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Codexis Reports Fourth Quarter and Fiscal Year 2025 Financial Results

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Codexis (NASDAQ: CDXS) reported fourth-quarter revenue of $38.9M and fiscal 2025 total revenue of $70.4M. The company ended 2025 with $78.2M in cash and expects runway through 2027. Fiscal 2025 saw product gross margin of 64% and a net loss of $44.0M.

Q4 growth was driven by a $37.8M Technology Transfer Agreement with Merck and momentum in ECO Synthesis commercial engagements; the company provided 2026 revenue guidance of $72M–$76M.

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Positive

  • Total revenue +19% to $70.4M in fiscal 2025
  • Product gross margin improved to 64% for fiscal 2025
  • Signed $37.8M Merck technology transfer agreement in Q4 2025

Negative

  • Net loss of $44.0M for fiscal 2025
  • R&D spend increased to $52.3M, up from $46.3M
  • One-time restructuring charge of $3.4M in fiscal 2025

Market Reaction – CDXS

+40.95% $1.79 3.3x vol
15m delay 31 alerts
+40.95% Since News
+49.1% Peak in 1 hr 31 min
$1.79 Last Price
$1.18 $2.00 Day Range
+$33M Valuation Impact
$115M Market Cap
3.3x Rel. Volume

Following this news, CDXS has gained 40.95%, reflecting a significant positive market reaction. Argus tracked a peak move of +49.1% during the session. Our momentum scanner has triggered 31 alerts so far, indicating elevated trading interest and price volatility. The stock is currently trading at $1.79. This price movement has added approximately $33M to the company's valuation. Trading volume is very high at 3.3x the average, suggesting strong buying interest.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Silver for real-time data.

Key Figures

Q4 2025 revenue: $38.9 million FY 2025 revenue: $70.4 million Cash & investments: $78.2 million +5 more
8 metrics
Q4 2025 revenue $38.9 million Fourth quarter 2025 total revenues, up from $21.5 million in Q4 2024
FY 2025 revenue $70.4 million Fiscal year 2025 total revenue, a 19% increase vs. $59.3 million in 2024
Cash & investments $78.2 million Cash, cash equivalents and short-term investments as of December 31, 2025
Merck agreement $37.8 million Technology Transfer Agreement completed with Merck in Q4 2025
FY 2025 product margin 64% Product gross margin for fiscal 2025 vs. 56% in fiscal 2024
FY 2025 net loss $44.0 million ($0.50/share) Net loss for fiscal 2025 vs. $65.3 million ($0.89/share) in 2024
Q4 2025 net income $9.6 million ($0.11/share) Fourth quarter 2025 net income vs. $10.4 million net loss in Q4 2024
2026 revenue guidance $72–76 million Total revenue outlook for 2026 provided in this release

Market Reality Check

Price: $1.27 Vol: Volume 0.92M is below the...
low vol
$1.27 Last Close
Volume Volume 0.92M is below the 20-day average of 1.61M, suggesting muted positioning into earnings. low
Technical Shares at 1.24 are trading below the 200-day MA of 2.15, reflecting a longer-term downtrend into this report.

Peers on Argus

CDXS was down 0.8% while several biotech peers were positive, including OABI up ...

CDXS was down 0.8% while several biotech peers were positive, including OABI up 2.05%, SLN up 2.12%, ACIU up 5.56%, and VOR up 3.96%; only PRQR fell 4.26%, pointing to more company‑specific dynamics.

Previous Earnings Reports

5 past events · Latest: Nov 06 (Negative)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 06 Q3 2025 earnings Negative -16.9% Weaker revenue, restructuring, workforce reductions and large quarterly net loss.
Aug 13 Q2 2025 earnings Positive +1.6% Revenue beat, higher margins and strengthened cash via ATM and loan.
May 14 Q1 2025 earnings Negative +1.6% Revenue decline and wider net loss despite first ECO Synthesis contract.
Feb 27 FY 2024 results Neutral -22.6% Slight revenue decline but improved loss and detailed 2025 guidance.
Oct 31 Q3 2024 earnings Positive +11.5% Revenue growth, narrowed loss and extended cash runway into 2027.
Pattern Detected

Earnings days have often been volatile, with several past reports followed by double‑digit percentage moves, skewed modestly negative on average.

