STOCK TITAN

Personalis (NASDAQ: PSNL) grows MRD tests as Q1 loss widens

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Personalis, Inc. reported first quarter 2026 revenue of $15.5 million, down from $20.6 million a year earlier as non-core revenue declined while the company shifted focus to its minimal residual disease (MRD) offering. The net loss widened to $30.0 million, compared with $15.8 million in the prior-year quarter, as operating expenses increased.

Clinical test revenue rose to $1.4 million from $0.3 million, with clinical test volume surging 258% year-over-year to 7,815 tests, helped by growth in the NeXT Personal MRD test. Personalis secured Medicare coverage for lung cancer surveillance, adding to existing breast cancer coverage, and ended the quarter with about $233.2 million in cash, cash equivalents and short-term investments.

The company reaffirmed its full-year 2026 outlook, including total revenue of $78.0–$80.0 million, clinical test volume of 43,000–45,000 tests, clinical revenue of $10.0–$11.0 million, gross margin of 15%–20%, a net loss of about $105.0 million, and projected cash usage of about $100.0 million.

Positive

  • None.

Negative

  • None.

Insights

Personalis is trading near-term losses for rapid MRD-driven clinical growth.

Personalis is intentionally shifting from legacy population sequencing and enterprise sales to its NeXT Personal MRD platform. That transition drove a revenue decline to $15.5M in Q1 2026, but clinical test revenue grew to $1.4M with 7,815 tests, up 258% year-over-year.

The company secured Medicare coverage for lung cancer surveillance, adding to existing breast cancer coverage, which directly supports its MRD growth thesis. However, the strategy is expensive: net loss nearly doubled to $30.0M, and guidance for 2026 includes a net loss of about $105.0M and cash usage near $100.0M.

Personalis ended the quarter with roughly $233.2M in cash, cash equivalents and short-term investments, including $21.0M raised via an ATM program at $10.00/share. The reaffirmed revenue outlook of $78.0–$80.0M and planned five-fold clinical revenue growth indicate management’s commitment to scaling MRD despite near-term margin pressure.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Q1 2026 revenue $15.5M Three months ended March 31, 2026; vs $20.6M in 2025
Q1 2026 net loss $30.0M Three months ended March 31, 2026; vs $15.8M in 2025
Q1 2026 clinical revenue $1.4M Clinical diagnostic revenue; up from $0.3M in Q1 2025
Q1 2026 clinical tests 7,815 tests Clinical test volume; 258% year-over-year increase
Cash and investments $233.2M Cash, cash equivalents and short-term investments at March 31, 2026
2026 revenue guidance $78.0–$80.0M Full year 2026 total company revenue outlook
2026 clinical volume guidance 43,000–45,000 tests Projected full year 2026 clinical test volume
2026 net loss guidance $105.0M Projected full year 2026 net loss
minimal residual disease (MRD) medical
"the company focuses on growing revenue from its strategic MRD offering"
The presence of minimal residual disease (MRD) means a very small number of cancer cells remain in the body after treatment, too few to cause symptoms or show up on routine scans but detectable with sensitive tests. For investors it matters because MRD status is a strong early indicator of whether a patient is likely to relapse and is increasingly used as a trial endpoint and regulatory signal, affecting a therapy’s market prospects and valuation much like finding glowing embers after a fire signals risk of re-ignition.
Medicare coverage regulatory
"Received Medicare coverage approval in the first quarter for the surveillance of cancer recurrence"
Medicare coverage is the set of health insurance benefits provided by the U.S. federal Medicare program that pays for hospital care, doctor services, prescription drugs and certain medical supplies for eligible beneficiaries. Investors pay attention because changes in what Medicare will cover, how much it reimburses, or who qualifies can materially affect revenue and pricing for hospitals, drugmakers, medical device manufacturers and insurers—like rewriting the rulebook for a very large, steady customer.
neoadjuvant therapy medical
"for predicting patient outcomes following neoadjuvant therapy (NAT)"
Neoadjuvant therapy is medicine given before the main treatment—usually drugs, radiation, or both—aimed at shrinking a tumor or improving surgical outcomes. For investors it signals a strategic step in a drug’s development and commercial path: successful neoadjuvant results can make a treatment easier to use, expand its approved indications, and increase market value much like priming soil before planting improves the eventual harvest.
negative predictive value medical
"demonstrating a remarkable 100% negative predictive value and 100% specificity"
Negative predictive value is a measure of how reliable a negative result is in confirming that a person or situation is truly free of a problem or condition. For investors, it indicates the likelihood that a negative signal or indicator truly means there is no risk or issue present, helping them assess how much trust to place in avoiding potential problems based on current information.
at-the-market (ATM) sales program financial
"from the Company’s At-The-Market (ATM) sales program, executed at a weighted-average price"
An at-the-market (ATM) sales program lets a company sell newly issued shares directly into the open market at current trading prices over time through a broker, rather than selling a large block all at once. For investors, it matters because this steady, on-demand supply of new shares can dilute existing holdings and put gradual pressure on the stock price, while giving the company a flexible, cost-effective way to raise cash—like topping up a tank instead of refueling all at once.
short-term investments financial
"cash, cash equivalents, and short-term investments"
Short-term investments are financial assets purchased with the goal of turning them back into cash within about a year, including things like Treasury bills, money market funds, and short-duration bonds. They matter to investors because they provide a lower-risk, more accessible place to park money than stocks or long-term bonds—like a nearby savings box that earns some interest while staying ready for immediate needs or opportunities.
Revenue $15.5M
Net loss $30.0M
EPS basic and diluted $(0.29)
Guidance

