Codexis (CDXS) risk factors, FY2025 10-K

Codexis's FY2025 10-K, filed Mar 11, 2026, lists 44 risk factors in 4 groups. Against the prior year's 43: 5 new, 4 dropped, 7 substantially reworded.

Risk factors listed
444 groups
New this year
5vs 43 last year
Dropped
4since the prior 10-K
Substantially reworded
7of those kept
Section length
21k wordsItem 1A

What the changes say

  • Accumulated deficit reached $606.8 million after a $44.0 million net loss in 2025.
  • Manufacturing relies heavily on specific third-party CMOs abroad.
  • Concentration of revenue remains high at 51% from key customers.

What changed since the prior 10-K

New

  • NewRisks Related to Our Business and Strategy

    We are dependent on a limited number of third-party contract manufacturers for large scale production of substantially all of our enzymes

    We depend on third-party contract manufacturers like Lactosan, ACS Dobfar, and Sekisui Diagnostics for large-scale enzyme production due to limited internal capacity.

  • NewRisks Related to Our Business and Strategy

    Finally, our business could be negatively affected if any of our collaborators or suppliers undergoes a change of control or were to otherwise assign the rights or obligations under any of our agreements

    Changes of control at our collaborators or suppliers could negatively impact our business and our ECO Synthesis platform.

  • NewRisks Related to Our Business and Strategy

    We have made acquisitions in the past, and if appropriate opportunities become available, we may acquire additional businesses, assets, technologies, or products to enhance our business in the future

    Future business acquisitions could dilute stockholders, incur debt, or cause integration and management challenges.

  • NewRisks Related to Owning our Common Stock

    International trade policies, including tariffs, sanctions and trade barriers, may adversely affect our business

    International tariffs, trade policies, and sanctions could increase operating costs and disrupt our global supply chain.

  • NewRisks Related to Owning our Common Stock

    Our business may be affected by the evolving regulatory framework for AI Technologies

    Our use of AI, machine learning, and automated decision-making technologies introduces new regulatory, cybersecurity, and operational risks.

Dropped

  • DroppedRisks Related to Our Business and Strategy

    Even after collaboration relationships expire or terminate, some elements of the collaboration may survive. For instance, certain rights, licenses and obligations of each party with respect to intellectual property and program materials may survive the expiration or termination of the collaboration

  • DroppedRisks Related to Our Business and Strategy

    We have invested significant resources to enable enzymatic nucleic acid synthesis, which is based on novel ideas and technologies that are largely unproven

  • DroppedRisks Related to Our Business and Strategy

    We have investments in non-marketable securities, which may subject us to significant impairment charges

  • DroppedRisks Related to Our Business and Strategy

    If we engage in any acquisitions, we will incur a variety of costs and may potentially face numerous risks that could adversely affect our business and operations

Reworded

  • 79% rewrittenRisks Related to Our Business and Strategy

    Any productivity issues or higher-than-expected costs at our facilities could result in material and adverse impacts on our financial condition and results of operations

    Text remains identical to the prior year.

  • 76% rewrittenRisks Related to Our Business and Strategy

    We may receive limited revenue or no future value from certain of our existing license agreements

    Removed specific references to Nestlé and CDX-7108, generalizing uncertainty on whether terminated biotherapeutic license agreements will yield future value.

    Was: Given our change in strategic direction, we may receive limited revenue or no future value from certain of our existing license agreements

  • 34% rewrittenRisks Related to Our Business and Strategy

    We believe that our products are exempt from FDCA requirements, but FDA or other regulators may disagree and find that our products are subject to such requirements

    Clarified that products are not incorporated into final products by customers and updated references to multiple CDMO collaborations for siRNA.

  • 29% rewrittenRisks Related to Owning our Common Stock

    Actual or perceived failures to comply with applicable data protection, privacy and security laws, regulations, standards and other requirements could adversely affect our business, results of operations and financial condition

    Text remains identical to the prior year.

  • 27% rewrittenRisks Related to Our Business and Strategy

    We have a history of net losses and we may not achieve or maintain profitability

    Updated financial figures for fiscal year 2025, reporting a net loss of $44.0 million and an accumulated deficit of $606.8 million.

  • 26% rewrittenRisks Related to Our Business and Strategy

    We are dependent on a limited number of customers

    Updated revenue concentration figures to show key customers accounted for 51% of total revenues in both 2025 and 2024.

  • 23% rewrittenRisks Related to Intellectual Property

    Litigation may be necessary to enforce our intellectual property rights, to protect our trade secrets, to determine the validity and scope of the proprietary rights of others, or to defend against claims of infringement, invalidity, misappropriation, or other claims

    Added a hedge noting that any required licenses resulting from IP litigation may be on unfavorable terms.

All 44 risk factors

Headings as the filing states them, in filing order.

