MaxCyte Reports Third Quarter 2026 Financial Results and Updates Full Year 2026 Total Revenue Guidance

GlobeNewswire | MaxCyte, Inc
Today at 11:01am UTC

Third Quarter and Recent Business Highlights:

  • Reports total revenue of $10.2 million for the third quarter of 2026, including $8.2 million of core revenue and $2.0 million of SPL Program-related revenue
  • Raises Full Year 2026 Total Revenue Guidance to at least $34.5 million, reflecting a projected return to full-year revenue growth
  • In July, MaxCyte announced a strategic, multi-platform technology license partnership with Genentech
  • MaxCyte today announced the proposed acquisition of Akron Bio, a leading supplier of GMP-grade reagents and ancillary materials, expanding its offering across cell therapy manufacturing and nearly doubling revenue

ROCKVILLE, Md., Nov. 10, 2026 (GLOBE NEWSWIRE) -- MaxCyte, Inc. (NASDAQ: MXCT), a leading cell-engineering company providing enabling platform technologies to advance the discovery, development and commercialization of next-generation cell therapeutics, today announced its third quarter ended September 30, 2026 financial results and raised its 2026 total revenue guidance.

“Today, we announced our intention to acquire Akron Bio, a transformational moment for MaxCyte. I believe combining MaxCyte and Akron will expand our commercial opportunity, strengthen our financial profile, and drive long-term value,” said Maher Masoud, President and CEO of MaxCyte. “MaxCyte’s third quarter results reflect the progress that we have made throughout 2026, with approximately 15% year-over-year core revenue growth expected in the second half of this year, exceeding the growth expectations we established at the beginning of 2026. Looking ahead, our SPL partners are at the forefront of cell therapy program development, with more late-stage programs than ever before, including two pivotal trials that could result in approvals as early as next year. Our enterprise pharma partnership is off to a strong start and represents an exciting opportunity to support its advancing cell therapy pipeline. Together, with building adoption in early research, we now have a broad set of solutions at every stage, from discovery through commercialization. We believe we have strong momentum heading into the end of the year and remain committed to executing on our priorities to drive durable long-term growth.”

Third Quarter Financial Results

  • Total revenue of $10.2 million in the third quarter of 2026, an increase of 49% over the third quarter of 2025.
    • Core business revenue of $8.2 million in the third quarter of 2026, an increase of 27% over the third quarter of 2025.
    • Strategic Platform License (SPL) Program-related revenue was $2.0 million for the third quarter of 2026, compared to $0.4 million in the third quarter of 2025.
  • Gross profit for the third quarter of 2026 was $8.5 million (83% gross margin), compared to $5.2 million (77% gross margin) in the third quarter of 2025.
  • Non-GAAP adjusted gross margin was 80% when excluding SPL Program-related revenue and reserves for excess and obsolete inventory, compared to non-GAAP adjusted gross margin of 81% in the third quarter of 2025.
  • Operating expenses for the third quarter of 2026 were $14.5 million, compared to operating expenses of $19.4 million in the third quarter of 2025.
  • Third quarter 2026 net loss was $4.8 million compared to net loss of $12.4 million for the same period in 2025.
  • EBITDA, a non-GAAP measure, was a loss of $5.1 million for the third quarter of 2026, compared to a loss of $13.1 million for the third quarter of 2025; stock-based compensation expense was $1.0 million in the third quarter of 2026 compared to $2.0 million in the third quarter of 2025.
  • Total SPL agreements was 28 as of September 30, 2026, which includes 13 programs currently in the clinic (defined as programs with at least a cleared IND or equivalent) and one commercial program.
  • Total cash, cash equivalents and investments were $132.7 million as of September 30, 2026.