Personalis reaffirmed 2026 guidance including revenue of $78.0–$80.0M, clinical revenue of $10.0–$11.0M, gross margin of 15%–20%, net loss of about $105.0M, and cash usage of about $100.0M.

false000152775300015277532026-05-072026-05-07

 

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): May 7, 2026

 

Personalis, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-38943

27-5411038

(State or Other Jurisdiction

of Incorporation)

(Commission

File Number)

(IRS Employer

Identification No.)

 

 

 

6600 Dumbarton Circle

Fremont, California

 

94555

(Address of Principal Executive Offices)

(Zip Code)

(650) 752-1300

Registrant’s Telephone Number, Including Area Code

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instructions A.2. below):

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

 

Trading

Symbol(s)

 

Name of each exchange on which registered

Common Stock, $0.0001 par value per share

 

PSNL

 

The Nasdaq Global Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 

 

 


 

Item 2.02 Results of Operations and Financial Condition.

On May 7, 2026, Personalis, Inc. issued a press release announcing its financial results for the quarter ended March 31, 2026. The full text of the press release is furnished as Exhibit 99.1 to this report on Form 8-K and is incorporated herein by reference.

The information in this Current Report on Form 8-K, including Exhibit 99.1, shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”), or otherwise subject to the liability of that section, and shall not be incorporated by reference into any registration statement or other document filed under the Securities Act of 1933 or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit

Number

Description

99.1

Press release of Personalis, Inc., dated May 7, 2026.

104

 

Cover Page Interactive Data File (embedded within the inline XBRL document).

 

 


 

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

Date: May 7, 2026

Personalis, Inc.

 

By:

/s/ Aaron Tachibana

Aaron Tachibana

Chief Financial Officer and Chief Operating Officer

 

 


Exhibit 99.1

 

img208356292_0.jpg

Personalis Reports First Quarter Results and Recent Highlights

Clinical test volume surged 258% year-over-year and 26% sequentially to 7,815 tests in Q1

 

Medicare coverage secured for lung cancer surveillance, providing a clear path to monetize rapidly growing clinical test volumes

FREMONT, Calif. – May 7, 2026 – Personalis, Inc. (Nasdaq: PSNL), a leader in advanced genomics for precision oncology, today reported financial and operational results for the first quarter ended March 31, 2026, highlighted recent business accomplishments, and reaffirmed financial guidance for the full year 2026.

First Quarter and Recent Strategic and Operational Highlights

Secured Milestone Medicare Coverage for Lung Cancer: Received Medicare coverage approval in the first quarter for the surveillance of cancer recurrence in lung cancer patients for Stage I to III non-small cell lung cancer (NSCLC). This marks the Company's second major coverage decision in six months, alongside breast cancer.
Announced Early Access Launch of Real-Time Variant Tracker™: Launched a pioneering new feature for NeXT Personal® that empowers clinicians to longitudinally track resistance and therapeutically targetable mutations during routine disease monitoring, and potentially optimize treatment.
Published Neoadjuvant Treatment Monitoring Results in Breast Cancer: Featured data in the Journal of Clinical Oncology from the PREDICT-DNA prospective study for Triple-Negative (TNBC) and HER2+ breast cancer patients that showed NeXT Personal can outperform current standard approaches for predicting patient outcomes following neoadjuvant therapy (NAT).