Risks Related to Our Business and Strategy

  1. 01We have a history of net losses and we may not achieve or maintain profitability27% rewritten
  2. 02We believe that our products are exempt from FDCA requirements, but FDA or other regulators may disagree and find that our products are subject to such requirements34% rewritten
  3. 03We are dependent on a limited number of customers26% rewritten
  4. 04Some of our product supply agreements with customers, if in place, have finite duration, may not be extended or renewed and generally do not require the customer to purchase any particular quantity or quantities of our products
  5. 05If we are unable to develop and commercialize new products for the pharmaceutical and life science tools markets, our business and prospects will be harmed
  6. 06A reduction or delay in government funding of research and development for our customers may adversely affect our business
  7. 07The services and offerings we provide are highly complex, and if we encounter problems providing the services or support required, our business could suffer
  8. 08Any productivity issues or higher-than-expected costs at our facilities could result in material and adverse impacts on our financial condition and results of operations79% rewritten
  9. 09We are dependent on a limited number of third-party contract manufacturers for large scale production of substantially all of our enzymesNew
  10. 10We are dependent on our collaborators, and our failure to successfully manage these relationships could prevent us from developing and commercializing many of our products and achieving or sustaining profitability
  11. 11Finally, our business could be negatively affected if any of our collaborators or suppliers undergoes a change of control or were to otherwise assign the rights or obligations under any of our agreementsNew
  12. 12Competitors and potential competitors who have greater resources and experience than we do may develop products and technologies that make ours obsolete or may use their greater resources to gain market share at our expense
  13. 13Ethical, legal and social concerns about genetically engineered products and processes could limit or prevent the use of our technology, products and processes and limit our revenues
  14. 14As a result of our refined focus on certain programs and business lines, we may fail to capitalize on other opportunities that may be more profitable or for which there is a greater likelihood of success
  15. 15We may receive limited revenue or no future value from certain of our existing license agreements76% rewritten
  16. 16The timing of our customer orders and related product revenue recognition is unpredictable and may cause our operating results to vary significantly from quarter to quarter, which could adversely affect our stock price
  17. 17Our ability to use our net operating loss carryforwards to offset future taxable income may be subject to certain limitations
  18. 18We may need additional capital in the future in order to expand our business
  19. 19We have made acquisitions in the past, and if appropriate opportunities become available, we may acquire additional businesses, assets, technologies, or products to enhance our business in the futureNew

Risks Related to Government Regulation

  1. 20Even if our customers, future customers or collaborators obtain regulatory approval for any products utilizing our enzymes, such products will remain subject to ongoing regulatory requirements, which may result in significant additional expense
  2. 21If we or our customers fail to comply with certain healthcare laws, including fraud and abuse laws, we could face substantial penalties and our business, results of operations, financial condition and prospects could be adversely affected
  3. 22Ongoing healthcare legislative and regulatory reform measures may have a material adverse effect on our business and results of operations
  4. 23Compliance with European Union chemical regulations could be costly and adversely affect our business and results of operations
  5. 24The biopharmaceutical industry is subject to extensive regulatory obligations and policies that may be subject to significant and abrupt change, including due to judicial challenges, election cycles, and resulting regulatory updates and changes in policy priorities

Risks Related to Intellectual Property

  1. 25Our efforts to prosecute, maintain, protect and/or defend our intellectual property rights may not be successful
  2. 26Litigation may be necessary to enforce our intellectual property rights, to protect our trade secrets, to determine the validity and scope of the proprietary rights of others, or to defend against claims of infringement, invalidity, misappropriation, or other claims23% rewritten
  3. 27Our ability to compete may decline if we do not adequately prosecute, maintain, protect and/or defend our proprietary technology, products or services or our intellectual property rights
  4. 28Third parties may claim that we are infringing, violating or misappropriating their intellectual property rights, which may subject us to costly and time-consuming litigation and prevent us from developing or commercializing our technology, products or services
  5. 29We may be involved in lawsuits to protect or enforce our intellectual property rights, which could be expensive, time-consuming and unsuccessful
  6. 30We may not be able to enforce our intellectual property rights throughout the world
  7. 31If our biocatalysts, or the genes that code for our biocatalysts, are stolen, misappropriated or reverse engineered, others could use these biocatalysts or genes to produce competing products
  8. 32Confidentiality and non-use agreements with employees, consultants, advisors and other third parties may not adequately prevent disclosures and non-use of trade secrets and other proprietary information

Risks Related to Owning our Common Stock

  1. 33We are subject to anti-takeover provisions in our certificate of incorporation and bylaws and under Delaware law that could delay or prevent an acquisition of our company, even if the acquisition would be beneficial to our stockholders
  2. 34Our quarterly or annual operating results may fluctuate in the future. As a result, we may fail to meet or exceed the expectations of research analysts or investors, which could cause our stock price to decline
  3. 35We do not intend to pay cash dividends for the foreseeable future
  4. 36If securities or industry analysts do not publish research or reports about our business, or publish negative reports about our business, our stock price and trading volume could decline
  5. 37We face risks associated with our international business
  6. 38Market and economic conditions may negatively impact our business, financial condition, and share price
  7. 39International trade policies, including tariffs, sanctions and trade barriers, may adversely affect our businessNew
  8. 40Business interruptions resulting from disasters or other disturbances could delay us in the process of developing our products and could disrupt our sales. Our business continuity and disaster recovery plans may not adequately protect us from a serious disaster or other disturbance
  9. 41Actual or perceived failures to comply with applicable data protection, privacy and security laws, regulations, standards and other requirements could adversely affect our business, results of operations and financial condition29% rewritten
  10. 42As we continue to expand into other foreign countries and jurisdictions, we may be subject to additional laws and regulations that may affect how we conduct business
  11. 43Our business may be affected by the evolving regulatory framework for AI TechnologiesNew
  12. 44Evolving expectations around corporate responsibility practices, specifically related to environmental, social and governance (“ESG”) matters, may expose us to reputational and other risks

Other Codexis 10-Ks

  • FY2024 10-K risk factors
    43 risks

    Codexis faces significant ongoing net losses with an accumulated deficit of $562.8 million as of December 31, 2024. Revenue is heavily concentrated, with customers contributing 10% or more accounting for 51% of total revenue in 2024. The company relies heavily on unproven novel technologies like the ECO Synthesis manufacturing platform for enzymatic nucleic acid synthesis.

    Filed Feb 27, 2025

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.