Cerus (Nasdaq: CERS) grows 2025 revenue 16% and reaffirms 2026 outlook
Rhea-AI Filing Summary
Cerus Corporation reported strong 2025 growth with total revenue of $233.8 million, up 16% from 2024. Product revenue rose 14% to $206.1 million, helped by expansion of its INTERCEPT platelet franchise and higher U.S. INTERCEPT Fibrinogen Complex (IFC) sales.
IFC revenue increased about 80% to $16.7 million, and total product gross profit reached $112.3 million with a 54.5% margin, slightly below last year. Net loss narrowed to $15.6 million (or $0.08 per share), while non-GAAP adjusted EBITDA improved to $9.5 million. Cerus ended 2025 with $82.9 million in cash, cash equivalents and short-term investments and generated $4.8 million in operating cash flow for the year. For 2026, the company reaffirms product revenue guidance of $224–$228 million, implying 9%–11% growth, including expected IFC revenue of $20–$22 million, or roughly 20%–30% growth.
Positive
- Strong top-line growth and improving EBITDA: 2025 total revenue rose 16% to $233.8 million, product revenue grew 14% to $206.1 million, and non-GAAP adjusted EBITDA increased to $9.5 million from $5.7 million, showing better operating leverage.
Negative
- Business still loss-making with modest margin compression: Net loss attributable to Cerus remained sizable at $15.6 million in 2025 and product gross margin declined from 55.2% to 54.5%, reflecting higher production costs and macro pressures.
Insights
Double‑digit revenue growth and improving cash metrics, but business remains loss‑making.
Cerus delivered a solid 2025 with total revenue of
Profitability metrics are improving but not fully resolved. Product gross margin dipped slightly to
Liquidity appears stable, with
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): |
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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:
Securities registered pursuant to Section 12(b) of the Act:
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Trading |
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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 March 2, 2026, Cerus Corporation (the “Company”) announced its financial results for its fourth quarter and fiscal year ended December 31, 2025. A copy of the Company’s press release, entitled “Cerus Corporation Announces Full-Year and Fourth Quarter 2025 Financial Results,” is furnished pursuant to Item 2.02 as Exhibit 99.1 hereto.
The information in this report, including the exhibit hereto, shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of Section 11 and 12(a)(2) of the Securities Act of 1933, as amended. The information contained herein and in the accompanying exhibit shall not be incorporated by reference into any filing with the U.S. Securities and Exchange Commission made by the Company, whether made before or after the date hereof, except as shall be expressly set forth by specific reference in such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
The following exhibit is furnished with this report:
99.1 Press release, dated March 2, 2026, entitled “Cerus Corporation Announces Full-Year and Fourth Quarter 2025 Financial Results.”
104 Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101)
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 hereunto duly authorized.
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CERUS CORPORATION |
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Date: |
March 2, 2026 |
By: |
/s/ Kevin D. Green |
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Kevin D. Green, Chief Financial Officer |
Exhibit 99.1
Cerus Corporation Announces Full-Year and Fourth Quarter 2025 Financial Results
2025 Total Revenue of $233.8 million, up 16% from 2024; 2025 Product Revenue of $206.1 million, up 14% from 2024
Strengthened Financial Foundation Through Strong Commercial Execution and Disciplined Operational Management
CONCORD, CA, March 2, 2026 - Cerus Corporation (Nasdaq: CERS) announced today financial results for its full year and fourth quarter ended December 31, 2025.
“Our strong 2025 results reflect our disciplined execution, as we continued to deliver on our mission of safeguarding the world’s blood supply. This past year, we achieved our highest annual kit shipments, enabling an estimated 600,000 patients worldwide to receive INTERCEPT-treated blood components,” said William “Obi” Greenman, Cerus’ president and chief executive officer. “This translated into record product revenue of over $206 million, a narrowing of our GAAP net loss, and positive non-GAAP adjusted EBITDA for the second consecutive year. Looking ahead to 2026, we remain focused on improving global access to our INTERCEPT technologies, advancing our product development programs and building upon the solid financial foundation we have established.”
