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DYDYAI

Dyadic (DYAI) Q2 FY26 earnings call: the analyst Q&A

Earnings call· Jun 2026 (Q2 FY26)· Health Care· Aug 12, 2026

Source: earnings call transcript

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

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———

Product announcements

ProductTypeDetails
Proprietary industrial cellulaselaunch

Deals & partnerships

IBT Bioservices OEM distribution agreement

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

Proliant Commercialization 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.

Enzymes Commercialization 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 Bio Commercialization of recombinant DNase 1 and recombinant human and bovine transferrin

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

BRIG Bio Development 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 Foundation Grant program for lower-cost monoclonal antibodies approximately $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 development up to approximately $2.4 million

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

Scripps Research Collaboration for Bundibugyo ebolavirus antigens

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

NIAID Supported preclinical evaluation of C1-produced malaria antigens

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

Israel Institute for Biological Research Monoclonal antibody development

Continuing monoclonal antibody development.

European Vaccines Hub and FBS ecosystem Pursuing additional potential antibody programs

Pursuing additional potential antibody programs.

Undisclosed partner Expanded precision fermented dairy protein portfolio

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

Risks & headwinds

Going concern doubt Next 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 ramp Initial 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 revenue Q2 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

Product revenue ramp

Next quarter
Current Lumpy, initial pilot sales and channel filling
Target Evidence 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.

Find out whether DYAI delivers this. Inve re-checks your case every morning.

Q&A highlights

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 read 6 chapters

Detailed narrative

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.

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.

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.

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.

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.

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.

Summary of the company's earnings call; see how call summaries are prepared. Not investment advice.