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Adaptive Biotechnologies (NASDAQ: ADPT) lifts 2026 MRD outlook after 35% Q1 revenue growth

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

Rhea-AI Filing Summary

Adaptive Biotechnologies reported strong first quarter 2026 results driven by its Minimal Residual Disease (MRD) business. Revenue was $70.9 million, up 35% from the prior-year quarter, with MRD revenue of $67.1 million, a 53% increase. Immune Medicine revenue was $3.8 million, down 57%, reflecting lower Genentech-related activity.

Net loss improved to $20.0 million from $29.8 million, and Adjusted EBITDA loss narrowed to $2.5 million from $12.7 million. The company ended March 31, 2026 with $237.2 million in cash, cash equivalents and marketable securities and raised full-year 2026 MRD revenue guidance to $260–$270 million, implying 22–27% annual growth.

Positive

  • MRD-driven growth and guidance raise: Q1 2026 revenue grew 35% to $70.9 million, with MRD revenue up 53% to $67.1 million and clonoSEQ test volume up 41%. Management raised full-year 2026 MRD revenue guidance to $260–$270 million, implying 22–27% growth.

Negative

  • Immune Medicine revenue contraction: Immune Medicine revenue fell 57% year over year to $3.8 million in Q1 2026, and segment Adjusted EBITDA loss widened to $10.4 million, highlighting ongoing weakness outside the core MRD business.

Insights

MRD growth accelerates, losses narrow, guidance raised for 2026.

Adaptive Biotechnologies posted Q1 2026 revenue of $70.9 million, up 35%, led by MRD revenue of $67.1 million growing 53%. clonoSEQ test volume rose 41% to 32,595 tests, supporting the MRD segment’s role as the main growth engine.

Immune Medicine revenue declined 57% to $3.8 million, reflecting the absence of Genentech Agreement revenue and segment pressure. Company-wide operating expenses increased 10% to $90.1 million, but net loss improved to $20.0 million and Adjusted EBITDA loss narrowed to $2.5 million, showing better operating leverage.

Cash, cash equivalents and marketable securities totaled $237.2 million as of March 31, 2026, giving the company runway to execute its strategy. Updated 2026 MRD revenue guidance of $260–$270 million, implying 22–27% growth, underscores management’s confidence in continued MRD adoption.

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 $70.9 million Quarter ended March 31, 2026; up 35% year over year
MRD revenue Q1 2026 $67.1 million 53% increase from first quarter of prior year
Immune Medicine revenue Q1 2026 $3.8 million 57% decrease from first quarter of prior year
Net loss Q1 2026 $20.0 million Improved from $29.8 million in Q1 2025
Adjusted EBITDA Q1 2026 ($2.5 million) Loss narrowed from $12.7 million loss in Q1 2025
Cash, cash equivalents and marketable securities $237.2 million As of March 31, 2026, including Digital Biotechnologies, Inc.
2026 MRD revenue guidance $260–$270 million Implied MRD revenue growth of 22–27% for full year 2026
Total operating expenses Q1 2026 $90.1 million Up 10% from $82.0 million in first quarter of prior year
Minimal Residual Disease (MRD) medical
"We apply our platform to partner with biopharmaceutical companies... across our two business segments: Minimal Residual Disease (MRD) and Immune Medicine."
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.
clonoSEQ medical
"clonoSEQ® test volume in the first quarter of 2026 increased 41% to 32,595 tests delivered versus the first quarter of 2025."
Adjusted EBITDA financial
"Adjusted EBITDA (non-GAAP) was a loss of $2.5 million for the first quarter of 2026, compared to a loss of $12.7 million for the first quarter of the prior year."
Adjusted EBITDA is a way companies measure how much money they make from their core operations, like running a business, by removing certain costs or income that aren’t part of regular business activities. It helps investors see how well a company is doing without distractions from unusual expenses or gains, making it easier to compare companies or track performance over time.
Genentech Agreement financial
"Excluding revenue recognized under the Genentech Agreement, which did not generate revenue in the quarter ended March 31, 2026, revenue for the current quarter increased 45% from the first quarter in the prior year."
revenue interest liability financial
"Revenue interest liability, net, less current portion | | | 124,749 | | | | 126,566 |"
non-GAAP financial measure financial
"this press release also includes references to Adjusted EBITDA, which is a non-GAAP financial measure that we define as net loss..."
A non-GAAP financial measure is a way companies present their financial results that excludes certain expenses or income to show how they believe their core business is performing. It matters because it can give a clearer picture of how the company is really doing, but it can also be used to make results look better than they actually are.
Revenue $70.9 million +35% YoY
MRD revenue $67.1 million +53% YoY
Immune Medicine revenue $3.8 million -57% YoY
Net loss $20.0 million improved from $29.8 million
Adjusted EBITDA ($2.5 million) improved from ($12.7 million)
Guidance