Additional highlights include:
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Three Months Ended |
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Twelve Months Ended |
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December 31, |
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Change |
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December 31, |
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Change |
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2025 |
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2024 |
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$ |
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% |
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2025 |
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2024 |
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$ |
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% |
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Product Revenue |
$ |
57.8 |
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$ |
50.8 |
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$ |
7.0 |
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14 |
% |
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$ |
206.1 |
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$ |
180.3 |
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$ |
25.8 |
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14 |
% |
Government Contract Revenue |
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6.8 |
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5.9 |
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0.9 |
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15 |
% |
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27.7 |
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21.1 |
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6.6 |
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31 |
% |
Total Revenue |
$ |
64.6 |
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$ |
56.8 |
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$ |
7.8 |
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14 |
% |
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$ |
233.8 |
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$ |
201.3 |
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$ |
32.5 |
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16 |
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Numbers may not sum due to rounding. Percentages calculated from unrounded figures. |
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Revenue
Product revenue for the fourth quarter of 2025 was $57.8 million, compared to $50.8 million for the prior year period, representing year-over-year growth of 14%. Fourth quarter growth was primarily driven by strength in EMEA across the platelets franchise and continued rollout of INT200, as well as increased U.S. IFC sales. Product revenue for the full year 2025 was $206.1 million, compared to $180.3 million for the prior year, representing 14% growth. Full-year growth was driven by continued expansion of the Company’s global platelet products, increased U.S. IFC sales, and the launch of INT200 in EMEA.
Government contract revenue for the fourth quarter of 2025 was $6.8 million, compared to $5.9 million during the prior year period. Full year 2025 government contract revenue was $27.7 million, compared to $21.1 million during the prior year period. The increase in fourth quarter and full year government contract revenue was largely driven by BARDA-related projects.
Product Gross Profit and Margin
Product gross profit for the fourth quarter of 2025 was $29.7 million, increasing by 9% over the prior year period. Product gross margin for the fourth quarter of 2025 was 51.5% compared to 53.9% in the same period last year. Full-year 2025 product gross profit was $112.3 million, representing 13% growth compared to 2024. Full-year product gross margin was 54.5%, compared to 55.2% in the prior year. Higher IFC therapeutic production costs, ongoing trade regulation and inflationary pressures, as well as foreign exchange rates contributed to the change in product gross margin percentage compared to the prior year for both periods.
Operating Expenses
Total operating expenses for the fourth quarter of 2025 were $37.2 million, compared to $34.8 million in the same period of the prior year, representing a 7% year-over-year increase. For the full year 2025, total operating expenses were $148.6 million, compared to $134.8 million in 2024.
Research and development (R&D) expenses for the fourth quarter of 2025 were $16.4 million, compared to $15.4 million in the prior year period. For the full year 2025, R&D expenses totaled $67.7 million, compared to $58.9 million in 2024. Higher government contract costs and workforce-related costs contributed to the increase in R&D expenses for the fourth quarter. For the full year, the increase was driven by the same factors as well as increased development costs associated with the Company’s red blood cell and INT200 programs.
Selling, general, and administrative (SG&A) expenses for the fourth quarter of 2025 were $20.8 million, compared to $19.3 million in the prior year period. For the full year 2025, SG&A expenses totaled $80.9 million, compared to $75.9 million for the full year 2024.
Net Loss Attributable to Cerus Corporation
Net loss attributable to Cerus Corporation narrowed for the fourth quarter of 2025 and was $2.2 million, or $0.01 per basic and diluted share, compared to $2.5 million, or $0.01 per basic and diluted share, for the fourth quarter of 2024.
For the full year 2025, net loss attributable to Cerus Corporation was $15.6 million, or $0.08 per basic and diluted share, compared to $20.9 million, or $0.11 per basic and diluted share, in 2024.
Non-GAAP Adjusted EBITDA
2
Non-GAAP adjusted EBITDA for the fourth quarter of 2025 was $3.4 million, compared to $3.3 million for the fourth quarter of 2024. Full-year 2025 non-GAAP adjusted EBITDA was $9.5 million, compared to $5.7 million in 2024. For additional information, please see definitions and the reconciliation of this non-GAAP measure to net loss attributable to Cerus Corporation accompanying this release.
Balance Sheet and Cash Flows
At December 31, 2025, the Company had $82.9 million in cash, cash equivalents and short-term investments, compared to $80.5 million at December 31, 2024.
