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Lifecore Biomedical Q3 net loss widens to $40.1M

Three development-phase programs were secured early in the fourth quarter, while quarter-end liquidity was approximately $38.0 million.

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Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

Form Type
8-K

Rhea-AI Filing Summary

Lifecore Biomedical, Inc. (LFCR) reported third-quarter 2026 revenue of $25.3 million, down 18.6% from $31.1 million a year earlier, and a net loss of $40.1 million versus $10.0 million. Gross profit was $6.8 million, compared with $7.8 million. The company recorded a $31.270 million loss from the change in fair value of its related-party debt derivative liability, versus $0.375 million a year earlier. Adjusted EBITDA, a non-GAAP measure, increased to $4.0 million from $3.1 million.

For the first nine months, revenue was $82.7 million, down 21.8%, and net loss was $61.2 million versus $20.9 million; Adjusted EBITDA was $13.6 million versus $21.1 million. Operating cash flow was $9.5 million and free cash flow was $6.914 million. Quarter-end liquidity was approximately $38.0 million, including $23.0 million in cash and $15.0 million in revolving credit availability. Lifecore secured two technology-transfer projects in the quarter and three development-phase programs early in the fourth quarter, including one Phase 2 and two Phase 3 products. It expects the two technology-transfer projects to contribute to long-term revenue growth objectives beginning in 2027.

2 points · 0 major

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It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

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1 major · 5 points

How the balance works

Positive

  • Moderate pointThird-quarter Adjusted EBITDA increased $1.0 million to $4.0 million.
  • Moderate pointNine-month free cash flow was $6.914 million, versus $2.714 million.

Negative

  • Major pointThird-quarter net loss reached $40.1 million, versus $10.0 million.
  • Moderate pointThird-quarter revenue declined 18.6% to $25.3 million year over year.
  • Moderate pointNine-month Adjusted EBITDA fell $7.4 million to $13.6 million.
  • Moderate pointNine-month operating cash flow declined to $9.457 million from $12.506 million.
  • Minor pointNine-month revenue declined 21.8% to $82.7 million year over year.
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, or exhibit attachments filed with this report.
Third-quarter revenue $25.3 million Three months ended September 30, 2026; $31.1 million in 2025
Nine-month revenue $82.7 million Nine months ended September 30, 2026; $105.7 million in 2025
Third-quarter net loss $40.1 million Three months ended September 30, 2026; $10.0 million in 2025
Third-quarter gross profit $6.8 million Three months ended September 30, 2026; $7.8 million in 2025
Third-quarter Adjusted EBITDA $4.0 million Three months ended September 30, 2026; $3.1 million in 2025
Nine-month Adjusted EBITDA $13.6 million Nine months ended September 30, 2026; $21.1 million in 2025
Nine-month free cash flow $6.914 million Nine months ended September 30, 2026; $2.714 million in 2025
Quarter-end liquidity Approximately $38.0 million At the end of the third quarter of 2026; includes $23.0 million cash and $15.0 million revolving credit availability
contract development and manufacturing organization (CDMO) technical
"fully integrated injectables contract development and manufacturing organization"
A contract development and manufacturing organization (CDMO) is a company that develops and produces drugs, vaccines or other medical products for other firms, handling steps from formulation and testing to large-scale manufacturing and quality control. Investors care because CDMOs function like outsourced specialized factories and development partners: their revenue grows when many clients need production capacity or development expertise, so their performance signals broader industry demand and is tied to regulatory approvals and client programs.
process performance qualification (PPQ) technical
"process performance qualification (PPQ) batches"
Process Performance Qualification (PPQ) is the formal test that proves a manufacturing process can consistently produce a safe, high-quality product at commercial scale. Think of it like a final dress rehearsal where the factory runs full production several times to show the results meet required standards; for investors, successful PPQ reduces regulatory and supply risk, supports reliable sales, and signals that production-related costs and timelines are predictable.
Adjusted EBITDA financial
"Adjusted EBITDA and free cash flow are non-GAAP measures"
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.
free cash flow financial
"Free cash flow is a non-GAAP financial measure"
Free cash flow is the amount of money a company has left over after paying all its expenses and investing in its business, like buying equipment or updating facilities. It shows how much cash is available to reward shareholders, pay down debt, or save for future growth. This helps investors understand if a company is financially healthy and able to grow.
debt derivative liability financial
"change in fair value of debt derivative liability, related party"
Third-quarter revenue $25.3 million decreased 18.6% from $31.1 million in the prior-year quarter
Third-quarter net loss $40.1 million compared with $10.0 million in the prior-year quarter
Third-quarter Adjusted EBITDA $4.0 million increased $1.0 million from $3.1 million in the prior-year quarter
Nine-month revenue $82.7 million decreased $23.0 million, or 21.8%, from $105.7 million