Full-year 2026 MRD revenue expected between $260 million and $270 million, implying 22–27% growth; total company operating expenses, including cost of revenue, expected between $350 million and $360 million.

0001478320False00014783202026-05-052026-05-05

 

 

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 5, 2026

ADAPTIVE BIOTECHNOLOGIES CORPORATION

(Exact name of Registrant as Specified in Its Charter)

Washington

001-38957

27-0907024

(State or Other Jurisdiction

of Incorporation)

(Commission File Number)

(IRS Employer

Identification No.)

 

 

 

1165 Eastlake Avenue East

Seattle, Washington

98109

(Address of Principal Executive Offices)

(Zip Code)

Registrant’s Telephone Number, Including Area Code: (206) 659-0067

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:

 

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, par value $0.0001 per share

 

ADPT

 

The NASDAQ Stock Market LLC

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 5, 2026, Adaptive Biotechnologies Corporation (the “Company”) issued a press release regarding the Company’s financial results for the quarter ended March 31, 2026. A copy of the press release is attached as Exhibit 99.1 and incorporated herein by reference.

The information in this Item 2.02 and the press release attached as Exhibit 99.1 hereto shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), nor shall such information be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, 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 dated May 5, 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.

 

Adaptive Biotechnologies Corporation

Date: May 5, 2026

By:

/s/ Kyle Piskel

Kyle Piskel

Chief Financial Officer

 

 


EXHIBIT 99.1

img119828894_0.jpg

Adaptive Biotechnologies Reports First Quarter 2026 Financial Results

 

 

SEATTLE, May 05, 2026 (GLOBE NEWSWIRE) – Adaptive Biotechnologies Corporation (“Adaptive Biotechnologies”) (Nasdaq: ADPT), a commercial stage biotechnology company that aims to translate the genetics of the adaptive immune system into clinical products to diagnose and treat disease, today reported financial results for the quarter ended March 31, 2026.

 

“We delivered strong first quarter results based on accelerating adoption of MRD across both clinical testing and drug development. Our performance reinforces our market leadership position and the differentiated value of our platform,” said Chad Robins, chief executive officer and co-founder of Adaptive Biotechnologies. “With disciplined execution and multiple growth drivers in place, we are well positioned to sustain our growth trajectory and create long-term value.”

Recent Highlights

Revenue for the first quarter of 2026 was $70.9 million. The MRD business, which contributed 95% of revenue, grew 53% versus the first quarter of 2025.
clonoSEQ® test volume in the first quarter of 2026 increased 41% to 32,595 tests delivered versus the first quarter of 2025.
Recognized $9.0 million in MRD pharma regulatory milestone revenue, the first U.S. primary endpoint milestone.
Raising full year 2026 MRD revenue guidance to a new range of $260 million to $270 million, implying annual growth of 22% to 27%.

First Quarter 2026 Financial Results

Revenue was $70.9 million for the quarter ended March 31, 2026, representing a 35% increase from the first quarter in the prior year. Excluding revenue recognized under the Genentech Agreement, which did not generate revenue in the quarter ended March 31, 2026, revenue for the current quarter increased 45% from the first quarter in the prior year. MRD revenue was $67.1 million for the quarter, representing a 53% increase from the first quarter in the prior year. Immune Medicine revenue was $3.8 million for the quarter, representing a 57% decrease from the first quarter in the prior year. Excluding revenue from the Genentech Agreement, Immune Medicine revenue for the quarter ended March 31, 2026 decreased 26% from the first quarter in the prior year.