As of December 31, 2025, the Company had $65.0 million outstanding on its term loan and $19.0 million drawn on its revolving credit facility. The Company’s revolving line of credit allows for an additional $16.0 million as of December 31, 2025, which is dependent on eligible assets supporting the borrowing base.
For the fourth quarter of 2025, the Company generated $6.2 million in operating cash flow, compared to $4.9 million in the prior year period. The Company generated $8.1 million of operating cash flow in the second half of 2025 offsetting operating cash used during the first half of 2025. As a result, for the full year 2025, the Company generated $4.8 million in operating cash flow, compared to $11.4 million generated during 2024. These results were consistent with the Company’s previously communicated expectations which anticipated first-half cash use related to inventory investment, followed by stronger operating cash flow in the second half of 2025.
Reaffirming 2026 Product Revenue Guidance
The Company expects full-year 2026 product revenue to be in the range of $224 million to $228 million, representing year-over-year growth of 9% to 11% compared to 2025 product revenue. Included in the 2026 guidance range is expected full-year 2026 IFC revenue of $20 million to $22 million, representing year-over-year growth of approximately 20% to 30% from 2025.
Quarterly Conference Call
The Company will host a conference call at 4:30 P.M. ET this afternoon, during which management will discuss the Company’s financial results and provide a general business overview and outlook. To listen to the live webcast, please visit the Investor Relations page of the Cerus website at http://www.cerus.com/ir.
A replay will be available on Cerus’ website approximately three hours after the call through March 23, 2026.
*FC15 equivalent to a therapeutic dose of a cryoAHF pool.
ABOUT CERUS
Cerus Corporation is dedicated solely to safeguarding the world’s blood supply and aims to become the preeminent global blood products company. Headquartered in Concord, California, the company develops and supplies vital technologies and pathogen-protected blood components to blood centers, hospitals, and ultimately patients who rely on safe blood. The INTERCEPT Blood System for platelets and plasma is available globally and remains the only pathogen reduction system with both CE mark and FDA approval for these two blood components. In the U.S., the INTERCEPT Blood System for Cryoprecipitation is approved for the production of Pathogen Reduced Cryoprecipitated Fibrinogen Complex (commonly referred to as INTERCEPT Fibrinogen Complex), a therapeutic product for the treatment and control of bleeding, including massive hemorrhage, associated with fibrinogen deficiency. The INTERCEPT red blood cell system is under
3
regulatory review in Europe, and in late-stage clinical development in the U.S. For more information about Cerus, visit www.cerus.com and follow us on LinkedIn.
Cerus, INTERCEPT and the Cerus logo are trademarks of Cerus Corporation.
Forward-Looking Statements
Except for the historical statements contained herein, this press release contains forward-looking statements concerning Cerus’ products, prospects and expected results, including statements relating to: Cerus’ expectation that full-year 2026 product revenue will be in the range of $224 million to $228 million, including IFC revenue of between $20 million and $22 million; Cerus’ expectation that full-year 2026 product revenue will grow 9% to 11% year over year; Cerus continuing to have access to $16.0 million under its revolving line of credit; Cerus’ ability to continue to improve global access to its INTERCEPT technologies; Cerus’ ability to advance our product development programs; the continued commercialization and launch of INT200 and IFC; and other statements that are not historical fact. Actual results could differ materially from these forward-looking statements as a result of certain factors, including, without limitation: risks associated with the commercialization and market acceptance of, and customer demand for, the INTERCEPT Blood System and IFC; the risk that Cerus may not meet its 2026 annual product revenue guidance; the risk that Cerus may not effectively continue to launch and commercialize the INTERCEPT Blood System for Cryoprecipitation or INT200; the risk that Cerus may not grow sales globally, including in its U.S. and European markets, and/or realize expected revenue contributions resulting from its U.S. and European market agreements; risks related to the uncertain and time-consuming development and regulatory process, including the risk that Cerus may be unable to obtain requisite regulatory approvals to advance its pipeline programs and bring them to market in a timely manner or at all; risks associated with macroeconomic developments, including ongoing military conflict in Ukraine, new or increased tariffs and escalating trade tensions, inflation, rising interest rates and foreign exchange volatility and the resulting global economic and financial disruptions; risks related to Cerus’ ability to demonstrate to the transfusion medicine community and other healthcare constituencies that pathogen reduction and the INTERCEPT Blood System are safe, effective and economical; risks related to product safety; risks associated with Cerus’ ability to maintain an effective, secure manufacturing supply chain, including risks that (a) Cerus’ supply chain could be negatively impacted as a result of macroeconomic developments, (b) Cerus’ manufacturers could be unable to comply with extensive regulatory agency requirements, and (c) Cerus may be unable to maintain its supply agreements with its third-party suppliers; risks associated with Cerus’ ability to access additional funds under its credit facility and to meet its debt service obligations, and its need for additional funding; risks associated with the impact of legislative or regulatory healthcare reforms that may make it more difficult and costly for Cerus to produce, market and distribute its products; as well as other risks detailed in Cerus’ filings with the Securities and Exchange Commission, including under the heading “Risk Factors” in Cerus’ Annual Report on Form 10-K for the year ended December 31, 2024, filed with the SEC on February 26, 2025 and Quarterly Report on Form 10-Q for the quarter ended September 30, 2025. Cerus disclaims any obligation or undertaking to update or revise any forward-looking statements contained in this press release.
