution margins, and lower delivery cost per account.
  • Clinical validation milestones and reimbursement durability as qualitative “re-rating” catalysts that affect revenue visibility.

Key valuation drivers include platform adoption rates, the mix shift toward more recurring software/service revenue, evidence of durable gross margin improvements, and sustained customer expansion within oncology-heavy health system networks.

🔍 Investment Takeaway

TEMPUS AI offers a differentiated precision medicine strategy centered on curated oncology data and AI-enabled clinical decision support. The investment case rests on a data gravity/switching-cost moat that can compound as embedded customers and dataset scale improve performance and usability. The primary diligence focus should remain on regulatory durability, reimbursement economics, evidence of long-term model utility, and the pace at which recurring platform and service revenue deepens within existing clinical relationships.


⚠ AI-generated — informational only. Validate using filings before investing.

📊 AI Financial Analysis

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Earnings Data: Q Ending 2026-03-31

"TEM reported Q1’26 revenue of $348.1M and EPS of -$0.70, with net income of -$125.9M (net margin -36.2%). QoQ, revenue declined -5.2% (from $367.2M in Q4’25) while losses widened: net income moved from -$54.2M to -$125.9M (a deterioration of ~$71.7M). YoY, revenue rose +36.1% versus Q1’25 ($255.7M), but profitability weakened: net income was -$125.9M vs -$68.0M in Q1’25 (losses deepened ~+85.2%). Profitability remained under pressure across the last four quarters: gross margin improved in Q1’26 (70.998%) versus Q1’25 (60.689%), but operating margin was still deeply negative (-24.3%), and EBITDA stayed loss-making (-$84.7M). Operating cash flow was -$73.3M in Q1’26, improving versus the prior quarter’s -$218.1M, indicating less cash burn sequentially. Balance sheet resilience improved materially: cash and short-term investments totaled $639.1M at quarter-end (up from $755.0M in Q4’25) and total equity increased to $416.4M (from $491.3M in Q4’25). From a shareholder-return perspective, the stock showed strong momentum: price was $55.87 with +36.74% 1-year change, but valuation indicators imply high expectations (price-to-sales ~23.2x; dividend yield 0). Overall: improving topline, but margins and earnings quality remain the key risks."

Revenue Growth

Positive

Q1’26 revenue was $348.1M, up +36.1% YoY (+$92.4M) but down -5.2% QoQ (-$19.1M), indicating growth with some short-term softening.

Profitability

Neutral

Losses widened QoQ: net income -$125.9M vs -$54.2M (Q4’25). YoY losses also worsened: -$125.9M vs -$68.0M (+85.2% deeper loss). Operating margin remained highly negative (-24.3%), despite stronger gross margin (70.998%).

Cash Flow Quality

Caution

Operating cash flow was -$73.3M in Q1’26, which is an improvement vs -$218.1M in Q4’25, but still negative versus profitability. No dividends and no buybacks reported in the quarter.

Leverage & Balance Sheet

Fair

Liquidity is substantial with $639.1M cash & short-term investments. Total assets declined to $2.14B (from $2.27B in Q4’25) and equity fell to $416.4M (from $491.3M), while total debt remained high ($814.6M).

Shareholder Returns

Good

Price momentum was strong: +36.74% over 1 year. Dividend yield is 0% and buybacks are not evident in the provided cash flow, so total return is primarily capital appreciation.

Analyst Sentiment & Valuation

Neutral

Street targets suggest upside (consensus $83.43 vs $55.87, ~49% implied). However, valuation metrics are rich for a loss-making company (price-to-sales ~23.2x; negative P/E), increasing execution risk.

Disclaimer:This analysis is AI-generated for informational purposes only. Accuracy is not guaranteed and this does not constitute financial advice.

Fundamentals Overview

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Tempus delivered strong momentum in Q1 2026: revenue of $348.1M (+36% YoY) with Diagnostics growing nearly mid-30s percentage and Oncology unit growth around 28%. Data & applications were a standout at $87M (+40.5% YoY), led by data licensing/modeling insights (+44%) and continued bookings strength (> $100M for a third straight quarter). Management increased FY2026 guidance to $1.59B–$1.6B revenue and ~$65M adjusted EBITDA, citing improved visibility and a higher TCV trend. The key strategic driver is Insights/data durability: management highlighted large, multi-year de-identified data and modeling collaborations, including new Merck and expanded Gilead, plus ongoing strength with AstraZeneca, GSK, and BMS, suggesting “sticky” relationships scaling toward model-building. Near-term headwinds are primarily timing-based (germline lapping, regulatory feedback for xF) and MRD commercialization constrained by reimbursement and unit economics, with plans to accelerate as indications and reimbursement mature.