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What were LFCR's third-quarter 2026 revenue and net loss?

Lifecore reported revenue of $25.3 million, down 18.6% from $31.1 million, and a net loss of $40.1 million compared with $10.0 million in the prior-year quarter.

How much liquidity did LFCR report at September 30, 2026?

Lifecore reported approximately $38.0 million in liquidity, including $23.0 million in cash and $15.0 million of revolving credit availability.

What new programs did LFCR secure?

Lifecore secured two technology-transfer projects during the third quarter: one supporting process performance qualification batches for a biotech company's new drug application for a new chemical entity, and one supporting a marketed product for a large pharmaceutical company. Early in the fourth quarter, it secured three development-phase programs: one Phase 2 product and two Phase 3 products.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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FALSE000100528600010052862026-08-052026-08-05

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): November 4, 2026
LIFECORE BIOMEDICAL, INC.
(Exact name of registrant as specified in its charter)
Delaware
000-2744694-3025618
(State or other jurisdiction of incorporation)
(Commission file number)(IRS Employer Identification No.)
   3515 Lyman Boulevard
 Chaska,
Minnesota
55318
(Address of principal executive offices)(Zip Code)
(952) 368-4300
(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 communication 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 classTrading SymbolName of each exchange on which registered
Common stock, par value $0.001 per shareLFCRThe NASDAQ Global Select 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 November 4, 2026, Lifecore Biomedical, Inc. (the “Company”) issued a press release announcing its consolidated financial results for the third quarter and nine months ended September 30, 2026. The press release is furnished herewith as Exhibit 99.1.
The information in this Item 2.02 of this Current Report, including Exhibit 99.1, is being furnished and 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. The information in this Item 2.02 of this Current Report, including Exhibit 99.1, shall not be 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 a filing.
Item 9.01    Financial Statements and Exhibits.
(d) Exhibits
Exhibit No.Description
99.1
Press Release issued November 4, 2026 by Lifecore Biomedical, Inc.
104Cover Page Interactive Data File - the cover page XBRL tags are embedded within the Inline XBRL document.



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.
Date: November 4, 2026
LIFECORE BIOMEDICAL, INC.
By:/s/ Ryan D. Lake
Ryan D. Lake
Chief Financial Officer

