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Co-Diagnostics and CoSara Advance Ebola PCR Test Development and Co-Dx™ PCR Point-of-Care Platform Capabilities

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Co-Diagnostics (Nasdaq: CODX) and joint venture CoSara reported progress in developing Ebola PCR tests and expanding the Co-Dx™ PCR point-of-care platform.

The program includes a pan-Ebola assay to detect multiple ebolavirus species and a multiplex assay to differentiate Sudan, Taï Forest, Zaire, and Bundibugyo strains, with planned point-of-care, blood-based testing on Co-Dx PCR Pro®, all subject to further development and regulatory review.

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Positive

  • Dual-assay Ebola PCR program targeting detection and differentiation of multiple ebolavirus species
  • Planned first blood-based pathogen assay for the Co-Dx PCR Pro® platform
  • Expansion of Co-Dx PCR platform beyond swab-based infectious disease testing
  • Strategy supports point-of-care deployment in outbreak and surveillance settings
  • International infrastructure via CoSara enables localized manufacturing and deployment

Negative

  • Ebola assays remain under development and require validation before use
  • All Co-Dx PCR platform components are subject to FDA and other regulatory review
  • Co-Dx PCR platform and associated tests are not yet available for sale

News Market Reaction – CODX

+0.32%
21 alerts
+0.32% News Effect
+50.4% Peak Tracked
-19.3% Trough Tracked
+$104K Valuation Impact
$32.72M Market Cap
0.1x Rel. Volume

On the day this news was published, CODX gained 0.32%, reflecting a mild positive market reaction. Argus tracked a peak move of +50.4% during that session. Argus tracked a trough of -19.3% from its starting point during tracking. Our momentum scanner triggered 21 alerts that day, indicating elevated trading interest and price volatility. This price movement added approximately $104K to the company's valuation, bringing the market cap to $32.72M at that time.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights continued expansion of the Co-Dx™ PCR point-of-care platform, including...
Analysis

This announcement highlights continued expansion of the Co-Dx™ PCR point-of-care platform, including development of pan-Ebola and multiplex assays and a potential first blood-based pathogen assay for the system. It follows multiple recent Ebola strategy updates and broader JV manufacturing build-out. Investors may monitor progress on validation, regulatory review, and deployment requirements, as well as how the platform’s menu expansion integrates with earlier initiatives in respiratory, tuberculosis, and HPV testing.

Key Figures

Announcement date: June 2, 2026
1 metrics
Announcement date June 2, 2026 Press release date for Ebola PCR and point-of-care update

Historical Context

5 past events · Latest: May 26 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 26 Ebola strategy update Positive +79.7% Advanced PCR strategy with CoSara for Bundibugyo and pan-Ebola detection.
May 19 Private placement Negative +28.4% $3.0M at-the-market private placement with common and pre-funded warrants.
May 19 Ebola assay strategy Positive +43.8% Completion of Bundibugyo virus assay strategy on Co-Dx PCR platform.
May 14 Q1 2026 earnings Negative -21.2% Low revenue, high operating expenses and net loss, plus cash update.
May 8 JV facility lease Positive +31.1% CoMira JV finalized lease for Sudair PCR manufacturing facility.

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

Pattern Detected

CODX has often seen strong upside on positive partnership and Ebola assay updates, while earnings pressure led to a notable selloff. A prior private placement saw a positive price reaction, diverging from typically negative financing sentiment.

Recent Company History

Over the past month, CODX issued several notable updates. On May 8, its CoMira JV secured a ~14,400 sq ft Saudi manufacturing site, with shares up 31.09%. Q1 2026 results on May 14 showed revenue of $0.15M and a net loss of $9.1M, followed by a -21.17% move. Subsequent Ebola assay strategy news on May 19 and May 26 drove gains of 43.8% and 79.68%, highlighting strong market sensitivity to outbreak-related platform updates, which this new Ebola PCR progress further extends.

