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Dyadic Develops Stable C1 Cell Lines and Produces Purified Scripps-Designed Bundibugyo Ebola Antigens from Plasmids in Approximately 15 Days

(Positive)
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Dyadic (Nasdaq: DYAI) reported that, in approximately 15 days after receiving plasmids, it developed stable pools of C1 cell lines and manufactured and initially purified two Scripps-designed Bundibugyo ebolavirus recombinant protein antigens. The C1-produced antigens have been delivered to Fondazione Biotecnopolo di Siena and Scripps Research for preclinical evaluation in support of a potential non-mRNA Bundibugyo ebolavirus vaccine candidate.

According to Dyadic, this rapid turnaround highlights the C1 platform’s potential to accelerate development of vaccines, monoclonal antibodies and other biologics. The company notes C1’s scalability, high antibody titers exceeding 12 g/L in seven days, and the completed receipt of a $3.1 million Gates Foundation grant supporting monoclonal antibody programs.

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Positive

  • 15-day timeline from plasmid receipt to stable C1 pools and purified antigens
  • Delivery of two C1-produced Bundibugyo ebolavirus antigens for preclinical evaluation
  • C1 platform reported antibody titers exceeding 12 g/L in seven days
  • Externally funded collaborations with FBS, CEPI, Gates Foundation and European Vaccines Hub
  • Full receipt of a $3.1 million Gates Foundation grant for monoclonal antibody programs

Negative

  • None.

Market Context

Recent insider records show Net Selling, with 95,392 shares sold and none bought. That context place...
Analysis

Recent insider records show Net Selling, with 95,392 shares sold and none bought. That context places the C1 production update alongside an ownership signal; key watchpoints are repeatable delivery, partner evaluation, and commercialization progress.

Key Figures

Antigen production timeline: approximately 15 days Antigens produced: two antigens Antibody titer: exceeding 12 g/L +2 more
5 metrics
Antigen production timeline approximately 15 days From plasmid receipt to stable pools and initially purified antigens
Antigens produced two antigens Scripps-designed Bundibugyo ebolavirus recombinant protein antigens
Antibody titer exceeding 12 g/L C1-produced monoclonal antibodies
Titer timeline seven days Demonstrated antibody titers exceeding 12 g/L
Gates Foundation grant $3.1 million Support for RSV and malaria monoclonal antibody programs; received in full

Historical Context

5 past events · Latest: Jul 24 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 24 Listing compliance Positive -1.6% Nasdaq confirmed regained compliance and continued listing on the Capital Market
Jul 16 Pipeline expansion Positive -2.5% New industrial enzyme program expanded the bio-industrial pipeline and commercialization model
Jul 07 C1 collaboration Positive +9.6% Global collaborations and funded programs validated C1's biologics manufacturing potential
Jun 29 IP expansion Positive +9.9% Japan patent claims strengthened protection for microbial protein expression technology
Jun 15 Platform validation Positive +16.7% Ebola preparedness activities highlighted C1's approximately 15-day production timeline

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive announcements produced mixed outcomes, with 3 aligned reactions and 2 divergences.

Key Terms

recombinant protein antigens, monoclonal antibodies, preclinical evaluation, viral-clearance
4 terms
recombinant protein antigens medical
"manufactured and initially purified two Scripps-designed Bundibugyo ebolavirus recombinant protein antigens"
Proteins made by using genetic engineering to produce specific parts of a pathogen—usually a surface protein—without the whole virus or bacterium. They act like factory-made puzzle pieces that mimic a germ to train the immune system or to detect antibodies in tests; for investors they signal a product that involves specialized biotech manufacturing, quality controls and regulatory review, which affect cost, scale and commercial timelines.
monoclonal antibodies medical
"vaccine and monoclonal antibody development"
Monoclonal antibodies are lab-made proteins designed to bind a single, specific target on cells or viruses, like identical keys cut to fit one lock. They are used as medicines, tests, or targeted delivery tools and can precisely block or mark disease processes. Investors care because they can become high-value drugs with large sales, long patent protection, and binary risks tied to clinical trial results, regulatory approval, manufacturing scale and pricing.
preclinical evaluation medical
"delivered to FBS and Scripps Research for preclinical evaluation"
Studies and tests done in the lab and in animals to learn how a drug or medical product behaves before it is tried in people. It checks basic safety, how the body absorbs and clears the product, likely effective dose ranges, and early signs of benefit—like crash‑testing and test-driving a prototype before mass production. Investors watch preclinical results because they determine whether a candidate can progress to human trials, shaping timelines, costs, and technical risk.
viral-clearance technical
"does not require the mammalian or insect-cell viral-clearance steps"
Viral clearance is the measurable removal or reduction of a virus from a patient’s body to levels below detection by lab tests, often shown by consecutive negative viral tests or sustained drops in viral load. For investors, it matters because viral clearance is a common clinical trial endpoint and regulatory indicator of a treatment’s effectiveness, and results can influence approval chances, market value, and commercial prospects much like a quality check that determines whether a product can be sold widely.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Delivery of the Bundibugyo viral antigens to Fondazione Biotecnopolo di Siena (“FBS”) and Scripps Research demonstrates C1's potential to accelerate vaccine and monoclonal antibody development, expand platform adoption, and create future commercial opportunities