Exhibit 99.1
Lifecore Biomedical Reports Financial Results for the Third Quarter Ended September 30, 2026, and Provides Corporate Update
-- Multiple New Business Wins Continue to Strengthen Growing Pipeline --
CHASKA, Minn., November 4, 2026 -- Lifecore Biomedical, Inc. (NASDAQ: LFCR) (“Lifecore”), a fully integrated injectables contract development and manufacturing organization (“CDMO”), today announced results for the third quarter and nine months ended September 30, 2026.
CEO Commentary
“During the third quarter, Lifecore secured two new technology transfer projects. One will support process performance qualification (PPQ) batches for a biotech company’s new drug application (NDA) for a new chemical entity, and the other will support a currently marketed product for a large pharmaceutical company. We believe these programs will add to Lifecore’s high-value pipeline, and we expect each to contribute to the company’s long-term revenue growth objectives, beginning in 2027,” said Paul Josephs, president and chief executive officer of Lifecore. “In addition, early in the fourth quarter, we secured three new development-phase programs. These include one Phase 2 product with a top-20 global pharmaceutical company and two Phase 3 products with two biotech companies.”
Financial Snapshot
•Revenues for the third quarter of 2026 were $25.3 million, a decrease of $5.8 million, or 18.6% compared to $31.1 million for the prior year quarter ended September 30, 2025. Revenues for the nine months ended September 30, 2026, were $82.7 million, a decrease of $23.0 million, or 21.8% compared to $105.7 million for the nine months ended September 30, 2025.
•Gross profit for the quarter was $6.8 million, a decrease of $1.0 million compared to $7.8 million for the prior year quarter ended September 30, 2025. Gross profit for the nine months ended September 30, 2026, was $23.4 million, a decrease of $11.3 million compared to $34.7 million for the nine months ended September 30, 2025.
•Operating expenses for the third quarter were $7.7 million, a decrease of $3.1 million, or 28.9%, compared to $10.9 million for the prior year quarter ended September 30, 2025. Operating expenses for the nine months ended September 30, 2026, were $26.4 million, a decrease of $10.0 million, or 27.5%, compared to $36.4 million for the nine months ended September 30, 2025.
•Cash from operations was $9.5 million and free cash flow* was $6.9 million for the nine months ended September 30, 2026.
•Net loss for the third quarter of 2026 was $40.1 million or $1.08 loss per diluted share, as compared to net loss of $10.0 million or $0.29 loss per diluted share, for the prior year quarter ended September 30, 2025. Net loss for the nine months ended September 30, 2026, was $61.2 million or $1.70 loss per diluted share, as compared to net loss of $20.9 million or $0.64 loss per diluted share for the nine months ended September 30, 2025.
•Adjusted EBITDA* for the third quarter was $4.0 million, an increase of $1.0 million compared to $3.1 million for the prior year quarter ended September 30, 2025. Adjusted EBITDA* for the nine months ended September 30, 2026, was $13.6 million, a decrease of $7.4 million compared to $21.1 million for the nine months ended September 30, 2025.
•Ended the third quarter of 2026 with approximately $38.0 million in liquidity, including cash of $23.0 million and revolving credit availability of $15.0 million.



*    Adjusted EBITDA and free cash flow are non-GAAP financial measures and exclude certain items from net income or loss and operating cash flows, respectively, the nearest comparable measures calculated and presented in accordance with accounting principles generally accepted in the United States of America (“GAAP”). Please see “Non-GAAP Financial Information” below for more information, including definitions of Adjusted EBITDA and free cash flow and reconciliations to net loss and operating cash flows, respectively, for the periods noted in this press release.
Supplemental Financial Data
Supplemental Revenue and Gross Profit Data
Three months ended
September 30,
Change
20262025Amount%
(dollars in thousands)
Revenues:
CDMO
$17,777 $21,749 $(3,972)(18)%
HA manufacturing
7,545 9,360 (1,815)(19)%
Total revenues
25,322 31,109 (5,787)(19)%
Cost of sales
18,496 23,318 (4,822)(21)%
Gross profit6,826 7,791 (965)(12)%
Gross profit percentage27.0 %25.0 %2.0 %
Nine months ended
September 30,
Change
20262025Amount%
(dollars in thousands)
Revenues:
CDMO
$49,104 $69,382 $(20,278)(29)%
HA manufacturing
33,578 36,304 (2,726)(8)%
Total revenues
82,682 105,686 (23,004)(22)%
Cost of sales
59,319 70,981 (11,662)(16)%
Gross profit23,363 34,705 (11,342)(33)%
Gross profit percentage28.3 %32.8 %(4.5)%
Supplemental Operating Expense Data
Three months ended
September 30,
Change
20262025Amount%
(dollars in thousands)
Research and development$1,421 $1,963 $(542)(28)%
Selling, general and administrative6,299 8,895 (2,596)(29)%
Total operating expenses$7,720 $10,858 $(3,138)(29)%