Recent Company History

Across recent earnings reports from October 2024 through November 2025, Codexis has mixed financial trends but consistent focus on extending cash runway and scaling its ECO Synthesis platform. Prior updates included revenue growth phases, cost restructuring, workforce reductions, and external partnerships such as Merck. Price reactions have ranged from strong rallies to sharp selloffs, and the average move around these earnings events has been negative, highlighting how results and outlook commentary have materially influenced sentiment.

Historical Comparison

-5.0% avg move · In the last five earnings reports, CDXS saw an average move of -4.98%, with reactions ranging from s...
earnings
-5.0%
Average Historical Move earnings

In the last five earnings reports, CDXS saw an average move of -4.98%, with reactions ranging from strong rallies to sharp selloffs, underscoring how sensitive the stock has been to financial updates and guidance shifts.

Earnings updates have traced Codexis’s shift from revenue volatility and sizable losses toward improved margins, runway extension into 2027, and growing ECO Synthesis commercialization, often accompanied by financing or restructuring actions.

Market Pulse Summary

The stock is surging +41.0% following this news. A strong positive reaction aligns with the improvem...
Analysis

The stock is surging +41.0% following this news. A strong positive reaction aligns with the improvement in Codexis’s fundamentals highlighted here, including FY 2025 revenue rising to $70.4 million, higher product margins of 64%, and a swing to $9.6 million Q4 net income. Historically, earnings days have averaged a -4.98% move, so a sharp upside response would represent a break from that pattern. Investors could weigh sustainability against prior financing actions and ongoing net losses on a full‑year basis.

Key Terms

ECO Synthesis, siRNA, CDMO, GMP, +4 more
8 terms
ECO Synthesis technical
"importance of our ECO Synthesis® Manufacturing Platform to customers in the RNAi industry"
Eco synthesis is the development or use of chemical and manufacturing methods designed to minimize environmental harm and resource use while making a product. Think of it like switching from a dirty, wasteful factory line to a cleaner, more efficient one: it can lower long‑term costs, reduce regulatory and reputational risks, and open products to buyers who prefer sustainable options, all of which matter to investors evaluating future profitability and risk.
siRNA medical
"producing a 10 g siRNA batch utilizing our fully enzymatic synthesis process"
Small interfering RNA (siRNA) is a short strand of genetic material that binds to and destroys the messenger RNA that carries instructions for making a specific protein, effectively switching that gene off. Investors care because siRNA is a platform for precise medicines: successful trials or approvals can create high-value drugs, while delivery challenges, manufacturing complexity, patent positions and regulatory risk can sharply affect a biotech company's prospects.
CDMO technical
"contracts with leading pharma, high growth biotech, and top tier CDMOs"
A contract development and manufacturing organization (CDMO) is a company that provides specialized services to help develop and produce pharmaceutical products for other businesses. Think of it as a contract factory that takes a company's recipe and makes the product on their behalf. For investors, CDMOs are important because they support the growth of pharmaceutical companies and can be key partners in bringing new medicines to market.
GMP technical
"Signed a lease on our GMP facility, which, once operational, will be capable of kilogram scale"
Good Manufacturing Practice (GMP) is a set of regulatory standards and procedures that ensure products—especially medicines, medical devices, and related goods—are consistently made to meet safety, quality, and purity requirements. For investors, GMP compliance is like a factory’s hygiene and checklist system: it reduces the risk of product recalls, regulatory fines, and production stoppages, supports market access, and signals more reliable, lower-risk operations that can protect revenue and reputation.
ISO 9001 technical
"Received ISO 9001 certification of our in-house manufacturing suite"
ISO 9001 is an international standard for a company’s quality management system that sets out how the organization documents and controls its processes to deliver consistent products or services. For investors, certification is like a stamp saying the company follows repeatable, audited procedures—this can lower operational risk, improve efficiency and customer trust, and make performance more predictable over time.
IND-enabling studies regulatory
"support customer assets that are moving into preclinical and IND-enabling studies"
Ind-enabling studies are early research efforts that test whether a new drug or treatment is safe and effective enough to move forward in development. They are like preliminary tests to ensure a product works as intended before investing more resources into large-scale trials. For investors, these studies are important because successful results can signal potential progress toward bringing a new product to market, impacting its future value.
FDA Emerging Technologies regulatory
"Continue our engagement with FDA Emerging Technologies team to discuss ECO synthesis-derived siRNA"
The FDA Emerging Technologies program is a pathway through the U.S. regulatory agency that gives early, technical feedback to companies deploying new manufacturing methods, materials, or digital tools for drugs, biologics, and medical devices. For investors, participation can reduce regulatory surprises and speed reliable production—think of it as getting a pre-launch check from the regulator that can lower time, cost and risk associated with bringing innovative products to market.
stereoisomer medical
"groundbreaking work on stereoisomer control at TIDES US, which showed that ECO Synthesis"
A stereoisomer is one of two or more molecules that have the same atoms and bonds but differ in the three-dimensional arrangement of those atoms, like left and right hands that are mirror images. For investors, stereoisomers matter because different arrangements can change a drug’s effectiveness, side effects, regulatory approval, manufacturing complexity and patent protection, all of which can affect a company’s sales, costs and legal risks.

