STOCK TITAN

Cryoport raises 2026 revenue guidance to $197M-$199M

Commercial cell and gene therapy clients generated 20% year-over-year revenue growth in the third quarter.

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Form Type
8-K

Rhea-AI Filing Summary

Cryoport, Inc. reported third-quarter 2026 revenue of $50.220 million, up 14% from $44.233 million a year earlier. Life Sciences Services revenue increased 18% to $28.564 million, including 25% growth in BioStorage/BioServices; Life Sciences Products revenue rose 8% to $21.656 million. For the first nine months, revenue was $146.989 million, compared with $130.727 million. Life Sciences Services revenue was $83.431 million and Life Sciences Products revenue was $63.558 million during that period.

GAAP loss from continuing operations was $10.852 million, versus $6.696 million a year earlier, while adjusted EBITDA from continuing operations was $1.103 million, compared with a $649,000 loss. For the first nine months, adjusted EBITDA from continuing operations was $867,000, compared with a $4.382 million loss a year earlier. Cryoport raised full-year 2026 revenue guidance to $197 million to $199 million. As of September 30, 2026, Cryoport supported 23 commercial therapies and 788 clinical trials, including 99 Phase 3 trials. Cash and cash equivalents were $279.179 million and short-term investments were $113.897 million as of that date.

2 points · 0 major

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0 major · 1 point

How the balance works

Positive

  • Moderate pointQ3 revenue was $50.220 million, up 14% year over year.
  • Moderate pointQ3 adjusted EBITDA from continuing operations was $1.103 million.

Negative

  • Moderate pointQ3 continuing-operations loss was $10.852 million, versus $6.696 million.

Filing Explained

Cryoport’s November 5 8-K reports third-quarter results; as of September 30, 2026, its balance sheet listed current convertible notes alongside cash and short-term investments.

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.
Q3 total revenue $50.220 million Q3 2026; up 14% from Q3 2025
Life Sciences Services revenue $28.564 million Q3 2026; up 18% year over year
Life Sciences Products revenue $21.656 million Q3 2026; up 8% year over year
Loss from continuing operations ($10.852 million) Q3 2026; compared with ($6.696 million) in Q3 2025
Adjusted EBITDA from continuing operations $1.103 million Q3 2026; compared with a $649,000 loss in Q3 2025
Full-year revenue guidance $197 million to $199 million Full-year 2026; raised guidance
Supported clinical trials 788 trials As of September 30, 2026; includes 99 Phase 3 trials
Adjusted EBITDA from continuing operations financial
"positive adjusted EBITDA of $1.1 million for the quarter"
Earnings before interest, taxes, depreciation and amortization (EBITDA) from continuing operations is a measure of a company’s recurring operating profit that excludes discontinued business lines. Companies further adjust that EBITDA by removing one-time, noncash, or irregular items (for example restructuring costs or gains on asset sales) to show the underlying trend. For investors it is meant to act like a cleaned-up household budget that highlights core, ongoing business performance, though what gets adjusted can vary between companies.
discontinued operations financial
"presented as discontinued operations for all periods"
Discontinued operations are parts of a company that it has decided to sell or shut down, and no longer plans to run in the future. This matters to investors because it helps them understand which parts of the business are ongoing and which are being phased out, providing a clearer picture of the company’s current performance and future prospects. Think of it like a store closing a department—it no longer contributes to sales or profits.
Biologics License Applications (BLA) regulatory
"filed Biologics License Applications (BLA) with the FDA"
A Biologics License Application (BLA) is the formal submission to the U.S. Food and Drug Administration seeking permission to market a biological product, such as a vaccine, therapeutic antibody, or cell therapy. The filing packages clinical trial results, safety data and details about how the product is made; approval is like getting a commercial operating license that lets the company sell the product. Investors watch BLAs closely because approval or rejection directly affects a company’s ability to generate revenue and the stock’s valuation, while the timing and regulatory risks influence investment decisions.
Marketing Authorization Applications (MAA) regulatory
"possible BLA or Marketing Authorization Applications (MAA)"
A marketing authorization application (MAA) is a formal package submitted to a health regulator asking for permission to sell a medicine or medical product; it includes evidence about safety, effectiveness and how the product is made. Investors care because approval is the gate that allows a product to reach the market and generate revenue, so the status and timing of an MAA are key drivers of a company’s future sales prospects and valuation — like applying for a business license before opening a store.
Prescription Drug User Fee Act (PDUFA) dates regulatory
"received Prescription Drug User Fee Act (PDUFA) dates from the FDA"
accelerated approval regulatory
"received accelerated U.S. Food and Drug Administration (FDA) approval"
Accelerated approval is a process that allows new medical treatments to be approved more quickly than usual if they address serious or life-threatening conditions and show promising early results. For investors, it signals that a treatment may reach the market sooner, potentially boosting a company's prospects, but it also involves some uncertainty since full evidence of effectiveness is still being gathered.
Revenue $50.220 million 14% year-over-year increase from $44.233 million
Loss from continuing operations ($10.852 million) Compared with ($6.696 million) in Q3 2025
Adjusted EBITDA from continuing operations $1.103 million Compared with a $649,000 loss in Q3 2025
Guidance

