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Adagio Medical (NASDAQ: ADGM) cuts 2025 net loss as trial enrollment ends

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

Rhea-AI Filing Summary

Adagio Medical Holdings furnished an update on fourth quarter and full year 2025 results, showing sharply lower losses driven by cost cuts and the absence of prior-year impairments. Net loss was $3.3 million for Q4 2025, down from $57.4 million in Q4 2024, and $25.1 million for 2025 versus $75.0 million in 2024.

Research and development expenses fell to $10.6 million for 2025 from $12.2 million, while selling, general and administrative expenses declined to $10.6 million from $20.0 million. Cash and cash equivalents were $17.1 million as of December 31, 2025. The company also highlighted completion of enrollment in its 209-patient -VT pivotal IDE trial for the vCLAS Cryoablation System and plans to present pivotal results at the Heart Rhythm Society conference.

Positive

  • Substantial reduction in net loss: Net loss for 2025 decreased to $25.1 million from $75.0 million in 2024, reflecting lower operating expenses and the absence of large goodwill and intangible asset impairments.
  • Meaningful operating expense cuts: Research and development expenses declined to $10.6 million from $12.2 million, and selling, general and administrative expenses dropped to $10.6 million from $20.0 million year over year.
  • Clinical milestone achieved: The company fully enrolled its 209-patient -VT pivotal IDE trial for the vCLAS Cryoablation System, with plans to present pivotal results at an upcoming Heart Rhythm Society conference.

Negative

  • Continued lack of revenue: Revenue for 2025 was reported as zero, while the company continues to incur operating and clinical development costs.
  • Ongoing losses and balance sheet pressure: Despite improvement, Adagio still recorded a $25.1 million net loss for 2025, with total liabilities of $30.9 million exceeding stockholders’ equity of $12.4 million as of December 31, 2025.

Insights

Adagio sharply reduced losses in 2025 while advancing its pivotal VT trial.

Adagio Medical remains pre-revenue in 2025 but significantly tightened its cost structure. Net loss fell to $25.1 million for 2025 from $75.0 million in 2024, helped by lower operating expenses and the absence of large goodwill and intangible impairments recorded previously.

Research and development and selling, general and administrative expenses each declined to $10.6 million for 2025, reflecting reduced headcount, fewer projects, and no SPAC-related costs. Cash and cash equivalents were $17.1 million as of December 31, 2025, with total stockholders’ equity at $12.4 million and liabilities of $30.9 million.

Strategically, the company completed enrollment of its 209-patient -VT pivotal IDE trial and plans to present results at a Heart Rhythm Society conference. Those outcomes, which will support an FDA premarket approval application for the vCLAS Cryoablation System, will be a key milestone referenced in future disclosures.

0002006986false00020069862026-03-262026-03-26

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): March 26, 2026

ADAGIO MEDICAL HOLDINGS, INC.

(Exact name of registrant as specified in its charter)

Delaware

001-42199

99-1151466

(State or other jurisdiction of incorporation)

(Commission File Number)

(I.R.S. Employer Identification No.)

26051 Merit Circle, Suite 102
Laguna Hills, CA

  ​ ​ ​

92653

(Address of principal executive offices)

  ​ ​ ​

(Zip Code)

(949) 348-1188

(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:

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

ADGM

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 or Rule 12b-2 of the Securities Exchange Act of 1934.

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 March 26, 2026, Adagio Medical Holdings, Inc. (the “Company”), issued a press release announcing the Company’s financial results for the fourth quarter and fiscal year ended December 31, 2025, and providing a business update. A copy of this press release is furnished as Exhibit 99.1 and is incorporated herein by reference.

The information furnished with this Item 2.02, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any other filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.

Item 9.01. Financial Statements and Exhibits.

(d) Exhibits.

Exhibit No.

  ​ ​ ​

Description

99.1

Press Release, dated March 26, 2026

104

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

2

SIGNATURE

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 hereunto duly authorized.

Dated: March 26, 2026

  ​ ​ ​

Adagio Medical Holdings, Inc.