Use of Non-GAAP Financial Measures
We define adjusted EBITDA as net loss attributable to Cerus Corporation as reported on the consolidated statement of operations, as adjusted to exclude, as applicable for the reporting period(s) presented, (i) net loss attributable to noncontrolling interest, (ii) provision for income taxes, (iii) foreign exchange (loss)/gain, (iv) interest income (expense), (v) other income (expense), net, (vi) depreciation and amortization, (vii) share-based compensation, (viii) goodwill and asset impairments, (ix) costs associated with our noncontrolling interest in our joint venture in China and, (x) revenue and direct costs associated with our government contracts. We are presenting this non-GAAP financial measure to assist investors in assessing our operating results. Management believes this non-GAAP information is useful for investors, when considered in
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conjunction with Cerus’ GAAP financial statements, because management uses such information internally for its operating, budgeting and financial planning purposes. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of Cerus’ operating results as reported under GAAP. This non-GAAP financial measure should not be considered in isolation from, or as a substitute for, financial information prepared in accordance with GAAP. This non-GAAP financial measure is not necessarily comparable to similarly-titled measures presented by other companies.
Contact:
Tim Lee – Head of Investor Relations
Cerus Corporation
ir@cerus.com
925-288-6128
5
Supplemental Tables
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Three Months Ended |
Twelve Months Ended |
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December 31, |
December 31, |
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2025 vs. 2024 |
2025 vs. 2024 |
Platelet Kit Growth |
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North America |
-3% |
4% |
International |
6% |
4% |
Worldwide |
0% |
4% |
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Change in Calculated Number of Treatable Platelet Doses |
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North America |
-3% |
4% |
International |
4% |
2% |
Worldwide |
-1% |
3% |
Dose treatable calculation based on the number of kits sold and the product configuration (single, double, and triple dose kits) |
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CERUS CORPORATION |
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REVENUE BY REGION |
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(in thousands, except percentages) |
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Three Months Ended |
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Twelve Months Ended |
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December 31, |
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Change |
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December 31, |
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Change |
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2025 |
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2024 |
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$ |
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% |
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2025 |
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2024 |
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$ |
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% |
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North America |
$ |
34,960 |
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$ |
33,270 |
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$ |
1,690 |
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5 |
% |
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$ |
135,875 |
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$ |
119,978 |
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$ |
15,897 |
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13 |
% |
Europe, Middle East and Africa |
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21,801 |
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16,080 |
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5,721 |
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36 |
% |
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67,370 |
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56,327 |
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11,043 |
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20 |
% |
Other |
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990 |
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1,459 |
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(469 |
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-32 |
% |
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2,888 |
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3,965 |
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(1,077 |
) |
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-27 |
% |
Total product revenue |
$ |
57,751 |
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$ |
50,809 |
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$ |
6,942 |
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14 |
% |
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$ |
206,133 |
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$ |
180,270 |
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$ |
25,863 |
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14 |
% |
7
CERUS CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share data)