 

Presented Compelling Data at the American Association for Cancer Research (AACR) Annual Meeting:
Colorectal Cancer (CRC) Podium Presentation: Highlighted the ultrasensitive ctDNA detection by NeXT Personal for predicting and tracking response to neoadjuvant immunotherapy in CRC patients, demonstrating a remarkable 100% negative predictive value and 100% specificity for disease relapse following surgery.
Lung Cancer Poster Presentation: Demonstrated that ultrasensitive ctDNA monitoring with NeXT Personal successfully predicts the early response of immunotherapy in recurrent metastatic NSCLC patients.

First Quarter 2026 Financial Results Compared with First Quarter 2025

Quarterly Revenue: $15.5 million compared with $20.6 million; reflecting the planned decline in non-core revenue as the company focuses on growing revenue from its strategic MRD offering.
Clinical Revenue: Clinical test revenue of $1.4 million, compared with $0.3 million; delivered 7,815 clinical tests compared with 2,184, representing a 258% increase.

1

 


 

Core Revenue Streams: Pharma testing services and all other customers contributed $11.2 million. Revenue from enterprise sales (Natera) and population sequencing (the VA MVP) totaled approximately $2.9 million.
Strong Cash Position: Ended the quarter with approximately $233.2 million in cash, cash equivalents, and short-term investments. This includes approximately $21.0 million in net proceeds from the Company’s At-The-Market (ATM) sales program, executed at a weighted-average price of $10.00 per share.

CEO Commentary

"Our accomplishments in the first quarter demonstrated that our 'Win-in-MRD' strategy is working to establish NeXT Personal as the new standard for how cancer is detected and monitored," said Chris Hall, Chief Executive Officer of Personalis. " Delivering 26% sequential and 258% year-over-year clinical volume growth—especially during what is traditionally the industry's toughest seasonal quarter reflects the strong market demand for our ultrasensitive NeXT Personal test. With new Medicare coverage for lung cancer joining our existing breast cancer win, Personalis now has a reimbursement success in two of the largest oncology indications. We are transforming our ultrasensitive MRD technology from a clinical leader into a potential commercial powerhouse and we remain firmly on track to grow our clinical revenue five-fold this year.”

 

Full Year 2026 Outlook

 

Personalis reaffirmed the following guidance for the full year of 2026:

Total company revenue in the range of $78.0 to $80.0 million.
Clinical test volume scaling rapidly to a range of 43,000 to 45,000 tests, reflecting 171% growth year-over-year at the midpoint.
Clinical revenue of $10.0 to $11.0 million, representing roughly a five-fold growth year-over-year, driven by Medicare reimbursement from breast and lung cancer surveillance.
Revenue from pharma testing services and all other customers in the range of $55.0 to $56.0 million.
Revenue from population sequencing and enterprise sales of approximately $13.0 million.
Gross margin in the range of 15% to 20%, reflecting the strategic decision to accelerate clinical volume adoption ahead of full reimbursement coverage to establish market share.
Net loss of approximately $105.0 million.
Cash usage of approximately $100.0 million, driven by commercial investments to support projected clinical test volume growth and expansion.

 

About Personalis, Inc.


At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care throughout the patient journey. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable the selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. To learn more, visit www.personalis.com and connect with us on LinkedIn and X (Twitter).

 

2

 


 