Full-year 2026 revenue guidance was raised to $197 million to $199 million.

FAQ

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

What revenue did CYRX report in Q3 2026?

Cryoport reported Q3 2026 revenue of $50.220 million, up 14% from $44.233 million in Q3 2025. Life Sciences Services revenue was $28.564 million, and Life Sciences Products revenue was $21.656 million.

What is CYRX's full-year 2026 revenue guidance?

Cryoport raised its full-year 2026 revenue guidance to $197 million to $199 million. The company cited its year-to-date performance, expanding support of commercial therapies, customer relationships, clinical-trial pipeline and demand for MVE products.

How many Phase 1, Phase 2 and Phase 3 clinical trials did CYRX support?

As of September 30, 2026, Cryoport supported 319 Phase 1, 370 Phase 2 and 99 Phase 3 clinical trials. The company reported 788 supported trials overall, a net increase of 43 from September 30, 2025.

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

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, DC 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 5, 2026

 

CRYOPORT, INC. 

(Exact name of registrant as specified in its charter)

 

Nevada   001-34632   88-0313393
(State or other jurisdiction
of incorporation)
  (Commission File Number)   (IRS Employer
Identification No.)
         

112 Westwood Place, Suite 350, Brentwood, TN 37027

(Address of principal executive offices, including zip code)
         
Registrant’s telephone number, including area code: (949) 470-2300
 
Not Applicable
(Former name or former address, if changed since last report)

  

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

 

¨ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
     
¨ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
     
¨ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
     
¨ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
     

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

 

Title of each class   Trading Symbol   Name of each exchange on which
registered
Common Stock, $0.001 par value   CYRX   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 2.02Results of Operations and Financial Condition.

 

On November 5, 2026, Cryoport, Inc. (the “Company”) issued a press release announcing its financial results for the third quarter ended September 30, 2026. A copy of the press release issued by the Company is attached hereto as Exhibit 99.1.

 

The information, including the exhibit attached hereto, in this Current Report on Form 8-K 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 in any filing under the Securities Act of 1933 or the Exchange Act, except as otherwise expressly stated in such filing.

 

Item 9.01. Financial Statements and Exhibits

 

(d) Exhibits. The following material is filed as an exhibit to this Current Report on Form 8-K:

  

Exhibit

Number

  
   
99.1 Press Release dated November 5, 2026 issued by the Company.
   
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 hereunto duly authorized.

 

Date: November 5, 2026 Cryoport, Inc.
   
