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Triera Biosciences Completes Innovative Solutions Canada Contract, Advances Platform Toward New Candidate Development

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Triera Biosciences (ZTEK) completed an Innovative Solutions Canada program and has begun an Ontario Centres of Innovation Collaborate 2 Commercialize agreement to advance its aptamer platform toward seasonal influenza candidates. The OCI C2C project budget is approximately $300,000 with matched cash contributions from OCI and Zentek.

Triera selected an H5N1-binding aptamer in ~7 weeks and will apply multivalent aptamer engineering to H1N1, H3N2 and expanded strains, with workstreams including dose-finding, PK/PD modeling and initiation of GLP-style toxicology and immunogenicity studies.

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AI-generated analysis. Not financial advice.

Positive

  • $300,000 OCI C2C project budget with matched cash contributions
  • Aptamer selection achieved in ~7 weeks, demonstrating rapid platform speed
  • Program expands coverage to H1N1, H3N2 and H7N9, showing multi-subtype applicability

Negative

  • Full technical report pending from project partners, limiting public data availability
  • GLP-style toxicology and immunogenicity studies are only initiating, preclinical program not yet complete

News Market Reaction – ZTEK

-5.74% 3.2x vol
4 alerts
-5.74% News Effect
-9.2% Trough Tracked
-$3M Valuation Impact
$54.87M Market Cap
3.2x Rel. Volume

On the day this news was published, ZTEK declined 5.74%, reflecting a notable negative market reaction. Argus tracked a trough of -9.2% from its starting point during tracking. Our momentum scanner triggered 4 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $3M from the company's valuation, bringing the market cap to $54.87M at that time. Trading volume was very high at 3.2x the daily average, suggesting heavy selling pressure.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

OCI C2C project budget: $300,000 Global infection rate: 20% of global population (~1.66 billion people) Severe infection cases: 3 to 5 million cases +5 more
8 metrics
OCI C2C project budget $300,000 Total approved OCI Collaborate 2 Commercialize budget
Global infection rate 20% of global population (~1.66 billion people) Estimated annual seasonal influenza infections
Severe infection cases 3 to 5 million cases Estimated annual severe seasonal influenza infections
Annual deaths 290,000 to 650,000 deaths Estimated annual deaths from seasonal influenza
HA subtype H1 H1 Hemagglutinin subtype targeted by aptamer platform
HA subtype H3 H3 Hemagglutinin subtype targeted by aptamer platform
Influenza A subtypes H1N1 and H3N2 Most commonly circulating seasonal Influenza A strains
Additional strain H7N9 Additional influenza strain for expanded aptamer strain coverage

Market Reality Check

Price: $0.8667 Vol: Volume 88,961 is 1.56x th...
high vol
$0.8667 Last Close
Volume Volume 88,961 is 1.56x the 20-day average of 57,030, indicating elevated trading interest pre-announcement. high
Technical Shares at $0.54 are trading below the 200-day MA of $0.77 and about 70.67% under the 52-week high of $1.8411.

Peers on Argus

While ZTEK was down 1.24%, several Healthcare/Medical Instruments peers were pos...
1 Up

While ZTEK was down 1.24%, several Healthcare/Medical Instruments peers were positive pre-news (PDEX +1.95%, ZJYL +3.59%, KRMD +3.09%, UTMD +2.52%). Only one peer (NYXH +6.42%) appeared in momentum scans, supporting a stock-specific move rather than a sector-wide reaction.

Historical Context

5 past events · Latest: Apr 09 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Apr 09 Graphite PEA mandate Positive -0.9% Albany Graphite engages Micon to complete new NI 43‑101 PEA.
Apr 01 Market-making deal Positive +3.6% Engagement of ICP Securities for automated market‑making services.
Mar 25 Triera CRO launch Positive -2.8% Launch of Triera CRO services for custom aptamer and biosensor work.
Mar 13 Litigation outcome Positive -1.9% Favorable court judgment dismissing most claims against Zentek.
Mar 09 PDAC 2026 update Positive +0.5% Government and First Nations engagement for Albany Graphite at PDAC.
Pattern Detected

Recent news has often been positive while the stock shows mixed to negative next-day reactions, with more divergences than alignments.