Forward-Looking Statements


This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include all statements that are not historical facts and can generally be identified by terms such as “anticipate,” “estimate,” “expect,” “if,” “may,” “future,” “will” or similar expressions. These statements include statements relating to: Personalis’ full year 2026 guidance for revenue, gross margin, net loss, and cash usage, the sufficiency of Personalis’ capital to support commercial scale and execution, the expected five-fold growth in clinical revenue in 2026 and Personalis’ commercial investments supporting projected clinical test volume growth and expansion, the potential for new features of the NeXT Personal test to optimize treatment, the clinical relevance of the NeXT Personal test and the potential impact or expected benefits of the Personalis’ published data and presentations. Such forward-looking statements involve known and unknown risks and uncertainties and other factors that may cause actual results to differ materially from any anticipated results or expectations expressed or implied by such statements, including the risks, uncertainties and other factors that relate to the timing and pace of new orders from customers, including from ModernaTX, Inc., Merck Sharp & Dohme LLC and other biopharma customers, and the VA MVP; the success of Personalis’ and Tempus AI, Inc.’s respective sales and marketing efforts; the timing of tissue, blood, and other specimen sample receipts from customers, which can materially impact revenue quarter-over-quarter and year-over-year; Personalis’ ability to demonstrate attributes, advantages or clinical validity of the NeXT platform, including the NeXT Personal MRD assay remaining unique in its ability to detect traces of cancer in the ultrasensitive range; future clinical data differing from the clinical data previously presented or expected results; the rate of adoption and use of the NeXT platform, including maintaining the accelerated adoption rates experienced in 2025 and in the first quarter of 2026; Personalis’ ability to obtain Medicare coverage and reimbursement in additional indications and the timing thereof; the impact of competition and macroeconomic factors on Personalis’ business; the partnering and/or collaboration arrangements that Personalis has entered into or may enter into in the future may not be successful, or may terminate, which could adversely impact Personalis’ business or affect its ability to develop and commercialize its services and products; having a limited number of suppliers; customer concentration; and Personalis may opportunistically raise additional capital through equity offerings, debt financings, collaborations, or licensing arrangements. These and other potential risks and uncertainties that could cause actual results to differ materially from the results predicted in these forward-looking statements are described under the captions “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in Personalis’ Annual Report on Form 10-K for the year ended December 31, 2025, filed with the Securities and Exchange Commission (SEC) on February 26, 2026 and Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, to be filed with the SEC on May 7, 2026. All information provided in this release is as of the date of this press release, and any forward-looking statements contained herein are based on assumptions that we believe to be reasonable as of this date. Undue reliance should not be placed on the forward-looking statements in this press release, which are based on information available to us on the date hereof. Personalis undertakes no duty to update this information unless required by law.

 

Contacts:

Investor Relations:

Caroline Corner

investors@personalis.com

646-277-1279

Media:

pr@personalis.com

 

3

 


 

PERSONALIS, INC.

CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)

(In thousands, except share and per share data)

 

 

 

Three Months Ended March 31,

 

 

 

2026

 

 

2025

 

Revenue (1)

 

$

15,472

 

 

$

20,605

 

Costs and expenses

 

 

 

 

 

 

Cost of revenue

 

 

15,191

 

 

 

13,398

 

Research and development

 

 

14,539

 

 

 

12,640

 

Selling, general and administrative (2)

 

 

17,903

 

 

 

12,263

 

Total costs and expenses

 

 

47,633

 

 

 

38,301

 

Loss from operations

 

 

(32,161

)

 

 

(17,696

)

Interest income

 

 

2,172

 

 

 

2,027

 

Interest expense

 

 

(47

)

 

 

(28

)

Other income (expense), net

 

 

20

 

 

 

(46

)

Loss before income taxes

 

 

(30,016

)

 

 

(15,743

)

Provision for income taxes

 

 

16

 

 

 

7

 

Net loss

 

$

(30,032

)

 

$

(15,750

)

Net loss per share, basic and diluted

 

$

(0.29

)

 

$

(0.18

)

Weighted-average shares outstanding, basic and diluted

 

 

104,191,862

 

 

 

87,463,885

 

 

(1) Includes related party revenue of $3.1 million and $0.5 million for the three months ended March 31, 2026 and 2025, respectively.

(2) Includes related party sales and marketing expenses of $2.9 million and $0.6 million for the three months ended March 31, 2026 and 2025, respectively.

4

 


 

 

PERSONALIS, INC.

SUPPLEMENTAL REVENUE INFORMATION (Unaudited)

(In thousands)

 

 

 

 

 

 

 

 

Three Months Ended March 31,

 

 

 

2026

 

 

2025

 

Pharma testing services (1)

 

$

10,724

 

 

$

13,594

 

Enterprise sales

 

 

393

 

 

 

2,465

 

Population sequencing

 

 

2,500

 

 

 

4,213

 

Clinical diagnostic

 

 

1,431

 

 

 

308

 

Other

 

 

424

 

 

 

25

 

Total revenue

 

$

15,472

 

 

$

20,605

 

 

(1) Includes related party revenue of $3.1 million and $0.5 million for the three months ended March 31, 2026 and 2025, respectively.


 


 

5

 


 

 

PERSONALIS, INC.

