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    DYAI
    Earnings call· Jun 2026(Q2 FY26)

    DYADIC INTERNATIONAL Q2 FY26 earnings call DYAI

    Aug 12, 2026 Source

    Executive summary

    Dyadic Q2 FY26 — Commercial Transition Gains Traction Amidst Going Concern Disclosure

    Dyadic is actively transitioning from a technology platform developer to a commercially driven business, evidenced by initial product sales and partner-led commercialization across life sciences, food and nutrition, and bioindustrial markets. The company is also advancing its biopharmaceutical programs through external funding, validating its C1 platform's capabilities in speed and productivity. Despite these operational advancements, the company faces significant liquidity challenges, leading to a going concern disclosure, and is actively pursuing various financing alternatives, including non-dilutive capital and strategic partnerships, to strengthen its balance sheet and fund future growth.

    Highlights

    5
    • Productivity in the animal-free recombinant human transferrin program increased by approximately 80%, expected to reduce costs by approximately 40%.

    • Total revenue for the first six months of 2026 increased approximately 52% to $2.1 million compared to $1.4 million in 2025.

    • The C1 platform demonstrated the ability to progress from plasmid to purified protein antigen in approximately 15 days.

    • Initial pilot sales were generated for recombinant transferrin and growth factors for cultivated meat applications.

    • Partner-developed products, such as Enzymes' non-animal bovine chymosin and Fermbox Bio's recombinant DNase 1 and transferrin, are generating commercial sales.

    Concerns

    5
    • Substantial doubt exists about the company's ability to continue as a going concern under ASC 205-3 due to its current liquidity position of $4.8 million in cash and equivalents.

    • Total revenue for Q2 FY26 was essentially flat at $961,000 compared to $967,000 in Q2 FY25.

    • Total cost of revenue for Q2 FY26 increased by 60% to $984,000 compared to $614,000 in Q2 FY25.

    • Loss from operations for Q2 FY26 was $2.1 million, compared to $1.7 million in the prior year period.

    • Net loss for Q2 FY26 was $2.1 million or $0.06 per share, compared to $1.8 million or $0.06 per share in Q2 FY25.

    Segment performance

    4
    SegmentRevenueYoYQoQMargin
    Life Sciences
    Focus on improving manufacturing economics and expanding distribution through OEM partners and direct sales for research, diagnostic, and cell culture applications.
    Productivity improvement (recombinant human transferrin): 80%Cost reduction (recombinant human transferrin): 40%Product shipments to IBT Bioservices (OEM distribution agreement)Initial pilot sales (recombinant transferrin and growth factors for cultivated meat applications)Proliant commercialization: Albufree Dx (launched), Albufree Tx (planned), Albufree CGT (planned)
    Food and Nutrition
    Commercial validation through partner sales and new development agreements, leveraging the same development work across multiple markets for earlier market validation and revenue.
    Enzymes commercial sales: non-animal bovine chymosin (generating sales)Fermbox Bio commercialization: recombinant DNase 1, recombinant human and bovine transferrin (expanded)BRIG Bio development agreement: recombinant bovine alpha-lactalbumin (scale-up initiated)Precision fermented dairy protein portfolio: expanded through additional development and commercialization agreement
    Bioindustrial
    Building a portfolio around scalable enzyme production, with a new cellulase product for advanced fiber modification applications, leveraging the Dapibus platform.
    New product: proprietary industrial cellulase (announced July)
    Biopharmaceutical Programs
    Partner-funded and capital-efficient strategy, generating data for monoclonal antibodies and vaccine antigens, validating C1's capabilities in productivity, quality, and speed.
    Gates Foundation grant: approximately $3.9 million (focused on lower-cost monoclonal antibodies for RSV and malaria)CEPI-supported collaboration (through FBS): up to approximately $2.4 million (for recombinant vaccine development)Speed to protein: 15 days (plasmid to purified protein antigen)NIAID-supported evaluation: C1-produced malaria antigens (preclinical evaluation)Monoclonal antibody development: with Israel Institute for Biological Research
    $837,000

    Operational metrics

    33
    Total revenue
    $961,000flat compared to Q2 FY25
    Q2 FY26

    Total revenue for the three months ended June 30, 2026 was approximately $961,000, essentially flat compared to approximately $967,000 for the second quarter of 2025.

    Total revenue
    $967,000
    Q2 FY25

    Total revenue for the three months ended June 30, 2026 was approximately $961,000, essentially flat compared to approximately $967,000 for the second quarter of 2025.

    Total revenue
    $2.1 millionup 52% YoY
    6 months FY26

    For the first six months of 2026, total revenue increased approximately 52% to $2.1 million compared to approximately $1.4 million for the same period in 2025.