JUPITER, Fla., July 28, 2026 (GLOBE NEWSWIRE) -- Dyadic International, Inc. (Nasdaq: DYAI) (“Dyadic” or the “Company”), d/b/a Dyadic Applied BioSolutions, today announced that, within approximately 15 days of receiving the plasmids, it developed stable pools of C1 cell lines and manufactured and initially purified two Scripps-designed Bundibugyo ebolavirus recombinant protein antigens.

In response to the active Bundibugyo ebolavirus outbreak, both C1-produced antigens have been delivered to FBS and Scripps Research for preclinical evaluation in support of a potential non-mRNA vaccine candidate targeting Bundibugyo ebolavirus.

The speed of this work is particularly important given the severity and rapid progression of the current outbreak. There is currently no specifically approved vaccine or treatment for Ebola disease caused by Bundibugyo virus.

Dyadic believes these conditions highlight the urgent need for protein-production platforms capable of rapidly developing vaccine antigens, monoclonal antibodies and other biologic countermeasures while also supporting the manufacturing capacity, scalability, affordability and geographic accessibility required for effective outbreak response.

“This is not simply about developing a protein quickly. It is about establishing a potentially faster, more productive, scalable and affordable path for developing and manufacturing non-mRNA vaccines, monoclonal antibodies and other biologics in the quantities needed to respond to active outbreaks and other rapidly evolving health emergencies. When infections can spread faster than conventional countermeasures can be developed and produced, every week matters.” said Mark Emalfarb, Chief Executive Officer of Dyadic.

Emalfarb continued, “Scale flexibility with C1 works in both directions. Production may be expanded to larger microbial bioreactors when substantial quantities or doses are required — or higher yields, greater productivity and shorter bioreactor cycle times may allow manufacturers to produce more protein using a smaller biomanufacturing footprint. That can mean more batches, more protein and more doses from the same manufacturing infrastructure — or potentially less of it. Because C1 is a fungal production system, it also does not require the mammalian or insect-cell viral-clearance steps typically associated with CHO and insect-cell manufacturing, potentially eliminating additional purification operations that can add time, complexity and cost.”

This achievement further validates Dyadic's proprietary C1 platform as a rapid protein production technology that has the potential to support future licensing agreements, commercial manufacturing partnerships, and additional product development opportunities across multiple biologics markets.

In addition to the Bundibugyo ebolavirus antigen program, externally funded and supported collaborations involving FBS, the Coalition for Epidemic Preparedness Innovations (“CEPI”), the Gates Foundation, the European Vaccines Hub and other leading global scientific organizations are helping to advance and validate Dyadic’s rapid C1 protein-development and manufacturing capabilities. C1 has been applied to both vaccine antigens and monoclonal antibodies, with demonstrated antibody titers exceeding 12 g/L in seven days. This includes monoclonal antibody programs targeting respiratory syncytial virus and malaria supported by a $3.1 million grant from the Gates Foundation, which Dyadic has now received in full.

The global biologics sector continues to expand, with industry estimates generally forecasting annual growth in the high-single-digit range and even stronger growth for monoclonal antibodies. This growth is creating a significant potential opportunity for platforms that can accelerate development, increase productivity, scale efficiently and lower manufacturing costs. If C1 can deliver these benefits and gain broader adoption, it could help reshape biologics manufacturing, improve the commercial viability of vaccines, monoclonal antibodies and other therapeutic proteins, and expand patient access in markets where cost, capacity and speed can determine whether treatments are broadly available.

About Dyadic Applied BioSolutions

Dyadic Applied BioSolutions is a global biotechnology company that aims to develop and commercialize scalable, non-animal protein production platforms to meet growing global demand across the life sciences, food and nutrition, and bio-industrial markets. These high-value proteins are designed to enable customers to develop more efficient, scalable, and sustainable products. Dyadic’s proprietary Dapibus™ and C1 expression systems support rapid, cost-effective, and flexible manufacturing.

For more information, please visit http://www.dyadic.com.