 

By:

/s/ Deborah Kaster

Name:

Deborah Kaster

Title:

Chief Financial Officer and Chief Business Officer

3

Exhibit 99.1

Adagio Medical Reports Fourth Quarter and Full Year 2025 Results

LAGUNA HILLS, CA, March 26, 2026 – Adagio Medical Holdings, Inc (Nasdaq: ADGM) (“Adagio” or “the Company”), a leading innovator in catheter ablation technologies for the treatment of cardiac arrhythmias, today announced financial results for the fourth quarter ended December 31, 2025.

Fourth Quarter and Recent Business Highlights:

Announced the peer-reviewed publication in Circulation: Arrythmia and Electrophysiology, highlighting results from the U.S. Early Feasibility Study evaluating ultralow temperature cardiac ablation (“ULTA”) for the treatment of scar-related ventricular tachycardia (“VT”), which demonstrated a favorable safety profile and no device- or procedure-related major adverse events in a real-world patient cohort of both ischemic and challenging non-ischemic patients

Announced the successful completion of 13 cases with the vCLAS™ System under Expanded Access authorization from the U.S. Food and Drug Administration (“FDA”). The procedures, which included patients with premature ventricular contractions, were completed on patients who had previously failed ablations with conventional and/or experimental modalities

Appointed industry veteran Sean Salmon to the Company’s Board of Directors, enhancing strategic and governance expertise; Sean recently retired from Medtronic, Inc after a distinguished 20+ year tenure, during which he held multiple senior global leadership roles across the company’s cardiovascular and diabetes businesses

Strengthened executive leadership team with the appointments of Marie-Claude Jacques as Senior Vice President, Global Sales, and Antwan Gipson as Senior Vice President, Manufacturing & Operations, both seasoned senior executives who will help accelerate commercial readiness

Attended multiple industry and investor conferences, which involved webcasts of the corporate presentation and multiple meetings with a large spectrum of investors

Closed a private placement with gross proceeds of up to $50 million, led by a syndicate of healthcare-dedicated institutional investors; upfront proceeds of approximately $19 million expected to fund FDA submission activities and ongoing next generation catheter development, with potential for up to $31 million in additional gross proceeds upon the exercise of outstanding warrants

Completed enrollment of the 209-patient FULCRUM-VT Pivotal FDA Investigational Device Exemption (“IDE”) trial intended to support the premarket approval application for the vCLAS™  System for ablation of VT

Announced preliminary results from the FULCRUM-VT trial demonstrating 97% acute effectiveness and a favorable safety profile with the Company’s proprietary ultralow temperature technology


“2025 marked a pivotal year for Adagio as our first full year as a public company. We delivered a number of important milestones across the organization, which we believe significantly strengthen our position as we advance our ULTA technology towards commercialization,” said Todd Usen, Chief Executive Officer of Adagio. Importantly, we completed enrollment of the 209-patient FULCRUM-VT pivotal IDE trial in just eleven months, studying a real-world population of patients with both ischemic and non-ischemic cardiomyopathy, all of whom were treated with an endocardial approach. With enrollment now complete, we look forward to presenting pivotal results at the Heart Rhythm Society conference next month. As we advance toward the potential approval of vCLAS, our team is focused on preparing for commercialization while continuing to develop our next generation vCLAS technology. We remain committed to bringing our differentiated and proprietary solutions to the large and underserved population of patients living with ventricular tachycardia.”

Fourth Quarter and Full Year 2025 Financial Results

Cost of revenue was $58 thousand for the three months ended December 31, 2025, compared to $1.5 million for the three months ended December 31, 2024. Cost of revenue was $0.7 million for the full year of 2025, compared to $3.3 million for the full year of 2024. Cost of revenue decreased year-over-year due to the pause of commercial activity in Europe and the related impact of an inventory buyback conducted in connection thereto.

Research and development expenses were $2.2 million for the three months ended December 31, 2025, compared to $3.4 million for the three months ended December 31, 2024. Research and development expenses were $10.6 million for the full year of 2025, compared to $12.2 million for the full year of 2024. R&D expenses decreased year-over-year primarily due to a decrease in quality assurance costs, fewer research and development projects and reduced headcount.