AI-generated analysis. Not financial advice.

     Q4 revenue of $38.9 million, total revenue of $70.4 million for the fiscal year ended December 31, 2025

Ended year with $78.2 million in cash, cash equivalents and short-term investments, runway through 2027

Completed $37.8 million Technology Transfer Agreement with Merck

REDWOOD CITY, Calif., March 11, 2026 (GLOBE NEWSWIRE) -- Codexis, Inc. (NASDAQ: CDXS), a leading provider of enzymatic solutions for efficient and scalable manufacturing of complex therapeutics, today announced financial results for the fourth quarter and year ended December 31, 2025, and provided a business update.

“Throughout 2025, we made significant strides in demonstrating the importance of our ECO Synthesis® Manufacturing Platform to customers in the RNAi industry. We’ve secured multiple contracts with leading pharma, high growth biotech, and top tier CDMOs, underscoring the commercial potential of our platform,” said Alison Moore, PhD, President and Chief Executive Officer at Codexis. “We achieved many technological advancements this year, including producing a 10 g siRNA batch utilizing our fully enzymatic synthesis process, as well as a 3 kg siRNA batch from one of our customers utilizing our ligase product. As we look to the year ahead, we are focused on demonstrating the value of our technology to our customers through expanded partnerships, and continuing our history of innovation in oligonucleotide manufacturing.”

Recent Business Highlights

  • Engaging with over 40 companies on 55 potential opportunities, including existing and new customers. Our conversations throughout 2025 have evolved from feasibility testing to discussions around contracts with broader scope activities that support customer assets that are moving into preclinical and IND-enabling studies.
  • Signed a lease on our GMP facility, which, once operational, will be capable of kilogram scale manufacturing utilizing our ECO Synthesis platform.
  • Signed an agreement with Axolabs, our third CDMO partnership, to evaluate our ECO Synthesis technology for integration into their manufacturing site.
  • Unveiled groundbreaking work on stereoisomer control at TIDES US, which showed that ECO Synthesis can deliver defined stereochemistry in oligonucleotide products, potentially benefiting therapeutic potency.
  • Received ISO 9001 certification of our in-house manufacturing suite and successfully completed a pharmaceutical partner audit in support of future commercial contracts.
  • Preparing to support commercial launch of 2 (two) pharma biocatalysis products following successful phase 3 data.

Upcoming Milestones

  • Advance our partnerships with drug innovators toward clinical stage manufacturing agreements.
  • Expand our relationships with our CDMO partners, commencing a strategic partnership with a goal of at least one by the end of 2026.
  • Seeking to sign a licensing deal with a major pharmaceutical company in the second half of 2026.
  • We anticipate hosting presentations at the 2026 TIDES USA annual meeting, where we plan to present data on specific stereoisomer configurations uniquely delivered via enzymatic synthesis.
  • Continue our engagement with FDA Emerging Technologies team to discuss ECO synthesis-derived siRNA product quality, stereoisomer control, and product comparability.
  • We expect to begin retrofit construction on our GMP facility in the second half of 2026 with the facility in full production capability by the end of 2027.