  /s/ Robert Stefanovich
  Robert Stefanovich
  Chief Financial Officer

 

 

 

 

 

Exhibit 99.1

 

 

Cryoport Reports Third Quarter 2026 Financial Results

 

·Third quarter revenue grew 14% year-over-year to $50.2 million

 

·Commercial Cell and Gene Therapy revenue increased 20% year-over-year

 

·Supporting a record 788 global clinical trials and 23 commercially approved cell and gene therapies as of September 30, 2026

 

·Raises full-year 2026 revenue guidance to $197 million - $199 million

 

NASHVILLE, Tennessee, November 5, 2026, - Cryoport, Inc. (NASDAQ: CYRX) (“Cryoport” or the “Company”), a leading global provider of integrated temperature-controlled supply chain solutions for the life sciences, today announced financial results for its third quarter (Q3) and first nine months (9M) of 2026.

 

Jerrell Shelton, CEO of Cryoport, stated, “Cryoport delivered third quarter revenue of $50.2 million, reflecting continued momentum across our core cell and gene therapy (CGT) business. Revenue from commercial CGT clients increased 20% year over year, BioStorage/BioServices revenue expanded 25%, and total Life Sciences Services revenue grew 18%, underscoring the strength of our integrated platform and the growing demand for our solutions. These results reflect both the increasing number of patients worldwide receiving CGT treatments and the continued adoption of our end-to-end temperature-controlled supply chain solutions. We also achieved 8% year over year growth in Life Sciences Products revenue, supported by MVE Biological Solutions’ (MVE) position as the global market leader in cryogenic systems.”

 

“During the quarter, we further strengthened our leadership position within the CGT ecosystem, ending the period supporting 23 commercial therapies and a record of 788 clinical trials worldwide. Our integrated platform, disciplined execution, and growing utilization of our Global Supply Chain Center Network continue to enhance scalability and operating leverage, advancing our progress toward sustained profitability. This momentum was reflected in our positive adjusted EBITDA of $1.1 million for the quarter, representing another important milestone in our pathway to profitability initiative.

 

“Our strong year-to-date performance, combined with expanding support of commercial therapies, deepening customer relationships, a robust clinical trial pipeline, and continued demand for MVE’s industry-leading products, gives us confidence in our outlook. As a result, we are increasing our full-year 2026 revenue guidance to a range of $197 million to $199 million,” concluded Mr. Shelton.

 

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The following table presents Q3 2026 revenue compared with Q3 2025:

 

Cryoport, Inc. and Subsidiaries

Revenue 

 

   Three Months Ended
September 30,
(unaudited)
   Nine Months Ended
September 30,
(unaudited)
 
(in thousands)  2026   2025   % Change   2026   2025   % Change 
Life Sciences Services  $28,564   $24,258    18%  $83,431   $71,492    17%
BioLogistics Solutions   22,522    19,428    16%   66,549    57,832    15%
BioStorage/BioServices   6,042    4,830    25%   16,882    13,660    24%
Life Sciences Products  $21,656   $19,975    8%  $63,558   $59,235    7%
Total Revenue  $50,220   $44,233    14%  $146,989   $130,727    12%

 

BioLogistics Solutions revenue increased 16% year-over-year in Q3 2026, driven by continued commercial therapies development, and clinical trial progress within the CGT market. BioStorage/BioServices revenue grew 25% year-over-year, reflecting another strong quarter of demand for our expanded, integrated services offering, which provides seamless, secure handling of temperature-sensitive materials across our global network.