Recent Company History

Over the last two months, Zentek has released a series of operational and strategic updates. These include Albany Graphite’s new PEA mandate on Apr 9, 2026, a market‑making agreement on Apr 1, Triera’s CRO launch on Mar 25, favorable litigation outcomes on Mar 13, and a PDAC engagement update on Mar 9. Despite generally constructive content, three of these five items saw negative next‑day price moves, suggesting that positive announcements have not consistently translated into immediate share price strength. Today’s Triera platform progress fits into this pattern of technical and strategic milestones.

Market Pulse Summary

The stock moved -5.7% in the session following this news. A negative reaction despite positive opera...
Analysis

The stock moved -5.7% in the session following this news. A negative reaction despite positive operational progress fits Zentek’s recent pattern, where constructive news on Triera and Albany Graphite sometimes preceded weak next‑day trading. The company entered this announcement at $0.54, well below its 200‑day MA of $0.77 and 70.67% under its 52‑week high, which already reflected cautious sentiment. In this context, further downside would have raised questions about financing needs, Nasdaq bid‑price compliance, and whether ongoing technical milestones are sufficient to improve market confidence.

Key Terms

aptamer, hemagglutinin, pharmacokinetic/pharmacodynamic, GLP-style toxicology, +4 more
8 terms
aptamer medical
"the development of an aptamer-based asset for binding and deactivating H5N1"
An aptamer is a short strand of DNA, RNA or a small protein engineered to stick tightly and specifically to a particular molecule, like a lock fitting a key. Investors care because aptamers can function like artificial antibodies for diagnostics, drugs, or targeted delivery, offering potential advantages in cost, stability and manufacturing that can affect a product’s development speed, regulatory path and commercial value.
hemagglutinin medical
"engineering principles to hemagglutinin (HA) subtypes H1 and H3"
Hemagglutinin is a protein on the surface of certain viruses that acts like a key, allowing the virus to attach to and enter human cells and sometimes causing red blood cells to clump together. Investors care because changes in hemagglutinin can alter how easily a virus spreads and how well vaccines or antiviral drugs work, making it a central focus for vaccine design, regulatory decisions, and market reactions to clinical or public-health news.
pharmacokinetic/pharmacodynamic medical
"Dose-finding and pharmacokinetic/pharmacodynamic modeling to define the protective"
Pharmacokinetic/pharmacodynamic (PK/PD) describes two linked ideas: pharmacokinetics is how a drug moves through the body (how fast it’s absorbed, spread, broken down and eliminated) and pharmacodynamics is how the drug affects the body (the relationship between dose and response). Investors care because strong, predictable PK/PD data reduce uncertainty about effective dosing, safety and likelihood of regulatory approval—similar to knowing a car’s fuel efficiency and braking before buying, which lowers the risk of a costly surprise.
GLP-style toxicology medical
"Initiation of GLP-style toxicology and immunogenicity studies oriented toward"
GLP-style toxicology describes preclinical safety studies conducted using procedures and documentation similar to formal Good Laboratory Practice (GLP) standards, though they may not be fully GLP-certified. Investors care because these studies aim to reveal potential drug or chemical harms and show whether safety data is collected reliably—think of a dress rehearsal that follows the rules but might lack the official stamp; stronger, GLP-standard data reduces regulatory and development risk.
immunogenicity medical
"GLP-style toxicology and immunogenicity studies oriented toward Health Canada"
Immunogenicity is the ability of a substance, such as a vaccine or medication, to provoke an immune response in the body. It matters to investors because high immunogenicity can affect the effectiveness and safety of a product, potentially leading to increased costs or regulatory challenges. Understanding immunogenicity helps assess the long-term viability and market potential of pharmaceutical and biotech investments.
pandemic medical
"H5N1 - an important proof of platform capability and a recognized pandemic risk"
A pandemic is a widespread outbreak of an infectious disease that spreads across multiple countries or continents and affects large numbers of people. For investors, a pandemic matters because it can disrupt supply chains, consumer demand, workforce availability and government policy, creating sudden risks and opportunities across many industries—much like a storm that reshapes which buildings stand and which need rebuilding.
pharmacokinetic medical
"Dose-finding and pharmacokinetic/pharmacodynamic modeling to define the protective"
Pharmacokinetic describes how a drug moves through and leaves the body — how it is absorbed, spread to tissues, broken down and excreted — like tracking a package from pickup to delivery and disposal. For investors, these properties determine effective dose, safety risks, how often a medicine must be taken, and how reliably it works, which in turn influence clinical trial success, regulatory approval chances, production complexity and a drug’s commercial value.
toxicology medical
"Initiation of GLP-style toxicology and immunogenicity studies oriented toward"
Toxicology is the science that studies how chemicals, drugs or other substances can harm people, animals or the environment and determines what exposure levels are safe. For investors, toxicology results act like a safety checklist: they influence whether a product can get regulatory approval, be sold without restrictions, or face recalls and legal risks—factors that can materially affect a company’s prospects and stock value.

