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Codexis Reports First Quarter 2026 Financial Results

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Codexis (NASDAQ: CDXS) reported Q1 2026 revenue of $15.2 million and reiterated full‑year guidance of $72–$76 million. Product gross margin was 71%; net loss narrowed to $8.7 million ($0.10/share). Cash and short‑term investments totaled $65.1 million, which the company says funds operations through end of 2027.

The company highlighted ECO Synthesis® platform progress, three upcoming TIDES presentations on siRNA stereochemistry and ligation, a 50g siRNA supply agreement for pre‑IND studies, ISO 9001 certification, and plans for an ECO GMP Manufacturing Center.

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Positive

  • Revenue increased to $15.2M in Q1 2026 (from $7.5M in Q1 2025)
  • Product gross margin improved to 71% in Q1 2026 (from 55%)
  • Cash, cash equivalents, and short‑term investments of $65.1M (funding through end of 2027 per company)
  • Reiterated full‑year revenue guidance of $72M–$76M
  • ISO 9001 certification and successful pharmaceutical partner audit for in‑house manufacturing

Negative

  • Net loss of $8.7M in Q1 2026 (still a quarterly loss)
  • R&D and SG&A remain sizable at $11.4M and $9.8M respectively, pressuring near‑term cash burn

Key Figures

Q1 2026 revenue: $15.2M Product gross margin: 71% R&D expenses: $11.4M +5 more
8 metrics
Q1 2026 revenue $15.2M First quarter 2026 vs $7.5M in Q1 2025
Product gross margin 71% Q1 2026 vs 55% in Q1 2025
R&D expenses $11.4M Q1 2026 vs $12.9M in Q1 2025
SG&A expenses $9.8M Q1 2026 vs $12.4M in Q1 2025
Net loss $8.7M ($0.10/share) Q1 2026 vs $20.7M ($0.25/share) in Q1 2025
Cash balance $65.1M Cash, cash equivalents, and short-term investments at Mar 31, 2026
2026 revenue guidance $72M–$76M Full-year 2026 revenue range, reiterated
Licensed products 13 products Enzymes supporting 13 licensed branded pharmaceutical products

Market Reality Check

Price: $2.67 Vol: Volume 1,550,969 is sligh...
normal vol
$2.67 Last Close
Volume Volume 1,550,969 is slightly above the 20-day average of 1,405,473, indicating modestly elevated trading interest around the release. normal
Technical Shares at $2.665 are trading above the 200-day MA of $2.07, but sit about 31% below the 52-week high and well above the 52-week low.

Peers on Argus

CDXS is down about 3.27% while the only peer in the momentum scanner (ACIU) is a...
1 Down

CDXS is down about 3.27% while the only peer in the momentum scanner (ACIU) is also down slightly. Other close peers show mixed moves, suggesting today’s reaction is driven more by company-specific earnings details than a broad sector rotation.

Common Catalyst Another close peer, SLN, also reported quarterly financial results today, pointing to an earnings-driven news cycle in RNA/biotech names rather than a unified price move.

Previous Earnings Reports

5 past events · Latest: Mar 11 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 11 Q4/FY 2025 earnings Positive +34.6% Strong Q4 revenue, improved margins, and 2026 guidance drove a sharp gain.
Nov 06 Q3 2025 earnings Negative -16.9% Revenue decline and restructuring actions overshadowed extended cash runway.
Aug 13 Q2 2025 earnings Positive +1.6% Revenue beat and strong ECO Synthesis momentum supported a modest rise.
May 14 Q1 2025 earnings Negative +1.6% Revenue decline and wider loss contrasted with a small positive price move.
Feb 27 FY 2024 earnings Negative -22.6% Flat-to-lower revenue and sizable annual loss led to a sharp selloff.
Pattern Detected

Earnings events have produced mixed but often strong share reactions, with most reports aligning in direction with the perceived tone of the results.