Fiscal Year 2025 Financial Highlights

  • Total revenues increased by 19% to $70.4 million for fiscal year 2025 compared to $59.3 million for fiscal year 2024. The increase was primarily due to the Merck Technology Transfer Agreement executed in the fourth quarter of 2025, higher revenue from legacy and existing agreements, partially offset by variability in customers’ manufacturing schedules and clinical trial progression.
  • Product gross margin was 64% for fiscal year 2025 compared to 56% for fiscal year 2024. The increase in gross margin was largely due to a shift in sales toward more profitable products, and declines in less profitable, legacy products.
  • Research & Development expenses for fiscal year 2025 were $52.3 million compared to $46.3 million for fiscal year 2024. The increase was primarily driven by an increase in employee-related costs, higher lab supplies expense, higher allocable costs, partially offset by a decrease in outside services related to manufacturing and regulatory expense.
  • Selling, General & Administrative expenses for fiscal year 2025 were $47.1 million compared to $55.1 million for fiscal year 2024. The decrease was primarily due to lower stock-based compensation expenses, lower legal expenses and reduced use of outside services.
  • Fiscal 2025 expenses also included one-time restructuring charges of $3.4 million related to the reduction in force announced in November 2025.
  • The net loss for fiscal year 2025 was $44.0 million, or $0.50 per share, compared to a net loss of $65.3 million, or $0.89 per share, for fiscal year 2024.
  • As of December 31, 2025, the Company had $78.2 million in cash, cash equivalents and short-term investments.

Fourth Quarter 2025 Financial Highlights

  • Total revenues increased by 81% to $38.9 million for the fourth quarter of 2025 compared to $21.5 million in the fourth quarter of 2024. The increase was primarily due to the Merck Technology Transfer Agreement executed in the fourth quarter of 2025, partially offset by variability in customers’ manufacturing schedules and clinical trial progression.
  • Product gross margin was 65% for the fourth quarter of 2025 compared to 63% in the fourth quarter of 2024. The increase in gross margin was largely due to a shift in sales toward more profitable products, and declines in less profitable, legacy products.
  • Research & Development expenses for the fourth quarter of 2025 were $11.7 million compared to $12.1 million in the fourth quarter of 2024. The decrease was primarily driven by lower employee-related costs and lower stock-based compensation expenses.
  • Selling, General & Administrative expenses for the fourth quarter of 2025 were $11.2 million compared to $13.0 million in the fourth quarter of 2024. The decrease was primarily due to lower employee-related costs and reduced use of outside services.
  • Fourth quarter 2025 expenses also included one-time restructuring charges of $3.4 million related to the reduction in force announced in November 2025.
  • The net income for the fourth quarter of 2025 was $9.6 million, or $0.11 per share, compared to a net loss of $10.4 million, or $0.13 per share, for the fourth quarter of 2024.

2026 Financial Guidance

We are introducing financial guidance for 2026, as follows:

  • Total revenues are expected to be in the range of $72 million to $76 million.
  • We expect our existing cash, cash equivalents and short-term investments will be sufficient to fund our planned operations through the end of 2027.

Conference Call and Webcast

Codexis will hold a conference call and webcast today beginning at 4:30 pm ET. A live webcast and slide presentation to accompany the conference call will be available on the Investors section of the Company website at www.codexis.com/investors. The conference call dial-in numbers are 877-705-2976 for domestic callers and 201-689-8798 for international callers.

A telephone recording of the call will be available for 48 hours beginning approximately two hours after the completion of the call by dialing 877-660-6853 for domestic callers or 201-612-7415 for international callers. Please use the passcode 13726635 to access the recording. A webcast replay will be available on the Investors section of the Company website for at least 90 days, beginning approximately two hours after the completion of the call.