AI-generated analysis. Not financial advice.

OCI Collaborate 2 Commercialize Agreement Executed to Fund
Proprietary Seasonal Influenza Candidate Development

Guelph, Ontario--(Newsfile Corp. - April 14, 2026) - Zentek Ltd. (TSXV: ZEN) (NASDAQ: ZTEK) ("Zentek" or the "Company") today announces that its subsidiary Triera Biosciences Inc. ("Triera") has completed a Government of Canada contract through the Innovative Solutions Canada ("ISC") program. The project centered on the development of an aptamer-based asset for binding and deactivating H5N1, the influenza strain responsible for highly pathogenic avian influenza (HPAI). Selection of the aptamer at the center of this asset was achieved in approximately 7 weeks - a speed and adaptability profile the Company believes would not have been achievable through conventional antibody-based molecular recognition approaches. A full technical report of the results of this program will be forthcoming once all project partners have completed their final reports.

Meanwhile, based on the positive progress of the platform's development, Triera has executed an Ontario Centres of Innovation ("OCI") Collaborate 2 Commercialize ("C2C") agreement, activating the next phase of development focused on proprietary seasonal influenza treatment candidates. The total approved OCI C2C project budget is approximately $300,000, with OCI and Zentek providing matched cash contributions. The program will be conducted in collaboration with the Li and Miller Laboratories at McMaster University.

Building on the foundation provided by the recently completed H5N1 studies, Triera extended the aptamer discovery platform to seasonal influenza virus targets, applying the same multivalent aptamer engineering principles to hemagglutinin (HA) subtypes H1 and H3, without restarting discovery from first principles.

OCI C2C Agreement and Advanced Development

This phase is strategically distinct from the ISC Testing Stream scope: while the ISC contract validated the platform against highly pathogenic H5N1 - an important proof of platform capability and a recognized pandemic risk - the OCI phase is directed toward seasonal influenza strains, including H1N1 and H3N2, the two most commonly circulating Influenza A subtypes responsible for seasonal flu.1

The OCI-funded program will apply proprietary aptamer engineering methods - including the multivalent aptamer architecture established through the SARS-CoV-2 and H5N1 programs - to develop candidates with the potency profiles required for clinical advancement. Key workstreams include:

  • Advanced candidate selection and optimization using multivalent aptamer engineering for enhanced binding avidity and stability in the presence of nucleases

  • Expanded strain coverage including H1N1, H3N2 and H7N9 to demonstrate multi-subtype platform applicability

  • Dose-finding and pharmacokinetic/pharmacodynamic modeling to define the protective and therapeutic window

  • Initiation of GLP-style toxicology and immunogenicity studies oriented toward Health Canada regulatory dialogue

Management Commentary

Dr. Matthew S. Miller, Ph.D., Scientific Director, Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, and Co-Director, Canadian Pandemic Preparedness Hub, said: "Up to 20% of the global population (~1.66 billion people) are estimated to be infected with seasonal influenza viruses each year. These infections are estimated to cause 3 to 5 million cases of severe infection, and 290,000 to 650,000 deaths each year - despite the availability of seasonal influenza vaccine and antiviral drugs.2 This underscores the massive unmet medical need and market potential for developing new strategies to prevent and treat seasonal influenza virus. The evolution of our aptamer platform from SARS-CoV-2, to highly-pathogenic avian influenza H5N1, to seasonal influenza virus is logical and demonstrates the flexibility of our technology and its suitability to address ongoing challenges in infectious disease prevention."

Adam MacIntosh, Ph.D., VP of Scientific Affairs, Triera Biosciences, said: "We are proud to have been a part of such relevant and important development work with support from the federal government and in collaboration with the thorough and rigorous research teams at McMaster University, and are excited to begin the work associated with the new OCI funding. These efforts have highlighted the extreme speed and modularity of the aptamer development platform, as well as its potential role in solidifying Canada as a major proponent of foresight and preparedness for future threats from infectious disease. Triera will continue to leverage the products, knowledge, and momentum generated from these programs to deliver even greater advances in the months and years ahead."