Nine months ended
September 30,
Change
20262025Amount%
(dollars in thousands)
Research and development$4,175 $6,014 $(1,839)(31)%
Selling, general and administrative22,187 26,349 (4,162)(16)%
Restructuring recovery— (2,937)2,937 n/m
Loss on sale or disposal of assets, net of portion classified as cost of sales
— 6,942 (6,942)n/m
Total operating expenses$26,362 $36,368 $(10,006)(28)%
About Lifecore Biomedical
Lifecore Biomedical, Inc. (Nasdaq: LFCR) is a fully integrated contract development and manufacturing organization (CDMO) that offers highly differentiated capabilities in the development, fill and finish of sterile injectable pharmaceutical products in syringes, vials, and cartridges, including complex formulations. As a leading manufacturer of premium, injectable-grade hyaluronic acid, Lifecore brings more than 40 years of expertise as a partner for global and emerging biopharmaceutical and biotechnology companies across multiple therapeutic categories to bring their innovations to market. For more information about the company, visit Lifecore’s website at www.lifecore.com.
Non-GAAP Financial Information
In addition to providing financial measurements based on generally accepted accounting principles in the United States of America (GAAP), this press release contains non-GAAP financial information. Adjusted EBITDA and free cash flow are non-GAAP measures and exclude certain items from net income or loss and operating cash flows, respectively, which are the most directly comparable financial measures calculated in accordance with GAAP. See the section entitled “Non-GAAP Financial Reconciliations” below for the company’s definitions of Adjusted EBITDA and free cash flows and reconciliations to net income or loss and operating cash flows, respectively, for each period presented.
The company has disclosed these non-GAAP financial measures to supplement its consolidated financial statements presented in accordance with GAAP. These non-GAAP financial measures exclude/include certain items that are included in the company’s results reported in accordance with GAAP because we believe they are not reflective of our core operations or indicative of our ongoing operations. Management believes these non-GAAP financial measures provide useful additional information to investors about trends in the company’s operations and are useful for period-over-period comparisons. Management uses Adjusted EBITDA and free cash flow, in addition to GAAP financial measures, to monitor trends in the company’s operations, understand and compare operating results, and monitor cash flows across accounting periods, for financial and operational decision making, for planning and forecasting purposes, and with respect to Adjusted EBITDA as a measure of performance for compensation decisions.
These non-GAAP financial measures should not be considered in isolation or as a substitute for the comparable GAAP measures. In addition, these non-GAAP financial measures may not be the same as similar measures provided by other companies due to the potential differences in methods of calculation and items being excluded/included. These non-GAAP financial measures should be read in conjunction with the company’s consolidated financial statements presented in accordance with GAAP.