Operating expenses for the first quarter of 2026 were $90.1 million, compared to $82.0 million in the first quarter of the prior year, representing an increase of 10%.

Interest and other income, net was $2.1 million for the first quarter of 2026, compared to $2.7 million in the first quarter of the prior year. Interest expense from our revenue interest purchase agreement was $2.9 million in both the first quarter of 2026 and the first quarter of the prior year.

Net loss was $20.0 million for the first quarter of 2026, compared to $29.8 million for the same period in 2025. Excluding revenue generated from the Genentech Agreement, net loss was $33.4 million for the first quarter of 2025.


Adjusted EBITDA (non-GAAP) was a loss of $2.5 million for the first quarter of 2026, compared to a loss of $12.7 million for the first quarter of the prior year. Excluding revenue generated from the Genentech Agreement, Adjusted EBITDA was a loss of $16.3 million for the first quarter of 2025.

Cash, cash equivalents and marketable securities was 237.2 million as of March 31, 2026, inclusive of $15.3 million of cash and cash equivalents held by Digital Biotechnologies, Inc.

2026 Updated Financial Guidance

Adaptive Biotechnologies expects full year revenue for the MRD business to be between $260 million and $270 million, updated from the previous range between $255 million and $265 million. No revenue guidance is provided for the Immune Medicine business.

We expect full year total company operating expenses, including cost of revenue, to be between $350 million and $360 million.

Management will provide further details on the outlook during the conference call.

Webcast and Conference Call Information

Adaptive Biotechnologies will host a conference call to discuss its first quarter 2026 financial results after market close on Tuesday, May 5, 2026 at 4:30 PM Eastern Time. The conference call can be accessed at http://investors.adaptivebiotech.com. The webcast will be archived and available for replay at least 90 days after the event.

About Adaptive Biotechnologies

Adaptive Biotechnologies (“we” or “our”) is a commercial-stage biotechnology company focused on harnessing the inherent biology of the adaptive immune system to transform the diagnosis and treatment of disease. We believe the adaptive immune system is nature’s most finely tuned diagnostic and therapeutic for most diseases, but the inability to decode it has prevented the medical community from fully leveraging its capabilities. Our proprietary immune medicine platform reveals and translates the massive genetics of the adaptive immune system with scale, precision and speed. We apply our platform to partner with biopharmaceutical companies, inform drug development, and develop clinical diagnostics across our two business segments: Minimal Residual Disease (MRD) and Immune Medicine. Our commercial products and clinical pipeline enable the diagnosis, monitoring, and treatment of diseases such as cancer and autoimmune disorders. Our goal is to develop and commercialize immune-driven clinical products tailored to each individual patient.

Forward-Looking Statements

This press release contains forward-looking statements that are based on management’s beliefs and assumptions and on information currently available to management. All statements contained in this release other than statements of historical fact are forward-looking statements, including statements regarding our ability to develop, commercialize and achieve market acceptance of our current and planned products and services, our research and development efforts and other matters regarding our business strategies, use of capital, results of operations and financial position and plans and objectives for future operations.


In some cases, you can identify forward-looking statements by the words “may,” “will,” “could,” “would,” “should,” “expect,” “intend,” “plan,” “anticipate,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “ongoing” or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. These statements involve risks, uncertainties and other factors that may cause actual results, levels of activity, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. These risks, uncertainties and other factors are described under "Risk Factors," "Management's Discussion and Analysis of Financial Condition and Results of Operations" and elsewhere in the documents we file with the Securities and Exchange Commission from time to time. We caution you that forward-looking statements are based on a combination of facts and factors currently known by us and our projections of the future, about which we cannot be certain. As a result, the forward-looking statements may not prove to be accurate. The forward-looking statements in this press release represent our views as of the date hereof. We undertake no obligation to update any forward-looking statements for any reason, except as required by law.

Use of Non-GAAP Financial Measure

To supplement our unaudited condensed consolidated statements of operations and unaudited condensed consolidated balance sheets, which are prepared in conformity with generally accepted accounting principles in the United States of America (“GAAP”), this press release also includes references to Adjusted EBITDA, which is a non-GAAP financial measure that we define as net loss attributable to Adaptive Biotechnologies Corporation adjusted for interest and other income, net, interest expense, income tax (expense) benefit, depreciation and amortization expense, impairment costs for long-lived assets, restructuring expense and share-based compensation expense. We define our segment Adjusted EBITDA in the same way to the extent the net loss attributable to Adaptive Biotechnologies Corporation and adjustments are allocable to each segment. We have provided reconciliations of net loss attributable to Adaptive Biotechnologies Corporation, the most directly comparable GAAP financial measure, to Adjusted EBITDA at the end of this press release.