    Total revenue
    $1.4 million
    6 months FY25

    For the first six months of 2026, total revenue increased approximately 52% to $2.1 million compared to approximately $1.4 million for the same period in 2025.

    Research and development revenue
    $124,000
    Q2 FY26

    Revenue for the quarter included approximately $124,000 of research and development revenue and $837,000 of grant revenue, primarily associated with our ongoing externally funded programs.

    Grant revenue
    $837,000
    Q2 FY26

    Revenue for the quarter included approximately $124,000 of research and development revenue and $837,000 of grant revenue, primarily associated with our ongoing externally funded programs.

    Total cost of revenue
    $984,000up 60% YoY
    Q2 FY26

    Total cost of revenue for the quarter was approximately $984,000, an increase of 60% compared to approximately $614,000 for the second quarter of 2025. The increase was primarily related to higher activity levels associated with our grant-funded programs.

    Total cost of revenue
    $614,000
    Q2 FY25

    Total cost of revenue for the quarter was approximately $984,000, an increase of 60% compared to approximately $614,000 for the second quarter of 2025.

    Internal research and development expenses
    $333,000down 47% YoY
    Q2 FY26

    Internal research and development expenses decreased 47% year over year to approximately $333,000 compared to approximately $629,000 in the second quarter of 2025.

    Internal research and development expenses
    $629,000
    Q2 FY25

    Internal research and development expenses decreased 47% year over year to approximately $333,000 compared to approximately $629,000 in the second quarter of 2025.

    Internal research and development expenses
    $809,000down 28% YoY
    6 months FY26

    For the six months, internal research and development expenses were approximately $809,000, down 28% from approximately $1.1 million a year ago.

    Internal research and development expenses
    $1.1 million
    6 months FY25

    For the six months, internal research and development expenses were approximately $809,000, down 28% from approximately $1.1 million a year ago.

    G&A expenses
    $1.7 millionup 18% YoY
    Q2 FY26

    G&A expenses increased by $253,000 or 18% year over year to approximately $1.7 million compared to approximately $1.4 million in the second quarter of 2025.

    G&A expenses
    $1.4 million
    Q2 FY25

    G&A expenses increased by $253,000 or 18% year over year to approximately $1.7 million compared to approximately $1.4 million in the second quarter of 2025.

    G&A expenses
    $3.4 millionup 14% YoY
    6 months FY26

    For the six months, G&A expenses were approximately $3.4 million and an increase of 14% year over year.

    Rebranding and business development expenses
    $323,000
    Q2 FY26

    The increase was primarily driven by higher rebranding and business development expenses of $323,000 and the higher legal and accounting expenses of $116,000, partially offset by lower share-based compensation expenses of $196,000 and the lower incentive compensation of $32,000.

    Legal and accounting expenses
    $116,000
    Q2 FY26

    The increase was primarily driven by higher rebranding and business development expenses of $323,000 and the higher legal and accounting expenses of $116,000, partially offset by lower share-based compensation expenses of $196,000 and the lower incentive compensation of $32,000.

    Share-based compensation expenses
    lower by $196,000
    Q2 FY26

    partially offset by lower share-based compensation expenses of $196,000 and the lower incentive compensation of $32,000.

    Incentive compensation
    lower by $32,000
    Q2 FY26

    partially offset by lower share-based compensation expenses of $196,000 and the lower incentive compensation of $32,000.

    Loss from operations
    $2.1 millionvs $1.7 million in prior year
    Q2 FY26

    Loss from operations for the quarter was approximately $2.1 million compared to approximately $1.7 million in the prior year period.

    Loss from operations
    $1.7 million
    Q2 FY25

    Loss from operations for the quarter was approximately $2.1 million compared to approximately $1.7 million in the prior year period.

    Net loss
    $2.1 millionvs $1.8 million in Q2 FY25
    Q2 FY26

    Net loss for the quarter was approximately $2.1 million or $0.06 per share, compared to approximately $1.8 million or $0.06 per share for the second quarter of 2025.

    Net loss
    $1.8 million
    Q2 FY25

    Net loss for the quarter was approximately $2.1 million or $0.06 per share, compared to approximately $1.8 million or $0.06 per share for the second quarter of 2025.

    EPS
    $0.06vs $0.06 in Q2 FY25
    Q2 FY26

    Net loss for the quarter was approximately $2.1 million or $0.06 per share, compared to approximately $1.8 million or $0.06 per share for the second quarter of 2025.

    EPS
    $0.06
    Q2 FY25

    Net loss for the quarter was approximately $2.1 million or $0.06 per share, compared to approximately $1.8 million or $0.06 per share for the second quarter of 2025.