CONSOLIDATED BALANCE SHEETS (Unaudited)

(In thousands, except share and par value data)

 

 

 

March 31, 2026

 

 

December 31, 2025

 

Assets

 

 

 

 

 

 

Current assets

 

 

 

 

 

 

Cash and cash equivalents

 

$

73,594

 

 

$

124,245

 

Short-term investments

 

 

159,624

 

 

 

115,708

 

Accounts receivable, net (1)

 

 

13,022

 

 

 

16,203

 

Inventory and other deferred costs

 

 

6,930

 

 

 

6,144

 

Prepaid expenses and other current assets

 

 

5,028

 

 

 

5,651

 

Total current assets

 

 

258,198

 

 

 

267,951

 

Property and equipment, net

 

 

48,438

 

 

 

44,815

 

Operating lease right-of-use assets

 

 

14,957

 

 

 

15,118

 

Other long-term assets

 

 

3,802

 

 

 

6,280

 

Total assets

 

$

325,395

 

 

$

334,164

 

Liabilities and Stockholders’ Equity

 

 

 

 

 

 

Current liabilities

 

 

 

 

 

 

Accounts payable (2)

 

$

12,676

 

 

$

12,989

 

Accrued and other current liabilities (2)

 

 

22,201

 

 

 

25,079

 

Contract liabilities (3)

 

 

4,168

 

 

 

1,562

 

Total current liabilities

 

 

39,045

 

 

 

39,630

 

Long-term operating lease liabilities

 

 

31,023

 

 

 

31,866

 

Other long-term liabilities

 

 

562

 

 

 

1,483

 

Total liabilities

 

 

70,630

 

 

 

72,979

 

Commitments and contingencies

 

 

 

 

 

 

Stockholders’ equity

 

 

 

 

 

 

Preferred stock, $0.0001 par value — 10,000,000 shares authorized; none issued

 

 

 

 

 

 

Common stock, $0.0001 par value — 200,000,000 shares authorized; 104,691,704 and 102,475,891 shares issued and outstanding, respectively

 

 

10

 

 

 

10

 

Additional paid-in capital

 

 

916,117

 

 

 

892,331

 

Accumulated other comprehensive income (loss)

 

 

(70

)

 

 

104

 

Accumulated deficit

 

 

(661,292

)

 

 

(631,260

)

Total stockholders’ equity

 

 

254,765

 

 

 

261,185

 

Total liabilities and stockholders’ equity

 

$

325,395

 

 

$

334,164

 

 

(1) Includes related party accounts receivable of $4.5 million and $2.5 million as of March 31, 2026 and December 31, 2025, respectively.

(2) Includes related party liabilities of $4.4 million and $5.7 million as of March 31, 2026 and December 31, 2025, respectively.

(3) Includes related party contract liabilities of $2.7 million and nil as of March 31, 2026 and December 31, 2025, respectively.

 

 

 

 

 

 

 

6

 


FAQ

How did Personalis (PSNL) perform financially in Q1 2026?

Personalis reported Q1 2026 revenue of $15.5 million, down from $20.6 million a year earlier. The company posted a net loss of $30.0 million, compared with $15.8 million in Q1 2025, as operating costs increased during its strategic shift.

How fast are Personalis (PSNL) clinical volumes and revenue growing?

Clinical test volume reached 7,815 tests in Q1 2026, a 258% year-over-year increase from 2,184 tests. Clinical revenue rose to $1.4 million from $0.3 million, reflecting rapid adoption of the NeXT Personal MRD test in oncology surveillance settings.

What Medicare coverage has Personalis (PSNL) secured for NeXT Personal?

Personalis obtained Medicare coverage in Q1 2026 for surveillance of cancer recurrence in Stage I–III NSCLC lung cancer patients. This follows an earlier coverage decision in breast cancer, giving the company reimbursement wins in two major oncology indications for its NeXT Personal MRD test.

What 2026 financial guidance did Personalis (PSNL) reaffirm?

For full-year 2026, Personalis reaffirmed total revenue guidance of $78.0–$80.0 million and clinical revenue of $10.0–$11.0 million. The company also projects a net loss of about $105.0 million and cash usage of about $100.0 million as it invests in commercial growth.

How strong is Personalis (PSNL) cash position after Q1 2026?

Personalis ended Q1 2026 with about $233.2 million in cash, cash equivalents, and short-term investments. This total includes roughly $21.0 million in net proceeds raised through an at-the-market equity program at a $10.00 per share average price.

How did Personalis (PSNL) segment revenues mix change in Q1 2026?

In Q1 2026, pharma testing services and other customers generated $11.2 million, while population sequencing and enterprise sales contributed about $2.9 million. Clinical diagnostic revenue grew to $1.4 million, highlighting a gradual shift toward MRD-focused clinical testing.

Filing Exhibits & Attachments

2 documents