 

As of September 30, 2026, the number of commercial cell and gene therapies we support increased to 23 and our total global clinical trial count that we support rose to 788 clinical trials, a net increase of 43 clinical trials over September 30, 2025, with 99 of these clinical trials in Phase 3. The number of trials by phase and region are as follows:

 

Cryoport Supported Clinical Trials by Phase 

 

   September 30, 
Clinical Trials  2024   2025   2026 
Phase 1   295    309    319 
Phase 2   317    353    370 
Phase 3   79    83    99 
Total   691    745   788 

 

Cryoport Supported Clinical Trials by Region

 

   September 30, 
Clinical Trials  2024   2025   2026 
Americas   531    559    589 
EMEA   112    137    143 
APAC   48    49    56 
Total   691    745    788 

 

In Q3 2026, Cryoport’s customer, Replimune, received accelerated U.S. Food and Drug Administration (FDA) approval for TUDRIQEV™ for the treatment of adults with unresectable advanced cutaneous melanoma, a skin cancer that has spread too widely or deeply to be safely or completely removed with surgery. Also, during the quarter Crispr Therapeutics and their partner Vertex Pharmaceuticals received FDA supplemental approval to expand the label of CASGEVY® for treatment of people 2 years of age and older with either Sickle Cell Disease (SCD) or Transfusion-dependent Beta Thalassemia (TDT). CASGEVY is the first approved genetic therapy indicated for children as young as 2 years for both SCD and TDT .

 

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Two of Cryoport’s customers filed Biologics License Applications (BLA) with the FDA in the third quarter and we anticipate another five possible BLA or Marketing Authorization Applications (MAA) in 2026. Cryoport also anticipates two possible additional new therapy approvals (both of which have received Prescription Drug User Fee Act (PDUFA) dates from the FDA for Q4 2026), and one possible additional supplemental approval for geographic expansion from our customer base this year.

 

Operational Milestones

 

·Cryoport Systems initiated BioLogistics services at its new state-of-the-art Global Supply Chain Center located in Santa Ana, California.
   
·Cryoport Systems’ Global Supply Chain Center in Paris, France, received ISO 9001 and ISO 21973 certifications. ISO 21973 certification is the first international standard developed specifically to address the transportation risks associated with human cells for therapeutic use.
   
·CRYOGENE secured new BioStorage and service contracts with customers including Houston Methodist Medical Center, Sonic Clinical Trials, and XenoSTART.

 

Financial Highlights

 

On June 11, 2025, the Company completed the divestiture of its CRYOPDP specialty courier business to DHL Group. The results of CRYOPDP, a former business within Cryoport’s Life Sciences Services segment, are presented as discontinued operations for all periods and are excluded from the non-GAAP financial measures in this release.

 

Revenue

 

·Total revenue for Q3 2026 was $50.2 million, compared to $44.2 million for Q3 2025, a year-over-year increase of 14%, or $6.0 million.

 

oLife Sciences Services revenue for Q3 2026 (representing 57% of our total revenue) was $28.6 million, compared to $24.3 million for Q3 2025, up 18% year-over-year, including BioStorage/BioServices revenue of $6.0 million, up 25% year-over-year.

 

oLife Sciences Products revenue for Q3 2026 (representing 43% of our total revenue) was $21.7 million, compared to $20.0 million for Q3 2025.

 

·Total revenue for 9M 2026 was $147.0 million, compared to $130.7 million for 9M 2025.

 

oLife Sciences Services revenue for 9M 2026 was $83.4 million, compared to $71.5 million for 9M 2025, including BioStorage/BioServices revenue of $16.9 million, compared to $13.7 million for 9M 2025.

 

oLife Sciences Products revenue for 9M 2026 was $63.6 million, compared to $59.2 million for 9M 2025.

 

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Gross Margin

 

·Total gross margin was 47.5% for Q3 2026, compared to 48.2% for Q3 2025.

 

oGross margin for Life Sciences Services was 50.4% for Q3 2026, compared to 49.7% for Q3 2025.

 

oGross margin for Life Sciences Products was 43.6% for Q3 2026, compared to 46.4% for Q3 2025.

 

·Total gross margin was 46.7% for 9M 2026, compared to 46.9% for 9M 2025.

 

oGross margin for Life Sciences Services was 49.7% for 9M 2026, compared to 48.8% for 9M 2025.

