CI
CODEXIS, INC. (CDXS)·Q4 2024 Earnings Summary
Executive Summary
- Q4 2024 total revenue was $21.5M, up 17% year over year excluding PAXLOVID-related enzyme sales; mix shifted to higher R&D revenue given Pfizer applied the remaining retainer toward a new longer-term agreement, while product revenue was flat versus Q4 2023 excluding PAXLOVID .
- Net loss was $10.4M ($0.13 per share) versus $7.2M ($0.10) in Q4 2023, with product gross margin at 63% (down from 71% ex-PAXLOVID in Q4 2023) due primarily to product mix .
- 2025 guidance introduced: total revenue $64–$68M; Q1 2025 revenue expected $8–$10M with a back-half ramp as ligase/ECO contracts signed in H1 begin execution in H2; company reiterates path to cash-flow positive by end of 2026 and sufficient liquidity to fund operations to that point .
- Strategic catalysts: expected first development contract in H1 2025, pilot-scale GLP-grade siRNA material in 2025, and a GMP scale-up partner by YE 2025; ongoing technical validation via TIDES meetings and expanding feasibility work with major siRNA innovators and CDMOs .
- Management tone confident: “commercial lift-off” for ECO Synthesis in 2025, prioritizing multi-asset partners, and balancing disclosure with partner confidentiality to protect competitive advantage .
What Went Well and What Went Wrong
What Went Well
- R&D revenue increased to $11.6M (vs. $8.5M in Q4 2023) on recognition of the remaining Pfizer retainer tied to a new longer-term agreement, creating future revenue opportunities; total revenue rose 17% YoY excluding PAXLOVID .
- ECO Synthesis platform advanced materially: first-ever end-to-end enzymatic synthesis of an approved siRNA (inclisiran) and four synthesis routes demonstrated; increased partner interest and successful feasibility studies, positioning for revenue-generating contracts in 2025 .
- Liquidity and outlook: $73.5M in cash, cash equivalents and short-term investments at YE 2024; 2025 revenue guidance $64–$68M and reiterated path to cash-flow positive by end of 2026 .
Management quotes
- “We are ready to convert ongoing collaborations into formal revenue-generating contracts” – Stephen Dilly, CEO .
- “2025 is slated to be the year we achieve commercial lift off for the ECO Synthesis platform” – Stephen Dilly, CEO .
- “We continue to expand our ligation services… competing and winning… with 4 new companies engaged at different stages” – Kevin Norrett, COO .
What Went Wrong
- Product gross margin compressed to 63% (Q4 2024) from 71% in Q4 2023 ex-PAXLOVID, driven largely by product mix; management plans to retire/divest lower-margin products to improve margins in 2025 .
- Net loss widened versus prior year ($10.4M vs. $7.2M in Q4 2023), with SG&A up (to $13.0M) due to costs associated with executive departures and R&D expenses up to $12.1M from lab supplies and manufacturing services .
- Ongoing revenue concentration/lumpiness: Q1 historically weakest, with explicit Q1 2025 guidance of $8–$10M and a back-half ramp dependent on execution of new ligase/ECO contracts and GMP scale-up partner timing .
Financial Results
Quarterly Trend (sequential comparison)
Year-over-Year Comparison (Q4 2023 vs. Q4 2024)
Segment Breakdown (Revenue)
KPIs and Balance Sheet Highlights
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- Strategic focus: “We are ready to convert ongoing collaborations into formal revenue-generating contracts” (CEO) .
- 2025 inflection: “2025 is slated to be the year we achieve commercial lift off for the ECO Synthesis platform” (CEO) .
- Commercial execution: “We continue to expand our ligation services… competing and winning… with 4 new companies engaged” (COO) .
- Margin and mix: “Gross margins have been a focus… retiring or divesting lower-margin products… expect ongoing improvement” (CFO) .
- Liquidity outlook: “Ended 2024 with $73.5M… sufficient to fund planned operations through achieving cash flow positive by end of 2026” (CFO) .
Q&A Highlights
- Partner confidentiality and disclosure: Management will disclose progress (capacity filled, number of partners) but not names/assets due to competitive sensitivities; joint scientific presentations used for validation .
- Pipeline of engagements: ~7 customers engaged across ligation and ECO synthesis; multifaceted agreements expected; toolbox approach rather than cookie-cutter .
- Gross margin trajectory: Aim to improve in 2025 via product mix optimization and retiring lower-margin SKUs; 2023 margins “artificially inflated” by one-offs .
- GMP scale-up partner: Multiple candidates in late-stage discussions; partnership expected to minimize Codexis’ near-term spend and accelerate GMP pathway, buying time to build own facility .
- Small innovator model: Will consider economic rights (milestones/royalties) with modest upfronts in exchange for comprehensive CMC/analytical support .
- Pfizer relationship: Recognition of remaining PAXLOVID retainer tied to new longer-term agreement for non-COVID programs, creating future revenue opportunities .
Estimates Context
- We attempted to retrieve Q4 2024 and FY 2025 S&P Global consensus estimates for revenue and EPS, but the request was unsuccessful due to a data provider daily limit; therefore, comparisons to Wall Street consensus are not available in this report [GetEstimates error].
- Management indicated FY 2024 revenues would fall within the current range of analyst estimates during the Q3 call, but did not specify values; we do not impute or estimate consensus .
Key Takeaways for Investors
- Sequential momentum and mix shift: Q4 revenue accelerated to $21.5M with R&D revenue strength tied to Pfizer; 2025 revenue guide ($64–$68M) and Q1 guide ($8–$10M) suggest H2 weighting as ligase/ECO contracts convert into execution – monitor H1 contract signings and H2 delivery .
- Margin work-in-progress: Product gross margin at 63% (vs. 71% ex-PAXLOVID YoY) reflects mix; management targets margin improvement via SKU optimization – watch product mix and incremental ligase orders for margin uplift .
- ECO/ligase commercialization: Technical leadership validated (inclisiran end-to-end enzymatic synthesis, Bachem poster); “commercial lift-off” in 2025 with first development contracts, GLP-grade production, and a GMP scale-up partner by YE 2025 – key catalysts for stock narrative .
- Liquidity runway and profitability: $73.5M cash/investments at YE; company expects to be cash-flow positive by end of 2026 without relying on own GMP facility near term – reduces financing risk .
- Partner breadth and confidentiality: Expect announcements focused on capacity and project wins rather than named partners; investor updates may be through scientific meetings and joint posters – set expectations accordingly .
- Strategic portfolio actions: Non-core asset licensing (e.g., Alphazyme royalties) and ATM raise extended runway; continued focus on pharma biocatalysis growth and siRNA manufacturing capabilities .
- Trading implications: Near-term stock moves likely tied to H1 contract announcements and YE 2025 GMP partner disclosure; medium-term thesis hinges on ECO/ligase adoption, margin improvement, and delivery against the 2025 revenue guide .