Management uses Adjusted EBITDA, including segment Adjusted EBITDA, to evaluate the financial performance of our business and segments and to evaluate the effectiveness of our strategies. We present these figures because we believe it is frequently used by analysts, investors and other interested parties to evaluate companies in our industry and it facilitates comparisons on a consistent basis across reporting periods. Further, we believe it is helpful in highlighting trends in our operating results because it excludes items that are not indicative of our core operating performance.

Adjusted EBITDA, including segment Adjusted EBITDA, has limitations as an analytical tool and you should not consider it in isolation or as a substitute for analysis of our results as reported under GAAP. We may in the future incur expenses similar to the adjustments we make. In particular, we expect to incur meaningful share-based compensation expense in the future. Other limitations include that Adjusted EBITDA, including segment Adjusted EBITDA, does not reflect:

all expenditures or future requirements for capital expenditures or contractual commitments;
changes in our working capital needs;
interest expense, which is an ongoing element of our costs to operate;
income tax (expense) benefit, which may be a necessary element of our costs and ability to operate;
the costs of replacing the assets being depreciated and amortized, which will often have to be replaced in the future;
the noncash component of employee compensation expense;
long-lived assets impairment costs; and

the impact of earnings or charges resulting from matters we consider not to be reflective, on a recurring basis, of our ongoing operations, such as our restructuring activities and reductions in workforce.

 

In addition, Adjusted EBITDA, including segment Adjusted EBITDA, may not be comparable to similarly titled measures used by other companies in our industry or across different industries.

ADAPTIVE INVESTORS
Karina Calzadilla, Vice President, Investor Relations and FP&A

201-396-1687
investors@adaptivebiotech.com 

 

ADAPTIVE MEDIA
Erica Jones, Associate Corporate Communications Director

206-279-2423
media@adaptivebiotech.com 

 


 

Adaptive Biotechnologies

Condensed Consolidated Statements of Operations

(in thousands, except share and per share amounts)

(unaudited)

 

 

 

Three Months Ended March 31,

 

 

 

2026

 

 

2025

 

Revenue

 

$

70,874

 

 

$

52,443

 

Operating expenses

 

 

 

 

 

 

Cost of revenue

 

 

18,708

 

 

 

16,979

 

Research and development

 

 

23,623

 

 

 

24,203

 

Sales and marketing

 

 

26,346

 

 

 

23,047

 

General and administrative

 

 

20,984

 

 

 

17,399

 

Amortization of intangible assets

 

 

419

 

 

 

419

 

Total operating expenses

 

 

90,080

 

 

 

82,047

 

Loss from operations

 

 

(19,206

)

 

 

(29,604

)

Interest and other income, net

 

 

2,080

 

 

 

2,679

 

Interest expense

 

 

(2,889

)

 

 

(2,905

)

Net loss

 

 

(20,015

)

 

 

(29,830

)

Add: Net income attributable to noncontrolling interest

 

 

(18

)

 

 

(22

)

Net loss attributable to Adaptive Biotechnologies Corporation

 

$

(20,033

)

 

$

(29,852

)

Net loss per share attributable to Adaptive Biotechnologies Corporation common shareholders, basic and diluted

 

$

(0.13

)

 

$

(0.20

)

Weighted-average shares used in computing net loss per share attributable to Adaptive Biotechnologies Corporation common shareholders, basic and diluted

 

 

155,521,048

 

 

 

149,195,028

 

 

 


 

Adaptive Biotechnologies

Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)

 

 

 

March 31, 2026

 

 

December 31, 2025

 

 

 

(unaudited)

 

 

 

 

Assets

 

 

 

 

 

 

Current assets

 

 

 

 

 

 

Cash and cash equivalents

 

$

77,581

 

 

$

70,495

 

Short-term marketable securities (amortized cost of $140,762 and $156,246, respectively)