 

oGross margin for Life Sciences Products was 42.6% for 9M 2026, compared to 44.6% for 9M 2025.

 

Operating Costs and Expenses

 

·Operating costs and expenses were $32.6 million for Q3 2026, compared to $31.3 million for Q3 2025. Operating costs and expenses were $97.0 million for 9M 2026, compared to $88.1 million for 9M 2025.

 

Loss from Continuing Operations

 

·Loss from continuing operations was $10.9 million for Q3 2026, compared to a loss of $6.7 million for Q3 2025. Loss from continuing operations was $28.5 million for 9M 2026, compared to a loss of $25.4 million for 9M 2025.

 

Net Income (Loss) – including Discontinued Operations

 

·Net loss was $10.9 million for Q3 2026, compared to net loss of $6.9 million for Q3 2025. Net loss for 9M 2026 was $29.7 million, compared to net income of $89.9 million for 9M 2025. Net income for 9M 2025 was primarily driven by the sale of our CRYOPDP specialty courier business during Q2 2025, which contributed $115.4 million, net of taxes, to income from discontinued operations.

 

·Net loss attributable to common stockholders for Q3 2026 was $12.9 million, or $0.25 per share. Net loss attributable to common stockholders for 9M 2026 was $35.7 million, or $0.71 per share. This compares to net loss attributable to common stockholders of $8.9 million, or $0.18 per share, and net income attributable to common stockholders of $83.9 million, or $1.68 per share, for Q3 2025 and 9M 2025, respectively.

 

Adjusted EBITDA from Continuing Operations

 

·Adjusted EBITDA from continuing operations was $1.1 million for Q3 2026, compared to a negative $0.6 million for Q3 2025. Adjusted EBITDA from continuing operations for 9M 2026 was $0.9 million, compared to a negative $4.4 million for 9M 2025.

 

Cash, Cash equivalents, and Short-Term Investments

 

·Cryoport held $393.1 million in cash, cash equivalents, and short-term investments as of September 30, 2026.

 

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Revenue Guidance for Full-Year 2026

 

·The Company is providing updated full-year 2026 revenue guidance in the range of $197 million to $199 million. The Company's 2026 revenue guidance is dependent on its current business and expectations, which may be impacted by, among other things, factors that are outside of our control, such as national economic factors, the global macroeconomic and geopolitical environment, supply chain constraints, inflationary pressures, tariffs and other trade restrictions and/or the effects of foreign currency fluctuations, as well as the other factors described in the Company's filings with the Securities and Exchange Commission ("SEC"), including in the "Risk Factors" section of its most recently filed periodic reports on Form 10-K and Form 10-Q, as well as in its subsequent filings with the SEC.

 

Note: All reconciliations of GAAP to adjusted (non-GAAP) figures above are detailed in the reconciliation tables included later in the press release.

 

Additional Information

 

Further information on Cryoport’s financial results is included in the attached condensed consolidated balance sheets and statements of operations, and additional explanations of Cryoport’s financial performance are provided in the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2026, which is expected to be filed with the Securities and Exchange Commission ("SEC") on November 5, 2026. Additionally, the full report will be available in the SEC Filings section of the Investor Relations section of Cryoport’s website at www.cryoportinc.com.

 

Earnings Conference Call Information

 

IMPORTANT INFORMATION: In addition to the earnings release, a document titled “Cryoport Third Quarter 2026 in Review,” providing a review of Cryoport’s business update, will be issued at 4:05 p.m. ET on Thursday, November 5, 2026. The document is designed to be read in advance of the questions and answers conference call and will be accessible at https://ir.cryoportinc.com/news-events/ir-calendar.

 

Cryoport management will host a conference call at 5:00 p.m. ET on November 5, 2026. The conference call will be in the format of a questions and answers session and will address any queries investors have regarding the Company’s reported results. A slide deck will accompany the call.