Full Year 2026 Guidance

  • Excluding the impact of the Akron acquisition, full year revenue is now expected to be at least $34.5 million, consisting of:
    • Core revenue of approximately $28 million.
    • SPL Program-related revenue of at least $6.5 million for the year; SPL Program-related revenue guidance includes both revenue of approximately $4 million from milestone payments and at least $2.5 million from commercial royalties.
  • Assuming the close of the Akron acquisition, MaxCyte expects to have approximately $40.0 to $45.0 million in total cash, cash equivalents and investments as of the end of 2026, which accounts for an estimated $105.0 million paid in cash and acquisition deal expenses, along with $22.0 million drawn under the MidCap Financial credit facility financing.
  • On a pro forma basis, excluding the impact of the Akron acquisition and deal-related expenses and other costs related to the Akron acquisition, MaxCyte now expects to end 2026 with approximately $133 million in total cash, cash equivalents and investments, reflecting higher expected revenues and continued management of expenses.

The pro forma amount above is presented solely to provide a comparison, on a consistent basis, to the $132.7 million of total cash, cash equivalents and investments as of September 30, 2026. Because it excludes the cash purchase price, deal-related expenses and other costs related to the Akron acquisition, it is not a forecast of the Company’s actual year-end cash position, and the Company does not expect to hold approximately $133 million of total cash, cash equivalents and investments as of December 31, 2026.

The following tables provide details regarding the sources of our revenue for the periods presented.

 Three Months Ended  
 September 30
(Unaudited)
  
 2026 2025 %
(in thousands, except percentages)       
Instruments$2,779 $1,376 102%
PAs and Consumables 3,092  2,577 20%
Licenses 1,967  1,803 9%
Assay Service 43  248 (83%)
Other 276  402 (31%)
Total Core Revenue$8,157 $6,406 27%
Milestones 1,004  254 295%
Royalties 991  169 486%
Total Revenue$10,152 $6,829 49%
        

Webcast and Conference Call Details

MaxCyte will host a conference call today, November 10, 2026, at 8:30 a.m. Eastern Time. A live and archived webcast of the event will be available on the "Events" section of the MaxCyte website at https://investors.maxcyte.com/. You can access the conference call by dialing (800) 715-9871 within the U.S. or (646) 307-1963 outside the U.S. The conference ID is 1965284.

About MaxCyte

At MaxCyte®, we are committed to building better cells together. As a leading cell engineering company, we are driving the discovery, development and commercialization of next-generation cell therapies. Our best-in-class Flow Electroporation® technology and SeQure™ gene editing risk assessment services enable high-performance cell engineering and rigorous evaluation of editing outcomes, supporting confidence in therapeutic development. Supported by expert scientific, technical and regulatory guidance, our platform empowers researchers to engineer diverse cell types and payloads, accelerating the development of safe and effective treatments for human health. For more than 25 years, we've been advancing cell engineering, shaping the future of medicine. 

Learn more at maxcyte.com and follow us on LinkedIn and Bluesky.

Non-GAAP Financial Measures

This press release contains EBITDA, which is a non-GAAP measure defined as earnings before interest income and expense, taxes, depreciation and amortization. MaxCyte believes that EBITDA provides useful information to management and investors relating to its results of operations. The Company's management uses these non-GAAP measures to compare the Company's performance to that of prior periods for trend analyses, and for budgeting and planning purposes. The Company believes that the use of EBITDA provides an additional tool for investors to use in evaluating ongoing operating results and trends and in comparing the Company's financial measures with other companies, many of which present similar non-GAAP financial measures to investors, and that it allows for greater transparency with respect to key metrics used by management in its financial and operational decision-making.

This press release also contains Non-GAAP Gross Margin, which we define as Gross Margin when excluding SPL program related revenue and reserves for excess and obsolete inventory. The Company believes that the use of Non-GAAP Gross Margin provides an additional tool to investors because it provides consistency and comparability with past financial performance, as Non-GAAP Gross Margin excludes non-core revenues and inventory reserves, which can vary significantly between periods and thus affect comparability.