About Codexis

Codexis is a leading provider of enzymatic solutions for efficient and scalable therapeutics manufacturing, leveraging its proprietary CodeEvolver® technology platform to discover, develop and enhance novel, high-performance enzymes. Codexis enzymes solve for real-world challenges associated with small molecule pharmaceuticals manufacturing and nucleic acid synthesis. The Company is currently developing its proprietary ECO Synthesis® manufacturing platform to enable the scaled manufacture of RNAi therapeutics through an enzymatic route. Codexis’ unique enzymes can drive improvements such as higher yields, reduced energy usage and waste generation, improved efficiency in manufacturing and greater sensitivity in genomic and diagnostic applications. For more information, visit https://www.codexis.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. In some cases, you can identify forward-looking statements by terminology such as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “design,” “due,” “estimate,” “expect,” “goal,” “intend,” “may,” “objective,” “plan,” “positioned,” “potential,” “predict,” “seek,” “should,” “suggest,” “target,” “on track,” “will,” “would” and other similar expressions that are predictions of or indicate future events and future trends, or the negative of these terms or other comparable terminology. To the extent that statements contained in this press release are not descriptions of historical facts, they are forward-looking statements reflecting the current beliefs and expectations of management. These forward-looking statements include, but are not limited to, statements regarding anticipated milestones, including product launches, technical milestones, data releases and public announcements related thereto; Codexis' ability to extend its cash runway through 2027; the market potential of Codexis' ECO Synthesis and ligase businesses; Codexis' 2026 revenue guidance; the timing and completion of the retrofit construction of Codexis' GMP facility; Codexis' ability to advance partnerships with drug innovators toward clinical stage manufacturing agreements; Codexis' ability to expand relationships with CDMO partners and commence strategic partnerships; Codexis' ability to sign a licensing deal with a major pharmaceutical company; Codexis' plans to support commercial launch of pharma biocatalysis products; and Codexis' plan to make presentations at the 2026 TIDES USA Annual Meeting. You should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties and other factors that are, in some cases, beyond Codexis’ control and that could materially affect actual results. Factors that could materially affect actual results include, among others: Codexis' dependence on its licensees and collaborators and the risk that collaborators may terminate their development programs under their respective license agreements with Codexis; Codexis' dependence on a limited number of products and customers, and potential adverse effects to Codexis' business if its customers' products are not received well in the markets; Codexis' ability to successfully develop and commercialize new technology and products for its target markets, including its ECO Synthesis® manufacturing platform and dsRNA ligase; the risk that competitors and potential competitors who have greater resources and experience than Codexis may develop products and technologies that make Codexis' products and technologies obsolete; Codexis' ability to advance partnerships with drug innovators toward clinical stage manufacturing agreements and to establish strategic partnerships with CDMOs; the timing, cost and successful completion of the retrofit construction of Codexis' GMP facility and the risk that the facility may not achieve operational readiness on the anticipated timeline; the risk that the FDA or other regulatory authorities may not accept enzymatically synthesized oligonucleotides or that the regulatory pathway for ECO Synthesis-derived products may be longer or more uncertain than anticipated; Codexis' potential need for additional capital in the future in order to expand its business; Codexis' ability to comply with debt covenants under its loan facility; Codexis' ability to accurately forecast financial and operational performance; the impact of market, political and economic conditions on Codexis' business, financial condition and share price; and the impact of international trade policies, including tariffs, sanctions and trade barriers, on Codexis' business. Additional information about factors that could materially affect actual results can be found in Codexis’ Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC) on March 11, 2026, including under the caption “Risk Factors,” and in Codexis’ other periodic reports filed with the SEC.  Codexis expressly disclaims any intent or obligation to update these forward-looking statements, except as required by law. Codexis’ results for the year and quarter ended December 31, 2025, are not necessarily indicative of our operating results for any future periods.

For More Information
Investor Contact
Georgia Erbez
(650) 421-8100
ir@codexis.com

    
Codexis, Inc.
Condensed Consolidated Statements of Operations
(Unaudited)
(In Thousands, Except Per Share Amounts)

    
 Three Months Ended December 31, Year Ended December 31,
 2025
 2024
 2025
 2024
Revenues:       
Product revenue$5,782  $9,818  $26,028  $36,786 
Research and development revenue 33,133   11,642   44,359   22,559 
Total revenues 38,915   21,460   70,387   59,345 
Costs and operating expenses:       
Cost of product revenue 2,043   3,654   9,338   16,288 
Research and development 11,722   12,099   52,307   46,263 
Selling, general and administrative 11,185   13,049   47,074   55,148 
Restructuring charges 3,407      3,407    
Asset impairment and other charges          165 
Total costs and operating expenses 28,357   28,802   112,126   117,864 
Income (loss) from operations 10,558   (7,342)  (41,739)  (58,519)
Interest income 656   940   2,625   3,670 
Interest and other expense, net (1,595)  (3,970)  (4,813)  (10,393)
Income (loss) before income taxes 9,619   (10,372)  (43,927)  (65,242)
Provision for income taxes 18   4   47   34 
Net income (loss)$9,601  $(10,376) $(43,974) $(65,276)
        