 

Conference Call Information

 

Date: Thursday, November 5, 2026
   
Time: 5:00 p.m. ET
   
Dial-in numbers: 1-800-717-1738 (U.S.), 1-646-307-1865 (International)
   
Confirmation code: Request the “Cryoport Call” or Conference ID: 1107312
   
Live webcast:

‘Investor Relations’ section at www.cryoportinc.com or click here.

 

Please allow 10 minutes prior to the call to visit this site to download and install any necessary audio software.

 

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The questions and answers call will be recorded and available approximately three hours after completion of the live event in the Investor Relations section of the Company's website at www.cryoportinc.com for a limited time. To access the replay of the questions and answers click here. A dial-in replay of the call will also be available to those interested, until November 12, 2026. To access the replay, dial 1-844-512-2921 (United States) or 1-412-317-6671 (International) and enter replay entry code: 1107312#.

 

About Cryoport, Inc.

 

Cryoport, Inc. (Nasdaq: CYRX) is a leading global provider of integrated temperature-controlled supply chain solutions for the life sciences, with an emphasis on regenerative medicine. We support biopharmaceutical companies, contract manufacturers (CDMOs), contract research organizations (CROs), developers, and researchers with a comprehensive suite of services and products designed to minimize risk and maximize reliability across the temperature-controlled supply chain for the life sciences. Our integrated supply chain platform includes the Cryoportal® Logistics Management Platform, advanced temperature-controlled packaging, informatics, specialized BioLogistics, BioStorage, BioServices, cryopreservation services, and cryogenic systems, which in varying combinations deliver end-to-end solutions that meet the rigorous demands of the life sciences. With innovation, regulatory compliance, and agility at our core, we are "Enabling the Future of Medicine™." 

 

Headquartered in Nashville, Tennessee, our company maintains a strong global presence with operations across the Americas, EMEA, and APAC.

 

For more information, visit www.cryoportinc.com or follow via LinkedIn at https://www.linkedin.com/company/cryoportinc or @cryoport on X, formerly known as Twitter at https://x.com/cryoport for live updates.

 

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Forward-Looking Statements

 

Statements in this press release which are not purely historical, including statements regarding the Company's intentions, hopes, beliefs, expectations, representations, projections, plans or predictions of the future, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, those related to the Company's industry, business, long-term growth prospects, plans, strategies, acquisitions, future financial results and financial condition, such as the Company's outlook and guidance for full-year 2026 revenue and the related assumptions and factors expected to drive revenue, projected growth trends in the markets in which the Company operates, the Company's plans and expectations regarding the launch of new products and services, such as the expected timing and benefits of such products and services launches, the Company’s expectations about future benefits of its acquisitions, and anticipated regulatory filings, approvals, label/geographic expansions or moves to earlier lines of treatment approved with respect to the products of the Company's clients. Forward-looking statements also include those related to the Company’s plans regarding its Global Supply Chain Centers, including expected timing of future openings, the Company’s anticipation that it will benefit from its operating leverage, the Company’s belief that it is well positioned to further expand margins, enhance operating efficiency and deliver sustainable, profitable long-term growth for its shareholders, and the Company’s expectation that upcoming growth catalysts in its business segments will drive the Company to new heights in market position, growth, and productivity. It is important to note that the Company's actual results could differ materially from those in any such forward-looking statements. Factors that could cause actual results to differ materially include, but are not limited to, risks and uncertainties associated with the effects of changing economic and geopolitical conditions, such as those resulting from the war with Iran, supply chain constraints, inflationary pressures, the effects of foreign currency fluctuations, trends in the products markets, variations in the Company’s cash flow, market acceptance risks, the effects of tariffs and other trade restrictions, and technical development risks. The Company's business could be affected by other factors discussed in the Company's SEC reports, including in the "Risk Factors" section of its most recently filed periodic reports on Form 10-K and Form 10-Q, as well as in its subsequent filings with the SEC. The forward-looking statements contained in this press release speak only as of the date hereof and the Company cautions investors not to place undue reliance on these forward-looking statements. Except as required by law, the Company disclaims any obligation and does not undertake to update or revise any forward-looking statements in this press release.