Important Cautions Regarding Forward-Looking Statements
This press release contains forward-looking statements regarding future events and our future results that are subject to the safe harbor created under the Private Securities Litigation Reform Act of 1995 and other safe harbors under the Securities Act of 1933 and the Securities Exchange Act of 1934. Words such as “anticipate”, “estimate”, “expect”, “project”, “aim,” “designed to,” “plan”, “intend”, “believe”, “may”, “might”, “will”, “should”, “can have”, “likely” and similar expressions are used to identify forward-looking statements. In addition, all statements regarding our future financial and operating performance and strategy, including our belief that the newly signed programs will be additive to our high-value pipeline, and our expectation that each will contribute to our long-term revenue growth objectives starting in 2027, are forward-looking statements. All forward-looking statements involve certain risks and uncertainties that could cause actual results to differ materially, including such factors as, among others, the timing and amount of future expenses, revenue, net income (loss), Adjusted EBITDA, cash flow and capital requirements, and timing and availability of and the need for additional financing; our ability to maintain or expand our relationships with our current customers, including the impact of changes in consumer demand for the products we manufacture for our customers; our ability to grow and diversify our business with new customers, including the potential loss of development customers if they do not receive required funding or regulatory approvals or for other reasons; our ability to comply with covenants under our credit agreements and to pay required interest and principal payments when due; our ability to fund or pay redemptions of shares of the outstanding Series A Convertible Preferred Stock in accordance with their terms; our ability to raise additional capital for ongoing needs, including through equity financing, debt financing, collaborations, strategic alliances or licensing arrangements; the impact of macroeconomic events or circumstances on our operations and financial performance, including inflation, tariffs, interest rates, social unrest and global instability; the performance of our third-party suppliers; pharmaceutical industry market forces that may impact our customers’ success and continued demand for the products we produce for those customers; our ability to recruit or retain key scientific, technical, business development, and management personnel and our executive officers; our ability to comply with stringent U.S. and foreign government regulation in the manufacture of pharmaceutical products, including current Good Manufacturing Practice, or cGMP; the outcome and cost of existing and any new litigation or regulatory proceedings; and other risk factors set forth from time to time in the company’s filings with the Securities and Exchange Commission (the “SEC”), including, but not limited to, the Transition Report on Form 10-KT for the transition period ended December 31, 2025 (the “December 2025 10-KT”). In addition, forward looking statements in this press release may be impacted by risks and uncertainties relating to the Company’s previously announced proposed merger pursuant to an Agreement and Plan of Merger dated September 27, 2026 among the Company, Lifecore Inc. and Hazel Merger Sub, Inc. These risks and uncertainties include, but are not limited to: (1) the proposed transaction may not be completed in a timely manner or at all, which may adversely affect Lifecore’s business and the price of its common stock; (2) the occurrence of any fact, event, change, development or circumstance that could give rise to the termination of the transaction agreement, including in circumstances requiring Lifecore to pay a termination fee; (3) the proposed transaction and its announcement could have an adverse effect on the ability of Lifecore to retain and hire key personnel and to maintain relationships with customers, vendors, partners, employees, stockholders and other business relationships and on its operating results and business generally; (4) risks related to the diversion of management’s attention from Lifecore’s ongoing business operations; (5) unexpected costs, charges or expenses resulting from the proposed transaction; (6) potential litigation relating to the proposed transaction that could be instituted against the parties to the transaction agreement or their respective directors, managers or officers, including the effects of any outcomes related thereto; (7) certain restrictions during the pendency of the proposed transaction that may impact Lifecore’s ability to make changes in its business, pursue certain business opportunities or strategic transactions; (8) uncertainties pertaining to other business effects, including the effects of industry, market, economic, political or regulatory conditions, future interest rates and changes in tax and other laws, regulations, rates and policies, and (9) the effect of the announcement or pendency of the transaction on Lifecore’s business, operating results and relationships with collaborators, vendors, competitors and others. For additional information about factors that could cause actual results to differ materially from those described in the forward-looking statements, please refer to our filings with the SEC, including the risk factors contained in the December 2025 10-KT and in our Quarterly Report on Form 10-Q for the quarter ended September 30, 2026.



Forward-looking statements represent management’s current expectations as of the date hereof and are inherently uncertain. Except as required by law, we do not undertake any obligation to update forward-looking statements made by us to reflect subsequent events or circumstances.
Lifecore Biomedical, Inc. Contact Information:
Stephanie Diaz (Investors)
Vida Strategic Partners
415-675-7401
sdiaz@vidasp.com
Jennifer Arcure (Media)
Vida Strategic Partners
917-603-0681
jarcure@vidasp.com
Ryan D. Lake (CFO)
Lifecore Biomedical
952-368-6244
ryan.lake@lifecore.com



LIFECORE BIOMEDICAL, INC.
CONSOLIDATED BALANCE SHEETS
(unaudited)
(in thousands, except share and per share amounts)September 30,
2026
December 31,
2025
ASSETS
Current assets:
Cash and cash equivalents$23,035 $17,469 
Accounts receivable, net9,077 13,233 
Accounts receivable, related party11,995 12,929 
Contract assets10,275 7,655 
Inventory
27,695 29,085 
Prepaid expenses and other current assets2,604 1,921 
Total current assets84,681 82,292 
Property, plant and equipment, net122,040 127,304 
Goodwill13,881 13,881 
Other assets7,701 8,700 
Total assets$228,303 $232,177 
LIABILITIES, CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current liabilities:
Accounts payable$8,587 $6,211 
Accrued expenses and other current liabilities13,453 17,362 
Total current liabilities22,040 23,573 
Debt, net of current portion
5,535 5,694 
Debt, net of current portion, related party
154,452 135,588 
Debt derivative liability, related party62,192 26,564 
Other liabilities
6,360 6,698 
Total liabilities250,579 198,117 
Commitments and contingencies
Series A Convertible Preferred Stock, $0.001 par value; 2,000,000 shares authorized; 50,187 and 47,466 shares issued and outstanding, redemption value $51,128 and $48,356
51,128 48,262 
Stockholders’ (deficit) equity:
Common Stock, $0.001 par value; 75,000,000 shares authorized; 37,905,846 and 37,477,386 shares issued and outstanding
38 37 
Additional paid-in capital210,979 208,962 
Accumulated deficit(284,421)(223,201)
Total stockholders’ deficit
(73,404)(14,202)
Total liabilities, convertible preferred stock and stockholders’ deficit
$228,303 $232,177 