Safe Harbor Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act and Section 21E of the Exchange Act, including those regarding Dyadic International’s expectations, intentions, strategies, and beliefs pertaining to future events or future financial performance, such as the success of our clinical trial and interest in our protein production platforms, our research projects and third-party collaborations, as well as the availability of necessary funding. Forward-looking statements generally can be identified by use of the words “expect,” “should,” “intend,” “anticipate,” “will,” “project,” “may,” “might,” “potential,” or “continue” and other similar terms or variations of them or similar terminology. Dyadic International, Inc., and its subsidiaries caution readers that any forward-looking information is not a guarantee of future performance and that actual results could differ materially from those contained in the forward-looking information. Such statements reflect the current views of our management with respect to our operations, results of operations and future financial performance. Forward-looking statements involve many risks, uncertainties, or other factors beyond Dyadic’s control. These factors include, but are not limited to (i) our history of net losses; (ii) market and regulatory acceptance of our microbial protein production platforms and other technologies; (iii) failure to commercialize our microbial protein production platforms or our other technologies; (iv) competition, including from alternative technologies; (v) the results of nonclinical studies and clinical trials; (vi) our capital needs; (vii) changes in global economic and financial conditions; (viii) our reliance on information technology; (ix) our dependence on third parties; (x) government regulations and environmental, social and governance issues; (xi) intellectual property risks; (xii) our ability to comply with the listing standards of the Nasdaq Stock Market LLC; and (xii) other factors discussed in Dyadic’s publicly available filings, including information set forth under the caption “Risk Factors” in Dyadic’s annual report on Form 10-K filed with the Securities and Exchange Commission (“SEC”) on March 25, 2026, as amended on April 30, 2026, and quarterly report on Form 10-Q filed with the SEC on May 13, 2026, as such factors may be updated from time to time in Dyadic’s periodic filings with the SEC, which are accessible on the SEC’s website and at www.dyadic.com. The forward-looking statements contained in this press release are made only as of the date hereof, and except as required by law, we undertake no obligation to publicly update any forward-looking statements for any reason after the date of this press release to conform these statements to actual results or to changes in our expectations.

Media contacts:

Dyadic Applied BioSolutions:
Ping Rawson
Chief Financial Officer
Phone: (561) 743-8333
Email: ir@dyadic.com


FAQ

What did Dyadic (DYAI) announce on July 28, 2026 about Bundibugyo Ebola antigens?

Dyadic announced it developed stable C1 cell lines and produced two Bundibugyo ebolavirus antigens in about 15 days. According to Dyadic, these Scripps-designed antigens were delivered to Fondazione Biotecnopolo di Siena and Scripps Research for preclinical evaluation as part of a potential non-mRNA vaccine effort.

How fast did Dyadic’s C1 platform produce Bundibugyo Ebola antigens and why is this speed important for DYAI investors?

Dyadic reports its C1 platform produced stable pools and purified Bundibugyo antigens in roughly 15 days. According to Dyadic, this rapid turnaround may demonstrate C1’s ability to accelerate development of vaccines and biologics, which could support future licensing, partnerships and commercial opportunities if broadly adopted.

How is Dyadic’s C1 platform being used with Scripps Research and FBS for Bundibugyo ebolavirus?

Dyadic used its C1 platform to manufacture two Scripps-designed Bundibugyo ebolavirus recombinant protein antigens and deliver them to FBS and Scripps. According to Dyadic, these antigens are intended for preclinical evaluation supporting a potential non-mRNA vaccine candidate targeting Bundibugyo ebolavirus during the current outbreak.

What role does the Gates Foundation grant play in Dyadic (DYAI) C1 monoclonal antibody programs?

Dyadic states its C1 platform supports monoclonal antibody programs backed by a $3.1 million Gates Foundation grant. According to Dyadic, this fully received grant supports antibodies targeting respiratory syncytial virus and malaria, where C1 has shown antibody titers exceeding 12 g/L in seven days.

How could Dyadic’s C1 protein production platform impact the growing biologics market for DYAI?

Dyadic believes C1 could address needs for speed, productivity and scalability in a biologics market growing at high single digits annually. According to Dyadic, if C1 gains broader adoption, it may help lower manufacturing costs and expand access to vaccines, monoclonal antibodies and other therapeutic proteins.

What manufacturing advantages does Dyadic highlight for the C1 platform compared with mammalian or insect cell systems?

Dyadic highlights C1’s flexibility to scale in microbial bioreactors and potentially higher yields with shorter cycles. According to Dyadic, C1 is fungal and may avoid mammalian or insect-cell viral-clearance steps, potentially reducing purification operations that add time, complexity and cost in biologics manufacturing.