 

Cryoport Investor Contacts:

Todd Fromer / Scott Eckstein

KCSA Strategic Communications

cryoport@kcsa.com

 

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Cryoport, Inc. and Subsidiaries

Condensed Consolidated Statements of Operations

 

   Three Months Ended
September 30,
(unaudited)
   Nine Months Ended
September 30,
(unaudited)
 
(in thousands, except share and per share data)  2026   2025   2026   2025 
Revenue                
Life Sciences Services revenue  $28,564   $24,258   $83,431   $71,492 
Life Sciences Products revenue   21,656    19,975    63,558    59,235 
Total revenue   50,220    44,233    146,989    130,727 
Cost of revenue:                    
Cost of services revenue   14,181    12,201    41,936    36,570 
Cost of products revenue   12,205    10,707    36,482    32,814 
Total cost of revenue   26,386    22,908    78,418    69,384 
Gross margin   23,834    21,325    68,571    61,343 
Operating costs and expenses:                    
Selling, general and administrative   27,904    26,734    83,535    75,543 
Engineering and development   4,734    4,523    13,493    12,575 
Total operating costs and expenses   32,638    31,257    97,028    88,118 
Loss from operations   (8,804)   (9,932)   (28,457)   (26,775)
Other income (expense):                    
Investment income   3,027    3,402    9,249    6,441 
Interest expense   (517)   (526)   (1,467)   (1,727)
Other income (expense), net   (4,364)   525    (7,057)   (2,714)
Loss before provision for income taxes   (10,658)   (6,531)   (27,732)   (24,775)
Provision for income taxes   (194)   (165)   (807)   (673)
Loss from continuing operations  $(10,852)  $(6,696)  $(28,539)  $(25,448)
Income (loss) from discontinued operations, net   -    (247)   (1,112)   115,393 
Net income (loss)  $(10,852)  $(6,943)  $(29,651)  $89,945 
Paid-in-kind dividend on Series C convertible preferred stock   (2,000)   (2,000)   (6,000)   (6,000)
Net income (loss) attributable to common stockholders  $(12,852)  $(8,943)  $(35,651)  $83,945 
Net income (loss) per share attributable to common stockholders - basic and diluted  $(0.25)  $(0.18)  $(0.71)  $1.68 
Weighted average common shares issued and outstanding - basic and diluted   50,653,987    50,125,268    50,335,554    50,110,450 
                     
Gross margin - Total [%]   47.5%   48.2%   46.7%   46.9%
Gross margin - Services [%]   50.4%   49.7%   49.7%   48.8%
Gross margin - Products [%]   43.6%   46.4%   42.6%   44.6%

 

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Cryoport, Inc. and Subsidiaries

Condensed Consolidated Balance Sheets

 

   September 30,   December 31, 
   2026   2025 
(in thousands)  (unaudited)     
Current assets          
Cash and cash equivalents  $279,179   $250,494 
Short-term investments   113,897    160,714 
Accounts receivable, net   36,004    33,359 
Inventories   22,438    23,188 
Prepaid expenses and other current assets   5,186    8,419 
Total current assets   456,704    476,174 
Property and equipment, net   96,367    85,448 
Operating lease right-of-use assets   39,473    39,720 
Intangible assets, net   133,277    138,082 
Goodwill   22,030    22,400 
Deposits   1,998    2,092 
Deferred tax assets   1,096    1,073 
Total assets  $750,945   $764,989 
           