Management does not consider these Non-GAAP financial measures in isolation or as an alternative to financial measures determined in accordance with GAAP. The principal limitation of these Non-GAAP financial measures is that they exclude significant revenues and expenses that are required by GAAP to be recorded in the Company's financial statements. In order to compensate for these limitations, management presents these Non-GAAP financial measures along with GAAP results. Non-GAAP measures should be considered in addition to results prepared in accordance with GAAP, but should not be considered a substitute for, or superior to, GAAP results. Reconciliation tables of net loss, the most comparable GAAP financial measure, to EBITDA, and Gross Margin, the most comparable GAAP financial measure, to Non-GAAP Gross Margin, are included at the end of this release. MaxCyte urges investors to review the reconciliation and not to rely on any single financial measure to evaluate the Company's business.

Forward-Looking Statements

This press release contains "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements about us and our industry involve substantial known and unknown risks, uncertainties, and assumptions, including those described in Item 1A under the heading "Risk Factors" and elsewhere in our report on Form 10-K, that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations or financial condition, business strategy and plans, customer expectations and objectives of management for future operations, are forward-looking statements. Forward-looking statements include, but are not limited to, statements about possible or future results of operations or financial position. In some cases, you can identify forward-looking statements because they contain words such as "may," "might," "will," "could," "would," "should," "expect," "plan," "anticipate," "intend," "believe," "estimate," "seek," "predict," "future," "project," "potential," "continue," "contemplate," "target," the negative of these words and similar words or expressions. These statements are inherently uncertain, and investors are cautioned not to unduly rely on these statements. The forward-looking statements contained in this press release, include, without limitation, our full year 2026 revenue and cash guidance, expectations regarding core business revenue growth in the second half of 2026, the proposed acquisition of Akron Bio, the benefits of the Akron acquisition, including the revenue base assumptions, statements concerning the following: our expected future growth and success of our business model; the size and growth potential of the markets for our products, and our ability to serve those markets, increase our market share, and achieve and maintain industry leadership; our ability to expand our customer base and enter into additional SPL partnerships; expectations regarding customer-level activities (including the expected advancement of our SPL partners' clinical programs, including Phase 3 trial initiations); our financial performance and capital requirements; the adequacy of our cash resources and availability of financing on commercially reasonable terms; our expectations regarding general market and economic conditions that may impact investor confidence in the biopharmaceutical industry and affect the amount of capital such investors provide to our current and potential partners; and our use of available capital resources.

Risks and uncertainties related to the proposed acquisition of Akron Bio include, but are not limited to, the possibility that various conditions to the consummation of the proposed transaction may not be satisfied or waived; the risk that shareholder litigation in connection with the transaction may result in significant costs of defense, indemnification and liability; that the acquisition may not close on the expected timeline or at all; the significant costs of the acquisition, which have reduced our cash resources and increased our fixed obligations, including $20.0 million of guaranteed deferred payments; dilution to our stockholders from issued shares of common stock; our ability to integrate Akron Bio and realize the anticipated benefits of the acquisition; and risks related to our new indebtedness under our credit facility, including our debt service obligations. These and other risks and uncertainties are described in greater detail in Item 1A, entitled "Risk Factors," in our Annual Report on Form 10-K for the year ended December 31, 2025, filed with the Securities and Exchange Commission, as well as in discussions of potential risks, uncertainties, and other important factors in the other filings that we make with the Securities and Exchange Commission from time to time. These documents are available through the Investor Menu, Financials section, under "SEC Filings" on the Investors page of our website at http://investors.maxcyte.com. Any forward-looking statements in this press release are based on our current beliefs and opinions on the relevant subject based on information available to us as of the date of such press release, and you should not rely on forward-looking statements as predictions of future events. We undertake no obligation to update any forward-looking statements made in this press release to reflect events or circumstances after the date of this press release or to reflect new information or the occurrence of unanticipated events, except as required by law.