 

 

140,753

 

 

 

156,485

 

Accounts receivable, net

 

 

48,315

 

 

 

50,365

 

Inventory

 

 

11,206

 

 

 

9,820

 

Prepaid expenses and other current assets

 

 

13,952

 

 

 

13,020

 

Total current assets

 

 

291,807

 

 

 

300,185

 

Long-term assets

 

 

 

 

 

 

Property and equipment, net

 

 

30,774

 

 

 

34,107

 

Operating lease right-of-use assets

 

 

40,248

 

 

 

40,616

 

Long-term marketable securities (amortized cost of $18,908 and $13,220, respectively)

 

 

18,889

 

 

 

13,234

 

Restricted cash

 

 

2,709

 

 

 

2,689

 

Intangible assets, net

 

 

1,307

 

 

 

1,726

 

Goodwill

 

 

118,972

 

 

 

118,972

 

Other assets

 

 

1,237

 

 

 

1,207

 

Total assets

 

$

505,943

 

 

$

512,736

 

Liabilities and shareholders’ equity

 

 

 

 

 

 

Current liabilities

 

 

 

 

 

 

Accounts payable

 

$

9,615

 

 

$

6,467

 

Accrued liabilities

 

 

7,465

 

 

 

7,700

 

Accrued compensation and benefits

 

 

6,217

 

 

 

16,992

 

Current portion of operating lease liabilities

 

 

8,513

 

 

 

8,920

 

Current portion of deferred revenue

 

 

49,397

 

 

 

45,194

 

Current portion of revenue interest liability, net

 

 

5,804

 

 

 

4,642

 

Total current liabilities

 

 

87,011

 

 

 

89,915

 

Long-term liabilities

 

 

 

 

 

 

Operating lease liabilities, less current portion

 

 

69,115

 

 

 

70,228

 

Deferred revenue, less current portion

 

 

807

 

 

 

1,006

 

Revenue interest liability, net, less current portion

 

 

124,749

 

 

 

126,566

 

Other long-term liabilities

 

 

20

 

 

 

20

 

Total liabilities

 

 

281,702

 

 

 

287,735

 

Commitments and contingencies

 

 

 

 

 

 

Shareholders’ equity

 

 

 

 

 

 

Preferred stock: $0.0001 par value, 10,000,000 shares authorized at March 31, 2026 and December 31, 2025; no shares issued and outstanding at March 31, 2026 and December 31, 2025

 

 

 

 

 

 

Common stock: $0.0001 par value, 340,000,000 shares authorized at March 31, 2026 and December 31, 2025; 159,697,221 and 153,779,418 shares issued and outstanding at March 31, 2026 and December 31, 2025, respectively

 

 

16

 

 

 

15

 

Additional paid-in capital

 

 

1,599,708

 

 

 

1,581,848

 

Accumulated other comprehensive (loss) gain

 

 

(28

)

 

 

253

 

Accumulated deficit

 

 

(1,383,356

)

 

 

(1,363,323

)

Total Adaptive Biotechnologies Corporation shareholders’ equity

 

 

216,340

 

 

 

218,793

 

Noncontrolling interest

 

 

7,901

 

 

 

6,208

 

Total shareholders’ equity

 

 

224,241

 

 

 

225,001

 

Total liabilities and shareholders’ equity

 

$

505,943

 

 

$

512,736

 

 

 


 

Adjusted EBITDA

The following is a reconciliation of net loss attributable to Adaptive Biotechnologies Corporation, the most directly comparable GAAP financial measure, to Adjusted EBITDA for the periods presented (in thousands, unaudited):

 

 

Three Months Ended March 31,

 

 

 

2026

 

 

2025

 

Net loss attributable to Adaptive Biotechnologies Corporation

 

$

(20,033

)

 

$

(29,852

)

Interest and other income, net

 

 

(2,080

)

 

 

(2,679

)

Interest expense

 

 

2,889

 

 

 

2,905

 

Depreciation and amortization expense

 

 

3,837

 

 

 

4,731

 

Impairment of long-lived assets

 

 

347

 

 

 

 

Restructuring expense

 

 

643

 

 

 

 

Share-based compensation expense

 

 

11,928

 

 

 