    Net loss
    $4.1 millionvs $3.8 million in 6 months FY25
    6 months FY26

    For the six months ended June 30, 2026, net loss was approximately $4.1 million or $0.11 per share compared to approximately $3.8 million or $0.13 per share for the first six months of 2025.

    Net loss
    $3.8 million
    6 months FY25

    For the six months ended June 30, 2026, net loss was approximately $4.1 million or $0.11 per share compared to approximately $3.8 million or $0.13 per share for the first six months of 2025.

    EPS
    $0.11vs $0.13 in 6 months FY25
    6 months FY26

    For the six months ended June 30, 2026, net loss was approximately $4.1 million or $0.11 per share compared to approximately $3.8 million or $0.13 per share for the first six months of 2025.

    EPS
    $0.13
    6 months FY25

    For the six months ended June 30, 2026, net loss was approximately $4.1 million or $0.11 per share compared to approximately $3.8 million or $0.13 per share for the first six months of 2025.

    Cash, cash equivalents, restricted cash and investment-grade securities
    $4.8 million
    Q2 FY26

    we ended the second quarter with approximately $4.8 million in cash, cash equivalents, restricted cash and investment-grade securities including accrued interest.

    Productivity improvement
    80%
    Q2 FY26

    our initial pilot-scale run increased productivity by approximately 80%.

    Cost reduction
    40%
    Q2 FY26

    Based on our current preliminary biomanufacturing assumptions, that improvement is expected to reduce costs by approximately 40%.

    Plasmid-to-purified-protein capability
    15 days
    Q2 FY26

    That work has demonstrated the ability in certain programs to move from plasmid-to-purified-protein in approximately 15 days.

    Industry KPIs

    3
    MetricValueDetails
    Pipeline read out calendarPreclinical studies initiation for C1-produced mAbs (RSV/malaria); further characterization/potential preclinical evaluation for Bundibugyo ebolavirus antigens; ongoing preclinical evaluation for C1-produced malaria antigens.
    Clinical trial efficacy safety dataHigh productivity and functional characteristics comparable to established mammalian cell reference materials
    Collaboration milestone royalty revenuePotential for additional milestone and future royalty economics

    Product announcements

    1
    ProductTypeDetails
    Proprietary industrial cellulaselaunch

    Deals & partnerships

    12
    IBT BioservicesOEM distribution agreement

    OEM distribution agreement for product shipments for research, diagnostic and cell culture applications.

    ProliantCommercialization of Albufree Dx, Albufree Tx, Albufree CGT

    Proliant has begun commercialization of Albufree Dx recombinant human albumin for life science and diagnostic applications and has announced plans to broaden the portfolio with Albufree Tx for cell culture and Albufree CGT for cell and gene therapy applications.

    EnzymesCommercialization of non-animal bovine chymosin

    Their non-animal bovine chymosin produced using Dyadic technology is now generating commercial sales. A second product is also in development.

    Fermbox BioCommercialization of recombinant DNase 1 and recombinant human and bovine transferrin

    Commercialization has expanded around recombinant DNase 1 and recombinant human and bovine transferrin.

    BRIG BioDevelopment agreement for recombinant bovine alpha-lactalbumin

    Initiated scale-up activities with BRIG Bio for recombinant bovine alpha-lactalbumin under a fully funded development agreement.

    Gates FoundationGrant program for lower-cost monoclonal antibodiesapproximately $3.9 million

    Grant program focused on developing potentially lower-cost monoclonal antibodies targeting respiratory syncytial virus and malaria.

    CEPI Foundation (through FBS)Collaboration for recombinant vaccine developmentup to approximately $2.4 million

    Collaboration to support recombinant vaccine development and scale-up activities.

    Scripps ResearchCollaboration for Bundibugyo ebolavirus antigens

    Applied rapid workflow to two Scripps-designed Bundibugyo ebolavirus antigens, delivered for characterization and potential preclinical evaluation.

    NIAIDSupported preclinical evaluation of C1-produced malaria antigens

    Advancing NIAID-supported preclinical evaluation of C1-produced malaria antigens.

    Israel Institute for Biological ResearchMonoclonal antibody development

    Continuing monoclonal antibody development.

    European Vaccines Hub and FBS ecosystemPursuing additional potential antibody programs

    Pursuing additional potential antibody programs.

    Undisclosed partnerExpanded precision fermented dairy protein portfolio

    Expanded precision fermented dairy protein portfolio through an additional development and commercialization agreement.

    Risks & headwinds

    3
    Going concern doubtNext 12 months from financial statement issuance date

    Ended Q2 FY26 with approximately $4.8 million in cash, cash equivalents, restricted cash and investment-grade securities.

    Mitigation: Actively evaluating a range of financing alternatives, including non-dilutive and strategic sources (licensing, upfront/milestone payments, royalties, funded development, partnerships); disciplined cash management; expanding commercial revenues; maximizing third-party funding.