About Triera Biosciences Ltd.

Triera holds an exclusive, worldwide, royalty-bearing license from McMaster University to use and practice aptamer applications developed through the collaboration with the Li Lab for the next 20 years. Triera and McMaster's combined expertise and capabilities in aptamer technology offer the potential to reduce the cost and time required for the development of new treatments and molecular recognition tools.

About Zentek

Zentek Ltd. is a Canadian intellectual property development and commercialization company advancing a portfolio of graphene-enabled and advanced material technologies across clean air, next-generation materials, and critical minerals. The Company's core platforms are Albany Graphite, ZenGUARD™, and Triera.

About ISC

Innovative Solutions Canada ("ISC") is a government-wide initiative that leverages procurement to connect federal departments with Canadian companies, including small and medium-sized enterprises (SMEs), and their innovative technologies.

Through the program the government launches solution-based calls to develop, test and procure Canadian innovations that address government priorities and operational needs. Funding and testing opportunities allow for Canadian-developed solutions to be refined and validated within an operational context, increasing supplier readiness and visibility for potential future adoption by federal organizations.

About OCI

The Ontario Centre of Innovation ("OCI") brings industry, academic, and government partners together to invest in collaborative R&D, technology development, and commercialization opportunities that generate the highest return on innovation for Ontarians.

As an ecosystem connector, OCI initiates unparalleled partnership opportunities, develops and manages successful industry-academic collaborations, supports high-potential SMEs in commercializing ground-breaking research, and provides hands-on training and skills development opportunities for the next generation of highly-skilled talent. OCI drives economic growth and job creation through investments in the development, commercialization, and adoption of advanced technologies.

Forward-Looking Statements

This news release contains forward-looking statements. Since forward-looking statements address future events and conditions, by their very nature they involve inherent risks and uncertainties. Although Zentek believes that the assumptions and factors used in preparing the forward-looking information in this news release are reasonable, undue reliance should not be placed on such information, which only applies as of the date of this news release, and no assurance can be given that such events will occur in the disclosed time frames or at all. Zentek disclaims any intention or obligation to update or revise any forward-looking information, whether as a result of new information, future events or otherwise, other than as required by law.

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

References:

1) Types of Influenza Viruses, Centers for Disease Control and Prevention, (https://www.cdc.gov/flu/about/viruses-types.html#:~:text=What%20to%20know,to%20cause%20illness%20in%20people.), 26 September 2025.

2) Influenza (seasonal), World Health Organization, (https://www.who.int/news-room/fact-sheets/detail/influenza-(seasonal), 25 February 2025.

For further information:

Mohammed (Moe) Jiwan
Chief Executive Officer, Zentek Ltd.
T: 416-709-8876
E: mjiwan2@zentek.com
W: www.zentek.com

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/292366

FAQ

What did Triera Biosciences (ZTEK) secure for seasonal influenza development on April 14, 2026?

Triera executed an OCI Collaborate 2 Commercialize agreement activating a seasonal influenza program. According to the company, the approved project budget is approximately $300,000 with matched cash contributions from OCI and Zentek.

How fast did Triera select an aptamer for H5N1 and why does that matter for ZTEK investors?

Triera selected an H5N1-binding aptamer in approximately 7 weeks, showing platform speed. According to the company, this rapid selection highlights adaptability versus conventional antibody approaches and supports faster candidate iteration for seasonal influenza targets.

Which influenza strains will Triera target under the OCI C2C project for ZTEK?

The OCI-funded program will target seasonal Influenza A subtypes H1N1 and H3N2, with expanded coverage including H7N9. According to the company, multivalent aptamer engineering will be applied to demonstrate multi-subtype platform applicability.

What preclinical workstreams does Triera plan next for its influenza candidates (ZTEK)?

Triera plans advanced candidate optimization, dose-finding, PK/PD modeling, and initiation of GLP-style toxicology and immunogenicity studies. According to the company, these steps are oriented toward informing Health Canada regulatory dialogue for clinical advancement.

Will Triera publish detailed results from the ISC H5N1 program and when will investors see them?

A full technical report will be published once all project partners complete their final reports. According to the company, the report is forthcoming, so investors should expect additional data after partner submissions are finalized.