12,147

 

Adjusted EBITDA

 

$

(2,469

)

 

$

(12,748

)

 

 


 

Segment Information (Including Segment Adjusted EBITDA)

The following sets forth segment information for the periods presented (in thousands, unaudited):

 

 

 

Three Months Ended March 31,

 

 

 

2026

 

 

2025

 

MRD:

 

 

 

 

 

 

Revenue

 

$

67,093

 

 

$

43,721

 

Adjusted EBITDA

 

 

12,138

 

 

 

(4,111

)

Reconciliation of Net Income (Loss) to Adjusted EBITDA:

 

 

 

 

 

 

Net income (loss)

 

$

3,362

 

 

$

(12,238

)

Depreciation and amortization expense

 

 

2,381

 

 

 

2,663

 

Impairment of long-lived assets

 

 

 

 

 

 

Restructuring expense

 

 

248

 

 

 

 

Share-based compensation expense

 

 

6,147

 

 

 

5,464

 

Adjusted EBITDA

 

$

12,138

 

 

$

(4,111

)

 

 

 

 

 

 

 

Immune Medicine(1):

 

 

 

 

 

 

Revenue

 

$

3,781

 

 

$

8,722

 

Adjusted EBITDA

 

 

(10,360

)

 

 

(5,106

)

Reconciliation of Net Loss to Adjusted EBITDA:

 

 

 

 

 

 

Net loss

 

$

(15,929

)

 

$

(10,919

)

Depreciation and amortization expense

 

 

1,005

 

 

 

1,623

 

Impairment of long-lived assets

 

 

347

 

 

 

 

Restructuring expense

 

 

395

 

 

 

 

Share-based compensation expense

 

 

3,822

 

 

 

4,190

 

Adjusted EBITDA

 

$

(10,360

)

 

$

(5,106

)

(1) Expenses related to Digital Biotechnologies, Inc. are no longer included in the Immune Medicine segment.

 


FAQ

How did Adaptive Biotechnologies (ADPT) perform financially in Q1 2026?

Adaptive Biotechnologies generated $70.9 million in Q1 2026 revenue, up 35% year over year. Net loss improved to $20.0 million from $29.8 million, and Adjusted EBITDA loss narrowed to $2.5 million, indicating better operating leverage despite higher expenses.

What drove Adaptive Biotechnologies’ revenue growth in Q1 2026?

Growth was driven by the MRD business, which delivered $67.1 million in revenue, up 53% year over year. MRD contributed 95% of total revenue, supported by a 41% increase in clonoSEQ test volume to 32,595 tests versus Q1 2025.

How did the Immune Medicine segment of ADPT perform in Q1 2026?

Immune Medicine revenue was $3.8 million in Q1 2026, a 57% decline from Q1 2025. Excluding revenue from the Genentech Agreement, segment revenue still decreased 26%, and segment Adjusted EBITDA was a loss of $10.4 million, reflecting continued softness.

What is Adaptive Biotechnologies’ updated 2026 MRD revenue guidance?

For 2026, Adaptive Biotechnologies now expects MRD revenue between $260 million and $270 million, raised from a prior range of $255–$265 million. This outlook implies annual MRD revenue growth of 22–27%, reflecting strong demand trends.

What was Adaptive Biotechnologies’ cash position as of March 31, 2026?

As of March 31, 2026, Adaptive Biotechnologies held $237.2 million in cash, cash equivalents and marketable securities. This includes $15.3 million of cash and cash equivalents at Digital Biotechnologies, Inc., supporting ongoing operations and growth initiatives.

How did Adaptive Biotechnologies’ operating expenses change in Q1 2026?

Total operating expenses were $90.1 million in Q1 2026, up 10% from $82.0 million a year earlier. Cost of revenue, research and development, sales and marketing, and general and administrative expenses all increased as the company supported expanding MRD activity.

What is Adaptive Biotechnologies’ Adjusted EBITDA trend in Q1 2026?

Adjusted EBITDA was a loss of $2.5 million in Q1 2026, compared with a loss of $12.7 million in Q1 2025. Excluding prior-year Genentech revenue, Q1 2025 Adjusted EBITDA loss was $16.3 million, highlighting substantial year-over-year improvement in underlying profitability.

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