MaxCyte Contacts:

US IR Adviser
Gilmartin Group
Erik Abdow
ir@maxcyte.com

Media Contact
Oak Street Communications
Kristen White
kristen@oakstreetcommunications.com
415.608.6060

MaxCyte, Inc.
Unaudited Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)
     
  September 30, December 31,
  2026
 2025
Assets      
Current assets:      
Cash and cash equivalents $13,372  $20,065 
Short-term investments, at amortized cost  87,908   82,979 
Accounts receivable, net  12,054   3,503 
Inventory, net  7,380   7,547 
Prepaid expenses and other current assets  3,777   4,275 
Assets held for sale  180   — 
Total current assets  124,671   118,369 
       
Investments, non-current, at amortized cost  31,469   52,570 
Property and equipment, net  14,342   17,531 
Right-of-use asset - operating leases  10,237   10,920 
Intangible assets, net  749   650 
Other assets  1,015   2,467 
Total assets $182,483  $202,507 
       
Liabilities and stockholders’ equity      
Current liabilities:      
Accounts payable $1,026  $1,401 
Accrued expenses and other  5,937   7,812 
Operating lease liability, current  1,565   1,456 
Deferred revenue, current portion  7,388   3,598 
Total current liabilities  15,916   14,267 
       
Operating lease liability, net of current portion  15,325   16,487 
Other liabilities  311   263 
Total liabilities  31,552   31,017 
       
Commitments and contingencies      
Stockholders’ equity:      
Preferred stock, $0.01 par value; 5,000,000 shares authorized and no shares issued and outstanding at September 30, 2026 and December 31, 2025     — 
Common stock, $0.01 par value; 400,000,000 shares authorized, 107,493,772 and 106,789,618 shares issued, and 103,233,238 and 106,789,618 outstanding at September 30, 2026 and December 31, 2025, respectively  1,075   1,068 
Additional paid-in capital  435,225   431,905 
Treasury stock, 4,260,534 shares, at cost  (5,500)  — 
Accumulated deficit  (279,869)  (261,483)
Total stockholders’ equity  150,931   171,490 
Total liabilities and stockholders’ equity $182,483  $202,507 
         


MaxCyte, Inc.
Unaudited Condensed Consolidated Statements of Operations
(in thousands, except share and per share amounts)
     
  Three Months Ended
September 30,
 Nine Months Ended
September 30,
  2026
 2025
 2026
 2025
Revenue $10,152  $6,829  $27,074  $25,726 
Cost of goods sold  1,684   1,596   4,928   4,612 
Gross profit  8,468   5,233   22,146   21,114 
             
Operating expenses:            
Research and development  2,874   5,316   10,984   17,488 
Sales and marketing  4,214   3,936   11,006   15,420 
General and administrative  6,553   6,028   19,777   22,634 
Restructuring expense  -   3,058   -   3,058 
Depreciation and amortization  868   1,044   2,837   3,185 
Total operating expenses  14,509   19,382   44,604   61,785 
Operating loss  (6,041)  (14,149)  (22,458)  (40,671)
             
Other income:            
Interest income  1,279   1,733   4,072   5,637 
Total other income  1,279   1,733   4,072   5,637 
Loss before income taxes  (4,762)  (12,416)  (18,386)  (35,034)
Provision for income taxes  —   —   —   — 
Net loss  (4,762)  (12,416)  (18,386)  (35,034)
Other comprehensive income  —   —   —   — 
Comprehensive loss $(4,762) $(12,416) $(18,386) $(35,034)
Basic and diluted net loss per share $(0.05) $(0.12) $(0.17) $(0.33)
Weighted-average shares outstanding, basic and diluted  103,537,926   106,613,075   105,732,991   106,324,792 
                 


MaxCyte, Inc.
Unaudited Condensed Consolidated Statements of Cash Flows
(in thousands)
   
  Nine Months Ended
September 30,
  2026
 2025
Cash flows from operating activities:      
Net loss $(18,386) $(35,034)
       