AI IconGrowth Catalysts

  • Oncology Diagnostics unit growth ~28% YoY, with solid tumor and liquid biopsies strong and MRD volume performing even better
  • Data & applications growth: $87M revenue (+40.5% YoY), driven by data licensing/modeling insights (+44% growth)
  • Third straight quarter of bookings >$100M; TCV improving/visibility strengthening for Data & Apps
  • xF/xT assay expansion path expected to support incremental ASP lift (management cites ~$500 incremental ASP over 1–2 years as multiple assays receive/expand FDA approvals)
  • MRD ramp constrained by reimbursement/97% tumor-informed base, with expectation of more aggressive rollout as reimbursement rounds out

Business Development

  • Merck: added in Q1 via a very large strategic data and modeling collaboration; described as comparable scale to other very large pharma strategic collaborations
  • Gilead: expanded relationship in Q1; characterized as a step-up from historic levels and part of the increasing visibility/pipeline
  • AstraZeneca: referenced as building foundation models with Tempus de-identified data
  • GSK and BMS: referenced as having very large existing collaborations
  • Alzheimer’s (multi-modal modeling): engaged to begin building a multimodal model in Alzheimer's disease; multi-million dollar project expected to finish mid-2026
  • xF FDA-related amendment: amendment to cover tumor-only cases to accelerate migration to ADLT version of the assay (decision expected imminently)

AI IconFinancial Highlights

  • Revenue: $348.1M, up a little over 36% YoY
  • Diagnostic revenue: $261.1M, almost 35% growth, driven by Oncology unit growth ~28%
  • Data revenue segment: $87M, +40.5% YoY; data licensing/modeling insights grew >44%
  • Bookings: third straight quarter with bookings north of $100M; TCV rising/visibility strongest in Data & Apps in quite some time
  • Guidance increase: FY 2026 revenue range raised to $1.59B–$1.6B; adjusted EBITDA about $65M
  • Free cash flow commentary: CFO cited Q1 OCF/FCF down ~$70M (timing of payables/bonuses and burn-down of prepayments/deferred revenue flips in Q2 expected to improve)
  • EBITDA cadence: adjusted EBITDA in Q1 referenced as negative ~$3M; management expects improvement in Q2 and back half (data margins expanding)

AI IconCapital Funding

  • No buyback amounts, debt levels, or explicit cash runway figures stated in the transcript
  • Management stated they are generating cash, remain EBITDA-positive, and 'don't need more cash' / 'don't need alternative financings' for operations

AI IconStrategy & Ops

  • FDA strategy: no new update on xF FDA submission timing; management reiterates no 2026 impact on pricing/ASPs from xF timeline
  • Solid Tumor Profiling: expanding FDA-approved assay with an amendment covering tumor-only to accelerate migration to ADLT version; decision expected imminently
  • MRD commercialization: rollout metered due to unit economics/reimbursement; sales-force scaling not yet fully unleashed to avoid loss generation
  • Oncology algorithms/attach: described 40% attach rate on Solid Tumor assays; algorithms (e.g., HRD, Tumor Origin, immune profile scoring) increasingly embedded in physician workflow

AI IconMarket Outlook

  • FY 2026 guidance: revenue $1.59B–$1.6B; adjusted EBITDA about $65M
  • MRD: rollout timing tied to reimbursement maturation; management did not provide a specific date but described incremental acceleration as reimbursement expands
  • Hereditary business: expected to return to mid-teens growth in 2H 2026 after lapping extreme prior growth (about 40%)
  • FDA decision: tumor-only/ADLT amendment decision expected 'imminently'; no update/change provided for overall xF timeline

AI IconRisks & Headwinds

  • Hereditary (germline) lapping headwind: growth slowed due to lapping extreme growth rates from a year ago; expected to normalize to mid-teens in 2H
  • MRD reimbursement constraint: limited current indications and less-rounded reimbursement profile; scaling MRD volume aggressively could create losses (management described need to meter expansion)
  • xF FDA timing uncertainty: awaiting feedback; management said it should not impact 2026 pricing/ASPs, but timing remains uncertain
  • Reimbursement-driven ASP timing uncertainty: management stated reimbursement upside is difficult to pinpoint in timing, though current volume trends remain strong
  • Industry ordering adoption uncertainty (companion diagnostics): management argued CDx label inclusion should not structurally change ordering in the U.S., but acknowledged other markets could have different dynamics

Q&A: Analyst Interest

  • Data/Insights stickiness & extension: Management said core big-data relationships are renewing at or above historical levels and added new large names—Merck in Q1 and expanded Gilead—with other late-stage discussions ongoing. They emphasized durable multi-year $100M-plus de-identified data deals and migration toward model-building with Tempus.
  • FDA/regulatory timelines & pricing/ASP durability: Management reported no update on the xF FDA submission timing and reiterated it should not affect 2026 pricing/ASP. They highlighted an ADLT acceleration amendment covering tumor-only cases with an 'imminent' decision expected; they expect increased ASPs as multiple assays become FDA-approved.
  • MRD scaling vs reimbursement constraints: Management explained MRD growth is occurring with a small dedicated sales force because reimbursement and unit economics require metering. They said ~97% of tests are tumor-informed and unloading MRD to the full sales machine prematurely would create large losses; as reimbursement rounds out, they expect more aggressive rollout.

Sentiment: POSITIVE

Note: This summary was synthesized by AI from the TEM Q1 2026 earnings transcript. Financial data is complex; please verify all metrics against official SEC filings before making investment decisions.

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