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Unaudited Three Months Ended |
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Twelve Months Ended |
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December 31, |
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December 31, |
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Unaudited |
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Audited |
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2025 |
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2024 |
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2025 |
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2024 |
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Product revenue |
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$ |
57,751 |
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$ |
50,809 |
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$ |
206,133 |
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$ |
180,270 |
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Cost of product revenue |
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28,002 |
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23,424 |
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93,845 |
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80,748 |
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Gross profit on product revenue |
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29,749 |
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27,385 |
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112,288 |
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99,522 |
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Government contract revenue |
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6,828 |
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5,942 |
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27,665 |
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21,051 |
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Operating expenses: |
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Research and development |
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16,390 |
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15,443 |
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67,720 |
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58,907 |
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Selling, general and administrative |
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20,828 |
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19,333 |
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80,914 |
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75,891 |
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Total operating expenses |
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37,218 |
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34,776 |
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148,634 |
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134,798 |
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Loss from operations |
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(641 |
) |
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(1,449 |
) |
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(8,681 |
) |
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(14,225 |
) |
Total non-operating expense, net |
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(1,424 |
) |
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(1,002 |
) |
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(6,602 |
) |
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(6,531 |
) |
Loss before income taxes |
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(2,065 |
) |
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|
(2,451 |
) |
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(15,283 |
) |
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(20,756 |
) |
Provision for income taxes |
|
|
119 |
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|
111 |
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|
354 |
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|
205 |
|
Net loss |
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|
(2,184 |
) |
|
|
(2,562 |
) |
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|
(15,637 |
) |
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|
(20,961 |
) |
Net loss attributable to noncontrolling interest |
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- |
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(41 |
) |
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(10 |
) |
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(43 |
) |
Net loss attributable to Cerus Corporation |
|
$ |
(2,184 |
) |
|
$ |
(2,521 |
) |
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$ |
(15,627 |
) |
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$ |
(20,918 |
) |
Net loss per share attributable to Cerus Corporation: |
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Basic and diluted |
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$ |
(0.01 |
) |
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$ |
(0.01 |
) |
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$ |
(0.08 |
) |
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$ |
(0.11 |
) |
Weighted average shares outstanding: |
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Basic and diluted |
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192,109 |
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185,734 |
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190,594 |
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|
184,563 |
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8
CERUS CORPORATION
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands)
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December 31, |
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December 31, |
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2025 |
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2024 |