Selling, general and administrative expenses were $1.7 million for the three months ended December 31, 2025, compared to $4.1 million for the three months ended December 31, 2024. Selling, general and administrative expenses were $10.6 million for the full year of 2025, compared to $20.0 million for the full year of 2024. Selling, general and administrative expenses decreased year-over year primarily due to the absence of SPAC-related corporate expenses that were incurred in 2024 and a decrease in payroll and personnel expenses related to lower headcount during the year ended December 31, 2025.

Net loss was $3.3 million for the three months ended December 31, 2025, compared to a net loss of $57.4 million for the three months ended December 31, 2024. Net loss was $25.1 million for the full year of 2025, compared to a net loss of $75.0 million for the full year of 2024. The year-over-year decrease in net loss related primarily to a $49.2 million non-cash Impairment of Goodwill and Intangibles in 2024, reduction of expenses  as well as a decrease in interest expense and the fair value revaluation of notes and warrants.

Cash and cash equivalents as of December 31, 2025 were $17.1 million.


About Adagio Medical Holdings, Inc.

Adagio is a medical device company focused on developing and commercializing products for the treatment of cardiac arrhythmias utilizing its novel, proprietary, catheter-based Ultra-Low Temperature Cardiac Ablation (ULTA) technology. ULTA is designed to create large, durable lesions extending through the depth of both diseased and healthy cardiac tissue. The Company is currently focused on the treatment of ventricular arrhythmias with its purpose-built vCLAS™ Cryoablation System, which is CE Marked and is currently under evaluation in the Company’s FULCRUM-VT U.S. Pivotal IDE Trial.

About FULCRUM VT

FULCRUM-VT (Feasibility of Ultra-Low Temperature Cryoablation in Recurring Monomorphic Ventricular Tachycardia) is a prospective, multi-center, open-label, single-arm trial, which has fully enrolled 209 patients with structural heart disease of both ischemic and non-ischemic cardiomyopathy, indicated for catheter ablation of drug refractory VT in accordance with current treatment guidelines. The results of the study will be used to apply for FDA premarket approval (PMA) for Adagio’s vCLAS™ Cryoablation System, potentially leading to the broadest industry indication for purely endocardial ablation of scar-mediated VT.

Adagio’s vCLAS™ Cryoablation System is commercially available for the treatment of monomorphic VT in Europe and select other geographies but is limited to investigational use in the United States.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “anticipates,” “believes,” “expects,” “intends,” “projects,” “plans,” and “future” or similar expressions are intended to identify forward-looking statements. Forward-looking statements include statements concerning: the potential of Adagio’s ULTA technology; the reproducibility and durability of any favorable results seen in the U.S. Early Feasibility Study and other preliminary studies; the receipt of additional gross proceeds from the private placement if the issued warrants are exercised in full; Adagio’s intended use of the proceeds from the private placement; Adagio’s strategy, future operations, future financial position, projected expenses, expected timing and results of clinical trials, prospects, plans and objectives of management; and the potential for FDA approval of Adagio’s product candidates. Forward-looking statements are based on management’s current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially and adversely from those expressed or implied by such forward-looking statements. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. Risks regarding Adagio’s business are described in detail in Adagio’s Securities and Exchange Commission (“SEC”) filings, including in its Annual Report on Form 10-K for the full-year ended December 31, 2025 and subsequent reports filed with the U.S. Securities and Exchange Commission, which are available on the SEC’s website at www.sec.gov. Additional information will be made available in other filings that Adagio makes from time to time with the SEC. These forward-looking statements speak only as of the date hereof, and Adagio disclaims any obligation to update these statements except as may be required by law.

Contact

Debbie Kaster

Chief Financial Officer and Chief Business Officer

dkaster@adagiomedical.com


Adagio Medical Holdings, Inc.