Recent Company History

Recent earnings releases for Codexis show a pattern of meaningful stock reactions around financial updates. Positive reports, such as Q4/FY 2025 with strong revenue and cash metrics, led to a 34.65% gain, while weaker or more mixed updates, like FY 2024 or Q3 2025, saw declines of 22.65% and 16.95%. Earlier in 2025, Q1 and Q2 earnings with growth in ECO Synthesis and improved margins produced modest gains. Today’s Q1 2026 report, with higher revenue, better margins, and reiterated guidance, fits into this sequence of platform-driven financial progress.

Historical Comparison

-0.3% avg move · Past earnings releases moved the stock by an average of about -0.34%. Today’s -3.27% reaction to Q1 ...
earnings
-0.3%
Average Historical Move earnings

Past earnings releases moved the stock by an average of about -0.34%. Today’s -3.27% reaction to Q1 2026 financials is a larger‑than‑usual downside move versus prior earnings days.

Across recent earnings, Codexis has highlighted ECO Synthesis progress, improving product gross margins, and efforts to extend cash runway, with Q1 2026 continuing this trend via higher revenue, stronger margins, and a reiterated 2026 outlook.

Market Pulse Summary

This announcement highlights Q1 2026 revenue of $15.2M, a stronger 71% product gross margin, and a n...
Analysis

This announcement highlights Q1 2026 revenue of $15.2M, a stronger 71% product gross margin, and a narrowed net loss of $8.7M, alongside cash of $65.1M supporting operations through 2027. Management reiterated full‑year revenue guidance of $72M–$76M and outlined ECO Synthesis milestones, including TIDES presentations and plans for an ECO GMP Manufacturing Center. Investors may track revenue mix, margin trends, and the conversion of ECO Synthesis engagements into larger manufacturing or licensing agreements over time.

Key Terms

phosphorothioate stereochemistry, sirna, pre-ind, cdmo
4 terms
phosphorothioate stereochemistry medical
"demonstrating how the ECO Synthesis® Manufacturing Platform enables control over phosphorothioate stereochemistry."
Phosphorothioate stereochemistry describes the three-dimensional arrangement at a modified link in synthetic DNA/RNA drugs where one oxygen is swapped for sulfur, producing mirror-image forms like left- and right-hand versions of a glove. Those mirror-image forms can alter a drug’s stability, activity and side-effect profile and complicate manufacturing and quality control, so they affect development risk, regulatory review, production cost and commercial reliability for investors.
sirna medical
"Agreed to supply 50g of siRNA using the ECO Synthesis manufacturing platform to enable pre-IND studies."
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.
pre-ind regulatory
"Agreed to supply 50g of siRNA using the ECO Synthesis manufacturing platform to enable pre-IND studies."
"Pre-ind" is short for "pre-indication" and refers to the period before a formal announcement or official signal that a significant change or event is about to happen, such as a company preparing to release important news. For investors, it can signal a time of increased activity or uncertainty, as market participants try to interpret hints and anticipate future developments. Recognizing pre-ind conditions helps investors make more informed decisions ahead of major shifts.
cdmo technical
"Expand our relationships with our CDMO partners with a goal of commencing an additional strategic partnership by the end of 2026."
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.

AI-generated analysis. Not financial advice.

Reports revenue of $15.2 million for the first quarter, company reiterates full-year financial guidance

Three presentations at upcoming TIDES USA annual meeting to feature new data for ECO Synthesis manufacturing platform capabilities

REDWOOD CITY, Calif., May 07, 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 first quarter ended March 31, 2026, and provided a business update.

“Next week Codexis will present new data at the TIDES USA annual meeting demonstrating how the ECO Synthesis® Manufacturing Platform enables control over phosphorothioate stereochemistry. Defined stereochemistry confers overall improved product quality and has the potential to deliver increased potency, a step beyond conventional manufacturing technologies,” said Alison Moore, PhD, President and Chief Executive Officer of Codexis. “We finished the first quarter in a strong financial position with $65.1 million in cash, which we believe remains on track to fund anticipated operations through the end of 2027.”