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(unaudited) |
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(audited) |
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ASSETS |
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Current assets: |
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Cash and cash equivalents |
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$ |
19,961 |
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$ |
20,266 |
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Short-term investments |
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|
62,918 |
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|
60,186 |
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Accounts receivable, net |
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|
30,374 |
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|
29,777 |
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Current inventories |
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|
56,101 |
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|
38,150 |
|
Prepaid and other current assets |
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|
5,030 |
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|
3,643 |
|
Total current assets |
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174,384 |
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|
152,022 |
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Non-current assets: |
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Property and equipment, net |
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|
9,204 |
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|
7,154 |
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Operating lease right-of-use assets |
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|
10,124 |
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|
8,384 |
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Goodwill |
|
|
1,316 |
|
|
|
1,316 |
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Non-current inventories |
|
|
15,143 |
|
|
|
14,145 |
|
Other assets and restricted cash |
|
|
11,688 |
|
|
|
17,896 |
|
Total assets |
|
$ |
221,859 |
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|
$ |
200,917 |
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|
||
LIABILITIES AND STOCKHOLDERS' EQUITY |
|
|
|
|
|
|
||
Current liabilities: |
|
|
|
|
|
|
||
Accounts payable and accrued liabilities |
|
$ |
53,279 |
|
|
$ |
40,638 |
|
Debt – current |
|
|
43,343 |
|
|
|
19,297 |
|
Operating lease liabilities – current |
|
|
2,905 |
|
|
|
2,275 |
|
Deferred revenue – current |
|
|
1,274 |
|
|
|
1,398 |
|
Total current liabilities |
|
|
100,801 |
|
|
|
63,608 |
|
Non-current liabilities: |
|
|
|
|
|
|
||
Debt – non-current |
|
|
40,545 |
|
|
|
64,862 |
|
Operating lease liabilities – non-current |
|
|
10,153 |
|
|
|
11,663 |
|
Other non-current liabilities |
|
|
5,395 |
|
|
|
3,888 |
|
Total liabilities |
|
|
156,894 |
|
|
|
144,021 |
|
Stockholders' equity: |
|
|
64,224 |
|
|
|
56,145 |
|
Noncontrolling interest |
|
|
741 |
|
|
|
751 |
|
Total liabilities and stockholders' equity |
|
$ |
221,859 |
|
|
$ |
200,917 |
|
|
|
|
|
|
|
|
||
9
CERUS CORPORATION |
|
|
||||||||||||||
UNAUDITED RECONCILIATION OF NON-GAAP ADJUSTED EBITDA |
|
|
||||||||||||||
(in thousands) |
|
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
|
Three Months Ended |
|
|
Twelve Months Ended |
|
|
||||||||||
|
December 31, |
|
|
December 31, |
|
|
||||||||||
|
2025 |
|
|
2024 |
|
|
2025 |
|
|
2024 |
|
|
||||
Net loss attributable to Cerus Corporation |
$ |
(2,184 |
) |
|
$ |
(2,521 |
) |
|
$ |
(15,627 |
) |
|
$ |
(20,918 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
Adjustments to net loss attributable to Cerus Corporation: |
|
|
|
|
|
|
|
|
|
|
|
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
Net loss attributable to noncontrolling interest |
|
- |
|
|
|
(41 |
) |
|
|
(10 |
) |
|
|
(43 |
) |
|
Provision for income taxes |
|
119 |
|
|
|
111 |
|
|
|
354 |
|
|
|
205 |
|
|
Total non-operating expense, net (i) |
|
1,424 |
|
|
|
1,002 |
|
|
|
6,602 |
|
|
|
6,531 |
|
|
Loss from operations |
|
(641 |
) |
|
|
(1,449 |
) |
|
|
(8,681 |
) |
|
|
(14,225 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
Adjustments to loss from operations: |
|
|
|
|
|
|
|
|
|
|
|
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
Operating depreciation and amortization |
|
1,108 |
|
|
|
1,104 |
|
|
|
4,240 |
|
|
|
4,568 |
|
|
Government contract revenue (ii) |
|
(6,828 |
) |
|
|
(5,942 |
) |
|
|
(27,665 |
) |
|
|
(21,051 |
) |
|
Direct expenses attributable to government contracts (iii) |
|
4,797 |
|
|
|
3,975 |
|
|
|
18,705 |
|
|
|
13,488 |
|
|
Share-based compensation (iv) |
|
4,927 |
|
|
|
5,504 |
|
|
|
22,867 |
|
|
|
22,867 |
|
|
Costs attributable to noncontrolling interest (v) |
|
- |
|
|
|
82 |
|
|
|
21 |
|
|
|
85 |
|
|
Non-GAAP adjusted EBITDA |
$ |
3,363 |
|
|
$ |
3,274 |
|
|
$ |
9,487 |
|
|
$ |
5,732 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
i. Includes interest income/expense and foreign exchange gains/losses. |
||||||||||||||||
ii. Represents revenue related to the cost reimbursement provisions under our government contracts. |
||||||||||||||||
iii. Represents the direct expenses attributable to work supporting government contracts, which are reimbursed and reflect under government contract revenue in the condensed consolidated statement of operations. |
||||||||||||||||
iv. Represents non-cash stock-based compensation. |
||||||||||||||||
v. Represents costs associated with the noncontrolling interest in Cerus Zhongbaokang (Shandong) Biomedical Co., LTD. |
||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
10
FAQ
How did Cerus (CERS) perform financially in 2025?
What drove Cerus Corporation’s 2025 revenue growth?
What guidance did Cerus (CERS) give for 2026 product revenue?
Is Cerus Corporation profitable on a GAAP basis?
What is Cerus Corporation’s cash and debt position at year-end 2025?
How did Cerus’ INTERCEPT Fibrinogen Complex (IFC) business perform in 2025?
Filing Exhibits & Attachments
2 documentsPress Releases