Condensed Balance Sheets

(in thousands, except share and per share data)

  ​ ​ ​

  ​ ​ ​

 

As of 
12/31/2025 

As of 
12/31/2024 

Cash and cash equivalents

$

17,105

$

20,586

Total assets

43,253

48,448

Total liabilities

30,851

28,536

Total stockholders’ equity

12,402

19,912

Condensed Statements of Operations

(in thousands, except share and per share data)

  ​ ​ ​

Year Ended December 31,

2025

2024

Successor

Successor

Predecessor

July 31 to December 31

January 1 to July 30

Revenue

$

$

269

$

333

Cost of revenue

684

1,937

1,381

Research and development

10,639

4,634

7,585

Selling, general, and administrative

10,567

6,976

13,047

Impairment – goodwill, net

30,324

Impairment - intangible assets, net

18,878

Total cost of revenue and operating expenses

21,890

62,749

22,013

Loss from operations

(21,890)

(62,480)

(21,680)

Other (expense) income:

Convertible notes fair value adjustment

(980)

929

2,059

Warrant liabilities fair value adjustment

20

6,576

191

Interest expense

(2,906)

(1,105)

(1,818)

Interest income

477

420

3

Other (expense) income, net

195

1,897

(33)

Total other (loss) income, net

(3,194)

8,717

402

Net loss

$

(25,084)

$

(53,763)

$

(21,278)

Basic net loss per share

$

(1.51)

$

(3.38)

$

(26.08)

Diluted net loss per share

$

(1.51)

$

(3.70)

$

(26.08)

Weighted-average shares outstanding – Basic

16,557,126

14,772,692

815,854

Weighted-average shares outstanding – Diluted

16,557,126

14,772,692

815,854


  ​ ​ ​

Three Months Ended December 31, 

2025

2024

Revenue

$

$

137

Cost of revenue

58

1,523

Research and development

2,235

3,417

Selling, general, and administrative

1,675

4,050

Impairment – goodwill, net

30,324

Impairment - intangible assets, net

18,878

Total cost of revenue and operating expenses

3,968

58,192

Loss from operations

(3,968)

(58,055)

Other (expense) income:

Convertible notes fair value adjustment

911

(2,326)

Warrant liabilities fair value adjustment

354

1,603

Interest expense

(775)

(670)

Interest income

132

254

Other (expense) income, net

40

1,825

Total other (loss) income, net

662

686

Net loss

$

(3,306)

$

(57,369)

Basic net loss per share

$

(0.16)

$

(3.51)

Diluted net loss per share

$

(0.21)

$

(3.62)

Weighted-average shares outstanding – Basic

20,143,796

15,204,686

Weighted-average shares outstanding – Diluted

20,143,796

15,204,686


FAQ

What were Adagio Medical (ADGM) net losses for Q4 and full year 2025?

Adagio reported a net loss of $3.3 million for Q4 2025 and $25.1 million for full year 2025. This compares to net losses of $57.4 million in Q4 2024 and $75.0 million for full year 2024, reflecting significantly lower expenses and no large impairments.

How did Adagio Medical (ADGM) operating expenses change in 2025?

Operating expenses declined meaningfully in 2025. Research and development expenses fell to $10.6 million from $12.2 million, while selling, general and administrative expenses dropped to $10.6 million from $20.0 million, driven by lower headcount, fewer projects, and no SPAC-related costs.

What is Adagio Medical’s (ADGM) cash position as of December 31, 2025?

Adagio reported cash and cash equivalents of $17.1 million as of December 31, 2025. Total assets were $43.3 million, total liabilities were $30.9 million, and stockholders’ equity stood at $12.4 million on the same date.

Did Adagio Medical (ADGM) generate revenue in 2025?

Adagio reported no revenue for the year ended December 31, 2025. In contrast, the 2024 period showed revenue figures in the financial tables, indicating the company remains focused on development rather than commercial-scale sales during 2025.

What clinical progress did Adagio Medical (ADGM) report for its vCLAS system?

Adagio completed enrollment of its 209-patient -VT pivotal IDE trial for the vCLAS Cryoablation System. The company plans to present pivotal results at a Heart Rhythm Society conference, with data intended to support an FDA premarket approval application.

What were the main reasons for Adagio Medical’s (ADGM) lower net loss in 2025?

Lower net loss in 2025 mainly reflected reduced expenses and no large impairments. The prior year included $49.2 million of non-cash goodwill and intangible impairments, as well as higher operating costs and interest-related items.

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