    Lumpy product revenue rampInitial quarters of commercialization

    Initial pilot sales and channel filling, but too early for recurring orders.

    Mitigation: Ongoing discussions, leveraging partners (Proliant, Enzymes, Fermbox), exploring other distribution opportunities.

    Increased cost of revenueQ2 FY26

    Total cost of revenue for Q2 FY26 was approximately $984,000, an increase of 60% compared to approximately $614,000 for Q2 FY25.

    Mitigation: Primarily related to higher activity levels associated with grant-funded programs, implying it's tied to revenue-generating activities.

    What to watch in Q3 FY26

    5

    Product revenue ramp

    Next quarter
    CurrentLumpy, initial pilot sales and channel filling
    TargetEvidence of recurring orders and increasing momentum

    Why it matters

    Demonstrates successful commercial transition and contributes to financial stability.

    Yes, lumpy would probably be the best way to describe it. What we did in the second quarter, we started to fill the channels... But it's too early until we have some recurring orders to really figure out what that ramp is going to look like.

    Q&A highlights

    4

    Will product revenues be seen in Q3, and what will the ramp look like (lumpy vs. steady)?

    Joe Hazelton confirmed that product revenues are expected to be 'lumpy' initially, as the company is filling channels and generating initial pilot sales. He noted it's too early to predict a steady ramp but highlighted ongoing discussions and partner commercialization efforts (Proliant, Enzymes, Fermbox) to build momentum.

    Yes, lumpy would probably be the best way to describe it. What we did in the second quarter, we started to fill the channels. We obviously shipped products to our first global distributor, IBT. We also have direct product sales or initial pilot sales going into cultured meat and a couple into the research segment as well. But it's too early until we have some recurring orders to really figure out what that ramp is going to look like.

    asked by Matt Hewitt · answered by Joseph Hazelton

    2 min read6 chapters

    Detailed Narrative

    01

    Transition to Commercial Business

    Dyadic is shifting from primarily developing technology platforms to building a commercially driven business. This transition involves shipping products, supporting customer evaluations, generating initial sales, and expanding distribution. A key aspect is improving manufacturing economics, as demonstrated by an 80% productivity increase in the animal-free recombinant human transferrin program, which is expected to reduce costs by 40%. This commercial activity is leveraged to create broader opportunities for partnerships and licensing.

    02

    Platform Validation and Scalability

    The company's C1 and Dapibus platforms are being validated across various markets. The significant productivity improvement in transferrin not only enhances product economics but also serves as a data point to prospective partners, demonstrating the platform's ability to manufacture proteins more efficiently and economically. The Dapibus platform is highlighted for its repeatable product development and manufacturing capabilities across multiple enzyme classes and end markets, streamlining strain development, process optimization, and scale-up.

    03

    Biopharmaceutical Program Progress

    Biopharma programs are generating critical data for monoclonal antibodies (mAbs) and vaccine antigens, supported by partners like the Gates Foundation and CEPI. C1-produced antibodies have shown high productivity and functional characteristics comparable to established mammalian cell reference materials. A notable achievement is the C1 platform's ability to progress from plasmid to purified protein antigen in approximately 15 days, a capability crucial for pandemic preparedness and overall development timelines.

    04

    Strategic Partnerships and Revenue Pathways

    Dyadic employs a capital-efficient distribution strategy, combining selective direct sales with distributors and OEM partners. Relationships with IBT Bioservices, Proliant, Enzymes, Fermbox Bio, and BRIG Bio illustrate various stages of commercialization, from distribution to initial sales and partner-led commercial sales. These collaborations are designed to create multiple potential revenue streams for Dyadic, including direct sales, partner sales, milestones, royalties, development funding, and licensing.

    05

    Financial Overview and Liquidity Challenge

    Total revenue for the first six months of 2026 increased 52% to $2.1 million, primarily driven by grant-funded programs. However, Q2 FY26 revenue was flat year-over-year at $961,000, and the company reported a loss from operations of $2.1 million and a net loss of $2.1 million ($0.06 per share). The company ended Q2 with $4.8 million in cash and equivalents, leading to a 'going concern' disclosure due to insufficient capital for the next 12 months, despite being in compliance with all debt covenants.

    06

    Capital Strategy and Future Outlook

    To address liquidity concerns, Dyadic is actively evaluating a range of financing alternatives, including non-dilutive and strategic sources such as new licensing arrangements, upfront and milestone payments, royalties, and funded development programs. The objective is to increasingly fund product development through commercial revenues and partner-funded programs, thereby reducing reliance on dilutive capital and extending financial resources while carefully managing operating expenses and capital requirements.

    AI-generated summary of the company’s earnings call. Not investment advice.