Adjustments to reconcile net loss to net cash used in operating activities:      
Depreciation and amortization  2,925   3,268 
Impairment of fixed assets  630   — 
Lease right-of-use asset amortization  683   587 
Net book value of consigned equipment sold  105   70 
Loss on disposal of property and equipment  23   132 
Stock-based compensation  3,264   8,507 
Credit loss expense  —   29 
Provision for inventory reserve  400   525 
Amortization of discounts on investments  (1,251)  (2,219)
       
Changes in operating assets and liabilities, net of effects of acquisition:      
Accounts receivable  (8,551)  (3,649)
Inventory  (708)  647 
Prepaid expense and other current assets  498   744 
Other assets  1,464   (924)
Accounts payable, accrued expenses and other  (2,217)  (3,338)
Operating lease liability  (1,053)  (939)
Deferred revenue  3,790   (80)
Other liabilities  48   (47)
Net cash used in operating activities  (18,336)  (31,721)
       
Cash flows from investing activities:      
Purchases of investments  (55,113)  (98,031)
Maturities of investments  72,536   117,600 
Purchases of property and equipment  (193)  (1,537)
Acquisition of intangible assets  (150)  — 
Acquisition of business, net of cash acquired of $541  —   (1,773)
Net cash provided by investing activities  17,080   16,259 
       
Cash flows from financing activities:      
Proceeds from exercise of stock options  29   417 
Proceeds from issuance of common stock under employee stock purchase plan  34   134 
Repurchases of common stock  (5,500)  — 
Net cash (used in) provided by financing activities  (5,437)  551 
Net decrease in cash and cash equivalents  (6,693)  (14,911)
Cash and cash equivalents, beginning of period  20,065   27,884 
Cash and cash equivalents, end of period $13,372  $12,973 
         


 
     
     
         
                 
                 
                 
                 
                 
Unaudited Reconciliation of Net Loss to EBITDA
(in thousands)
(Unaudited)
 
     
     
         
                 
                 
                 
                 
                 
     
 
     
     
         
                 
                 
                 
                 
                 
  Three Months Ended
September 30,
 Nine Months Ended
September 30,
 
     
     
         
                 
                 
                 
                 
                 
  2026
 2025
 2026
 2025
 
     
     
         
                 
                 
                 
                 
                 
Net loss $(4,762) $(12,416) $(18,386) $(35,034)
 
     
     
         
                 
                 
                 
                 
                 
Depreciation and amortization expense  900   1,072   2,925   3,268 
 
     
     
         
                 
                 
                 
                 
                 
Interest income  (1,279)  (1,733)  (4,072)  (5,637)
 
     
     
         
                 
                 
                 
                 
                 
Income taxes  —   —   —   — 
 
     
     
         
                 
                 
                 
                 
                 
EBITDA $(5,141) $(13,077) $(19,533) $(37,403)
                 


Unaudited Reconciliation of Gross Margin to Non-GAAP Adjusted Gross Margin
(in thousands, except for percentages)
(Unaudited)
    
 Three months ended September 30, 2026 Three months ended September 30, 2025
 GAAP Adjustments Non-GAAP GAAP Adjustments Non-GAAP
Revenue$10,152  $(1,995) $8,157  $6,829  $(423) $6,406 
Cost of Goods Sold 1,684   (21)  1,663   1,596   (360)  1,236 
Gross Margin$8,468  $(1,974) $6,494  $5,233  $(63) $5,170 
Gross Margin % 83%    80%  77%    81%


 Nine months ended September 30, 2026 Nine months ended September 30, 2025
 GAAP Adjustments Non-GAAP GAAP Adjustments Non-GAAP
Revenue$27,074  $(6,197) $20,877  $25,726  $(2,878) $22,848 
Cost of Goods Sold 4,928   (400)  4,528   4,612   (525)  4,087 
Gross Margin$22,146  $(5,797) $16,349  $21,114  $(2,353) $18,761 
Gross Margin % 82%    78%  82%    82%
                    
(1) Adjustments include the exclusion of SPL program related revenue from Revenue, and the exclusion of reserves for excess and obsolete inventory from Cost of Goods Sold.




Primary Logo