Investor presentation
Logotype for Dyadic International Inc

Dyadic International (DYAI) Investor presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Dyadic International Inc

Investor presentation summary

1 May, 2026

Platform overview and technology

  • Rapid, scalable microbial platform enables animal-free protein production for life sciences, diagnostics, and biomanufacturing.

  • Engineered C1 fungal strain supports high-yield, low-viscosity fermentation and humanized glycosylation.

  • Stable production strains can be generated in as little as three weeks, significantly faster than traditional CHO systems.

  • Industrial-scale fermentation validated at >100,000L, using standard equipment and fed-batch technology.

  • Platform supports a wide range of biologics, including vaccine antigens, monoclonal antibodies, and complex proteins.

Performance, productivity, and cost advantages

  • C1 platform offers cell doubling time of ~2.5 hours and production cycles of 7–9 days, outperforming CHO and insect systems.

  • Achieves up to 10–40x higher yields than baculovirus systems and multi-gram per liter titers in 4–7 days.

  • Lower cost of goods due to rapid fermentation, high productivity, and no need for viral clearance steps.

  • Multiple engineering strategies, including combinatorial libraries and fermentation optimization, have demonstrated 6–8x productivity improvements.

  • Humanized glycosylation patterns achieved with >98% humanized glycans and >92% occupancy.

Safety, regulatory, and clinical validation

  • C1 host is non-pathogenic, FDA GRAS, with no mammalian viral contamination risk and a controlled impurity profile.

  • Platform purification processes are comparable to other biologics, and safety demonstrated in successful Phase I clinical trial.

  • Comparability confirmed between GLP and GMP batches for vaccine candidates, with all parameters within acceptance criteria.

  • Phase I study of DYAI-100 vaccine met primary safety endpoint and induced robust immune responses.

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