First Quarter and Recent Business Highlights

  • Received ISO 9001 certification of our in-house manufacturing suite and successfully completed a pharmaceutical partner audit in support of future commercial products.
  • Supported the production of a pharma biocatalysis product which, following successful Phase 3 data, received FDA approval, resulting in a total portfolio of enzymes supporting 13 licensed branded pharmaceutical products.
  • Agreed to supply 50g of siRNA using the ECO Synthesis manufacturing platform to enable pre-IND studies.
  • Achieved successful development milestones of significant ECO Synthesis manufacturing platform capability, enabling siRNA of superior quality.

Upcoming Milestones

  • Codexis will host three presentations at the 2026 TIDES USA annual meeting, taking place from May 11-14, 2026, in Boston. Presentations will (1) showcase enzyme-driven stereoisomer control of siRNA, (2) demonstrate the superior performance of Codexis ligase in siRNA ligation reactions, and (3) discuss the metrics of improved sustainability of the ECO Synthesis manufacturing platform compared to Solid Phase Organic Synthesis.
  • The Company expects to apply for a building permit during the second quarter for its ECO GMP Manufacturing Center in preparation to commence retrofit construction during the second half of 2026. Full production capability is planned by the end of 2027. 
  • Expand our relationships with our CDMO partners with a goal of commencing an additional strategic partnership by the end of 2026.
  • Advance our partnerships with drug innovators toward clinical stage manufacturing agreements.
  • Seeking to sign a licensing deal with a major pharmaceutical company in the second half of 2026.
  • Continue our engagement with the FDA Emerging Technologies team to discuss ECO Synthesis-derived siRNA product quality, stereoisomer control, and product comparability.

First Quarter 2026 Financial Highlights

  • Total revenues were $15.2 million for the first quarter of 2026 compared to $7.5 million in the first quarter of 2025. The increase was primarily due to the recognition of an additional $6.3 million in revenue from the Merck Technology Transfer agreement which we executed during the fourth quarter of 2025.
  • Product gross margin was 71% for the first quarter of 2026 compared to 55% in the first quarter of 2025. 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 and Development expenses for the first quarter of 2026 were $11.4 million compared to $12.9 million in the first quarter of 2025. The decrease was primarily due to lower allocable costs, partially offset by higher employee-related costs and higher use of outside services.
  • Selling, General & Administrative expenses for the first quarter of 2026 were $9.8 million compared to $12.4 million in the first quarter of 2025. The decrease was primarily due to lower employee-related costs due to lower headcount, lower stock-based compensation expenses, and lower consultant fees and outside services.
  • The net loss for the first quarter of 2026 was $8.7 million, or $0.10 per share, compared to a net loss of $20.7 million, or $0.25 per share, for the first quarter of 2025.
  • As of March 31, 2026, Codexis had $65.1 million in cash, cash equivalents, and short-term investments.

2026 Financial Guidance Reiterated

Codexis reiterated its full-year 2026 financial guidance as follows:

  • Total revenues are expected to be in the range of $72 million to $76 million.
  • Codexis expects that its existing cash, cash equivalents, and short-term investments will be sufficient to fund its 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 will be available on the Investors section of the Company website at ir.codexis.com 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, 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 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; 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’ continued engagement with the FDA; 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 presented in this press release are not necessarily indicative of Codexis’ 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 March 31,
  2026   2025 
Revenues:   
Product revenue$7,191  $6,059 
Research and development revenue 8,057   1,484 
Total revenues 15,248   7,543 
Costs and operating expenses:   
Cost of product revenue 2,064   2,732 
Research and development 11,448   12,942 
Selling, general and administrative 9,779   12,355 
Total costs and operating expenses 23,291   28,029 
Loss from operations (8,043)  (20,486)
Interest income 665   751 
Interest and other expense, net (1,290)  (942)
Loss before income taxes (8,668)  (20,677)
Provision for income taxes (36)  (11)
Net loss$(8,704) $(20,688)
    