Net income (loss) per share, basic and diluted$0.11  $(0.13) $(0.50) $(0.89)
Weighted average common stock shares used in computing net income (loss) per share, basic 90,396   81,300   87,142   73,408 
Weighted average common stock shares used in computing net income (loss) per share, diluted 90,906   81,300   87,142   73,408 
        


Codexis, Inc.
Condensed Consolidated Statements of Comprehensive Income (Loss)
(Unaudited)
(In Thousands)

    
 Three Months Ended December 31, Year Ended December 31,
 2025
 2024
 2025
 2024
Net income (loss)$9,601  $(10,376) $(43,974) $(65,276)
Other comprehensive income (loss):       
Unrealized gain (loss) on available-for-sale short-term investments, net of tax (5)  (74)  (44)  52 
Comprehensive income (loss)$9,596  $(10,450) $(44,018) $(65,224)
        


Codexis, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(In Thousands)
      
     December 31,
     2025
 2024
Assets   
Current assets:   
 Cash and cash equivalents$50,793  $19,264 
 Restricted cash, current 478   503 
 Short-term investments 27,416   54,194 
 Financial assets:   
  Accounts receivable 8,757   11,920 
  Contract assets 492   4,375 
  Unbilled receivables 1,480   2,751 
   Total financial assets 10,729   19,046 
    Less: allowances (43)  (162)
   Total financial assets, net 10,686   18,884 
 Inventories 1,817   1,799 
 Prepaid expenses and other current assets 5,626   4,128 
   Total current assets 96,816   98,772 
Restricted cash 1,612   1,062 
Investment in non-marketable equity securities 2,498   2,798 
Right-of-use assets - Operating leases, net 30,501   28,700 
Property and equipment, net 13,024   14,197 
Goodwill 2,463   2,463 
Other non-current assets 883   1,019 
   Total assets$147,797  $149,011 
        
Liabilities and Stockholders' Equity   
Current liabilities:   
 Accounts payable 1,554   2,838 
 Accrued compensation 11,042   11,410 
 Other accrued liabilities 2,768   6,223 
 Current portion of lease obligations - Operating leases 2,944   2,827 
 Deferred revenue 7,009   350 
   Total current liabilities 25,317   23,648 
Deferred revenue, net of current portion 360   100 
Long-term lease obligations - Operating leases 30,159   28,163 
Long-term debt 40,105   28,905 
Other long-term liabilities 1,327   1,268 
   Total liabilities 97,268   82,084 
        
Stockholders' equity:   
 Common stock 9   8 
 Additional paid-in capital 657,292   629,673 
 Accumulated other comprehensive income 8   52 
 Accumulated deficit (606,780)  (562,806)
   Total stockholders' equity 50,529   66,927 
   Total liabilities and stockholders' equity$147,797  $149,011 
           

FAQ

What were Codexis (CDXS) revenue results for Q4 2025 and fiscal 2025?

Codexis reported $38.9M in Q4 2025 revenue and $70.4M for fiscal 2025. According to the company, Q4 revenue rose 81% year-over-year largely due to a Merck Technology Transfer Agreement executed in Q4 2025.

How much cash did Codexis (CDXS) have at year-end 2025 and what is the runway?

Codexis held $78.2M in cash, cash equivalents and short-term investments as of December 31, 2025. According to the company, this liquidity is expected to fund planned operations through the end of 2027.

What drove the 2025 gross margin improvement at Codexis (CDXS)?

Product gross margin rose to 64% in fiscal 2025 from 56% in 2024. According to the company, the improvement reflected a sales mix shift toward more profitable products and declines in less profitable legacy products.

What guidance did Codexis (CDXS) provide for 2026 revenue on March 11, 2026?

Codexis issued 2026 revenue guidance of $72M–$76M. According to the company, this guidance reflects expected continued commercial activity and the impact of recent partnerships and agreements.

What strategic partnerships and milestones did Codexis (CDXS) announce for 2026–2027?

Codexis plans to expand CDMO relationships, seek a major pharma licensing deal in H2 2026, and retrofit a GMP facility for full production by end of 2027. According to the company, these steps support commercial scale-up of ECO Synthesis.
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