LIFECORE BIOMEDICAL, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited)
Three months ended
September 30,
Nine months ended
September 30,
(in thousands, except share and per share amounts)
2026202520262025
Revenues$13,586 $19,293 $39,302 $57,314 
Revenues, related party11,736 11,816 43,380 48,372 
Total revenues25,322 31,109 82,682 105,686 
Cost of sales18,496 23,318 59,319 70,981 
Gross profit6,826 7,791 23,363 34,705 
Research and development expenses1,421 1,963 4,175 6,014 
Selling, general, and administrative expenses6,299 8,895 22,187 26,349 
Restructuring recovery— — — (2,937)
Loss on sale or disposal of assets, net of portion classified as cost of sales— — — 6,942 
Operating loss
(894)(3,067)(2,999)(1,663)
Interest income
232 58 504 472 
Interest expense
(425)(551)(1,359)(1,721)
Interest expense, related party(7,675)(5,833)(21,840)(16,031)
Change in fair value of debt derivative liability, related party(31,270)(375)(35,628)(1,991)
Other (expense) income, net
(1)110 219 359 
Loss before income taxes
(40,033)(9,658)(61,103)(20,575)
Income tax expense
(51)(333)(117)(359)
Net loss
(40,084)(9,991)(61,220)(20,934)
Preferred stock dividends
(941)(874)(2,772)(2,573)
Accretion of preferred stock to redemption value
— (48)(94)(144)
Loss available to common stockholders
$(41,025)$(10,913)$(64,086)$(23,651)
Loss per share, basic and diluted
$(1.08)$(0.29)$(1.70)$(0.64)
Weighted average shares outstanding, basic and diluted37,845,478 37,402,912 37,633,816 37,148,750 



Non-GAAP Financial Reconciliations
Adjusted EBITDA is a non-GAAP financial measure and excludes certain items from net income or loss, the most directly comparable financial measure calculated in accordance with GAAP. For the periods presented herein, we defined Adjusted EBITDA as net income or loss before (i) interest expense, net of interest income, (ii) income tax expense or benefit, (iii) depreciation, (iv) stock-based compensation, (v) change in fair value of debt derivatives, (vi) franchise tax, (vii) reorganization costs, (viii) restructuring costs or recovery, and (ix) loss on sale or disposal of assets. See “Non-GAAP Financial Information” above for further information regarding the company’s use of non-GAAP financial measures.
Three months ended
September 30,
Nine months ended
September 30,
(in thousands) (unaudited)
2026202520262025
Net loss (GAAP)
$(40,084)$(9,991)$(61,220)$(20,934)
Interest expense, net7,868 6,326 22,695 17,280 
Income tax expense51 333 117 359 
Depreciation2,410 1,981 7,235 5,968 
Stock-based compensation1,715 2,392 5,498 6,404 
Change in fair value of debt derivatives31,270 375 35,628 1,991 
Franchise tax52 63 152 83 
Reorganization costs
720 1,571 3,509 5,104 
Restructuring recovery
— — — (2,937)
Loss on sale or disposal of assets— — — 7,738 
Adjusted EBITDA$4,002 $3,050 $13,614 $21,056 
Free cash flow is a non-GAAP financial measure that reduces operating cash flows, the most directly comparable financial measure calculated in accordance with GAAP, by capital expenditures. See “Non-GAAP Financial Information” above for further information regarding the company’s use of non-GAAP financial measures.
Nine months ended
September 30,
(in thousands) (unaudited)
20262025
Operating cash flows (GAAP)$9,457 $12,506 
Less: capital expenditures(2,543)(9,792)
Free cash flow$6,914 $2,714 

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