Net loss per share, basic and diluted$(0.10) $(0.25)
Weighted average common stock shares used in computing net loss per share, basic and diluted 90,768   82,410 
        


Codexis, Inc.
Condensed Consolidated Statements of Comprehensive Loss
(Unaudited)
(In Thousands)
 
 Three Months Ended March 31,
  2026   2025 
Net loss$(8,704) $(20,688)
Other comprehensive loss:   
Unrealized loss on available-for-sale short-term investments, net of tax (19)  (38)
Comprehensive loss$(8,723) $(20,726)
    



Codexis, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(In Thousands)
 
 March 31, 2026 December 31, 2025
Assets   
Current assets:   
Cash and cash equivalents$36,571  $50,793 
Restricted cash, current 425   478 
Short-term investments 28,569   27,416 
Financial assets:   
Accounts receivable 6,777   8,757 
Contract assets 441   492 
Unbilled receivables 852   1,480 
Total financial assets 8,070   10,729 
Less: allowances (43)  (43)
Total financial assets, net 8,027   10,686 
Inventories 2,000   1,817 
Prepaid expenses and other current assets 4,057   5,626 
Total current assets 79,649   96,816 
Restricted cash 1,612   1,612 
Investment in non-marketable equity securities 2,498   2,498 
Right-of-use assets - Operating leases, net 29,566   30,501 
Property and equipment, net 12,588   13,024 
Goodwill 2,463   2,463 
Other non-current assets 994   883 
Total assets$129,370  $147,797 
Liabilities and Stockholders' Equity   
Current liabilities:   
Accounts payable$2,127  $1,554 
Accrued compensation 5,359   11,042 
Other accrued liabilities 3,196   2,768 
Current portion of lease obligations - Operating leases 3,302   2,944 
Deferred revenue 866   7,009 
Total current liabilities 14,850   25,317 
Deferred revenue, net of current portion 350   360 
Long-term lease obligations - Operating leases 29,118   30,159 
Long-term debt 40,483   40,105 
Other long-term liabilities 1,335   1,327 
Total liabilities 86,136   97,268 
    
Stockholders' equity:   
Common stock 9   9 
Additional paid-in capital 658,720   657,292 
Accumulated other comprehensive income (11)  8 
Accumulated deficit (615,484)  (606,780)
Total stockholders' equity 43,234   50,529 
Total liabilities and stockholders' equity$129,370  $147,797 
    



FAQ

What were Codexis (CDXS) Q1 2026 revenues and how do they compare to Q1 2025?

Codexis reported $15.2 million in revenue for Q1 2026, up from $7.5 million in Q1 2025. According to the company, the increase mainly reflects $6.3 million recognized from the Merck technology transfer agreement executed in Q4 2025.

How did Codexis (CDXS) profitability metrics change in Q1 2026?

Product gross margin rose to 71% in Q1 2026 versus 55% a year earlier. According to the company, margin improvement was driven by a shift toward more profitable products and declines in legacy product sales.

What guidance did Codexis (CDXS) provide for full‑year 2026 revenue?

Codexis reiterated full‑year 2026 revenue guidance of $72 million to $76 million. According to the company, this guidance remains unchanged alongside current operational plans and cash forecasts.

How long does Codexis expect its cash to fund operations, per the May 7, 2026 release?

The company states its existing cash, cash equivalents, and short‑term investments of $65.1 million are expected to fund planned operations through the end of 2027. According to the company, this estimate underlies capital and operational planning.

What are Codexis (CDXS) near‑term plans for manufacturing capacity expansion?

The company expects to apply for a building permit in Q2 2026 and begin retrofit construction H2 2026 for an ECO GMP Manufacturing Center, targeting full production capability by the end of 2027. According to the company, this is part of scaling ECO Synthesis.