Current liabilities          
Accounts payable and other accrued expenses  $16,347   $15,283 
Accrued compensation and related expenses   14,731    12,980 
Deferred revenue   1,455    943 
Current portion of operating lease liabilities   4,378    4,133 
Current portion of finance lease liabilities   448    422 
Current portion of convertible senior notes, net   185,986    185,094 
Current portion of notes payable   159    163 
Current portion of contingent consideration   674    - 
Total current liabilities   224,178    219,018 
Notes payable, net   947    1,087 
Operating lease liabilities, net   38,905    39,078 
Finance lease liabilities, net   688    741 
Deferred tax liabilities   1,748    1,354 
Other long-term liabilities   965    444 
Contingent consideration   -    629 
Total liabilities   267,431    262,351 
Total stockholders' equity   483,514    502,638 
Total liabilities and stockholders' equity  $750,945   $764,989 

 

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Note Regarding Use of Non-GAAP Financial Measures

 

To supplement our financial statements, which are presented on the basis of U.S. generally accepted accounting principles (GAAP), the following non-GAAP measure of financial performance as defined in Regulation G of the Securities Exchange Act of 1934 is included in this release: adjusted EBITDA from continuing operations. Non-GAAP financial measures are not calculated in accordance with GAAP, are not based on any comprehensive set of accounting rules or principles and may be different from non-GAAP financial measures presented by other companies. Non-GAAP financial measures, including adjusted EBITDA from continuing operations, should not be considered as a substitute for, or superior to, measures of financial performance prepared in accordance with GAAP.

 

Adjusted EBITDA from continuing operations is defined as loss from continuing operations adjusted for net interest expense, income taxes, depreciation and amortization expense, stock-based compensation expense, acquisition and integration costs, cost reduction initiatives, investment income, unrealized (gain)/loss on investments, foreign currency loss, changes in fair value of contingent consideration and charges or gains resulting from non-recurring events, as applicable.

 

Management believes that adjusted EBITDA from continuing operations provides a useful measure of Cryoport's operating results, a meaningful comparison with historical results and with the results of other companies, and insight into Cryoport's ongoing operating performance. Further, management and the Company’s board of directors utilize adjusted EBITDA from continuing operations to gain a better understanding of Cryoport's comparative operating performance from period to period and as a basis for planning and forecasting future periods. Adjusted EBITDA from continuing operations is also a significant performance measure used by Cryoport in connection with its incentive compensation programs. Management believes adjusted EBITDA from continuing operations, when read in conjunction with Cryoport's GAAP financials, is useful to investors because it provides a basis for meaningful period-to-period comparisons of Cryoport's ongoing operating results, including results of operations, against investor and analyst financial models, helps identify trends in Cryoport's underlying business and in performing related trend analyses, and it provides a better understanding of how management plans and measures Cryoport's underlying business.

 

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Cryoport, Inc. and Subsidiaries

Reconciliation of GAAP loss from continuing operations to adjusted EBITDA

(unaudited)

 

   Three Months Ended
September 30,
   Nine Months Ended
September 30,
 
(in thousands)  2026   2025   2026   2025 
GAAP loss from continuing operations  $(10,852)  $(6,696)  $(28,539)  $(25,448)
Non-GAAP adjustments to loss:                    
Depreciation and amortization expense   6,467    6,415    19,458    18,798 
Acquisition and integration costs   25    38    25    69 
Cost reduction initiatives   857    160    997    642 
Investment income   (3,027)   (3,402)   (9,249)   (6,441)
Unrealized (gain) loss on investments   4,171    (655)   6,064    620 
Foreign currency loss   380    274    1,485    2,521 
Interest expense, net   517    526    1,467    1,727 
Stock-based compensation expense   2,346    2,526    7,143    7,635 
Change in fair value of contingent consideration   25    —    67    (5,178)
Income taxes   194    165    807    673 
Other adjustments   —    —    1,142    — 
Adjusted EBITDA from continuing operations  $1,103   $(649)  $867   $(4,382)

 

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Filing Exhibits & Attachments

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