Key Terms

pan-ebola assay, multiplex assay, point-of-care, pcr, +4 more
8 terms
pan-ebola assay medical
"development of both a pan-Ebola assay designed to rapidly detect multiple ebolavirus"
A pan-Ebola assay is a laboratory test designed to detect any species or strain of Ebola virus rather than just one type, like a smoke detector that sounds an alarm for all kinds of smoke. Investors care because broad, reliable tests are central to outbreak response, public health screening and clinical trials, which drives regulatory pathway clarity, market size and recurring demand for diagnostic providers.
multiplex assay medical
"and a multiplex assay capable of differentiating among Sudan, Taï Forest, Zaire,"
A multiplex assay is a laboratory test that measures several biological markers or targets at the same time from one sample, like scanning many items on a grocery conveyor belt in a single pass. For investors, it matters because these tests can cut time and cost, increase the amount of actionable data from each test, and improve the competitiveness and scalability of diagnostics or drug-development products, which can influence revenue, adoption, and regulatory value.
point-of-care medical
"workflow configurations also being developed to support point-of-care environments for"
"Point-of-care" refers to the location where immediate decision-making or actions happen, often involving the direct delivery of services or results. In healthcare, it describes tests or treatments performed directly at the patient's side, rather than in a distant laboratory. For investors, understanding "point-of-care" highlights the convenience, speed, and potential growth opportunities of services or products that bring solutions directly to the user or patient.
pcr medical
"Co-Diagnostics, Inc. (Nasdaq: CODX) ("Co-Dx" ), a molecular diagnostics company"
PCR (polymerase chain reaction) is a laboratory method that makes many copies of a tiny piece of genetic material (DNA or RNA) so scientists can detect and study it reliably — think of photocopying a faint, tiny note until the words are easy to read. For investors, PCR matters because it underpins diagnostic tests, drug development, and biotech tools whose sales, regulatory approvals, and real-world use can materially affect company revenues and market perceptions during health events or product launches.
blood-based pathogen assay medical
"would represent the first blood-based pathogen assay designed for use on the"
A blood-based pathogen assay is a laboratory test that looks for signs of microbes—such as bacteria, viruses, or fungi—in a person’s blood, acting like a smoke detector that signals the presence of an infection. Investors care because the test’s accuracy, speed, regulatory clearance, and insurance coverage determine how widely it can be used in hospitals and clinics, which directly affects a maker’s revenue potential, clinical adoption and long-term market value.
regulatory review regulatory
"subject to future development, validation, regulatory review, and deployment requirements."
A regulatory review is the formal evaluation by a government agency or regulator of a company’s product, filing, or business practice to confirm it meets legal, safety and disclosure requirements. For investors, the outcome and timing matter because approval can unlock sales and growth while delays, additional conditions, or rejections can limit revenue, increase costs or create legal risk—think of it like a building inspection that controls whether a project can open and under what rules.
ngos other
"supporting outbreak response efforts, including those of potential NGO partners,"
Non-governmental organizations (NGOs) are independent, not-for-profit groups that pursue social, environmental, humanitarian or policy goals outside government control. For investors they matter because NGOs can shape public opinion, press for regulation, run campaigns, or expose problems in a company’s operations or supply chain. Think of them as a public watchdog: their actions can change sales, legal costs, brand value and long-term risk, affecting investment returns.
fda regulatory
"platform ... is subject to review by the FDA and/or other regulatory bodies"
The FDA is the U.S. federal agency that evaluates and approves medical drugs, devices, biological therapies and certain foods; think of it as the gatekeeper that decides whether a medical product is safe and effective for patients. For investors, FDA decisions determine whether a company can sell a product, affect expected revenue and introduce regulatory risk, so approvals, rejections or safety warnings can quickly move a company's valuation and stock price.

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

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Dual-assay strategy designed to support outbreak response and surveillance efforts in affected regions

Potential blood-based Ebola assay would represent an important expansion of Co-Dx™ PCR point-of-care platform capabilities

SALT LAKE CITY, June 2, 2026 /PRNewswire/ -- Co-Diagnostics, Inc. (Nasdaq: CODX) ("Co-Dx" or "the Company"), a molecular diagnostics company with a unique, patented platform for the development of molecular diagnostic tests, today announced continued progress in its Ebola PCR development program with joint venture CoSara Diagnostics Pvt. Ltd. ("CoSara" or the "JV"). The program includes development of both a pan-Ebola assay designed to rapidly detect multiple ebolavirus species and a multiplex assay capable of differentiating among Sudan, Taï Forest, Zaire, and Bundibugyo ebolaviruses currently associated with outbreaks in Central Africa.

(PRNewsfoto/Co-Diagnostics)

This dual-assay strategy is intended to provide flexibility in supporting outbreak response efforts, including those of potential NGO partners, subject to future development, validation, regulatory review, and deployment requirements.

"Our ability to rapidly develop and deploy molecular diagnostic solutions for emerging infectious disease threats is one of the most important differentiators of the Co-Dx platform," said Dwight Egan, Chief Executive Officer of Co-Diagnostics. "The progress we are making with Ebola reflects not only the flexibility of our assay design capabilities, but also the value of the international infrastructure we have built through CoSara. As outbreaks emerge around the world, combining rapid assay development with localized manufacturing and deployment capabilities positions us to respond quickly when new diagnostic needs arise."

The Ebola PCR assay workflow configurations also being developed to support point-of-care environments for the Co-Dx PCR point-of-care platform* would represent the first blood-based pathogen assay designed for use on the Co-Dx PCR Pro®. This would significantly expand the platform's capabilities beyond swab-based infectious disease testing and increase the range of potential applications that may be addressed through future menu expansion.

Mr. Egan continued, "Many of the world's most serious infectious diseases are identified using blood samples, and expanding the platform to support those applications would represent an important step forward for Co-Diagnostics. The ability to bring rapid, high-quality PCR testing closer to patients, whether through respiratory, tuberculosis, HPV, or blood-borne disease applications, supports our broader goal of making molecular diagnostics more accessible in both developed and emerging markets."

*The Co-Dx PCR platform (including the PCR Home®, PCR Pro®, mobile app, and all associated tests) is subject to review by the FDA and/or other regulatory bodies and is not yet available for sale.

About Co-Diagnostics, Inc.:
Co-Diagnostics, Inc., a Utah corporation, is a molecular diagnostics company that develops, manufactures and markets state-of-the-art diagnostics technologies. The Company's technologies are utilized for tests that are designed using the detection and/or analysis of nucleic acid molecules (DNA or RNA). The Company also uses its proprietary technology to design specific tests for its Co-Dx PCR at-home and point-of-care platform (subject to regulatory review and not currently for sale) and to identify genetic markers for use in applications other than infectious disease.

Forward-Looking Statements:
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as "believes," "expects," "estimates," "intends," "may," "plans," "will," "seeks," "anticipates," and similar expressions, or the negative of these terms. Forward-looking statements in this press release include, but are not limited to, statements regarding: (i) the Company's ability to execute its assay joint development strategy for Ebolavirus tests with CoSara Diagnostics; (ii) the potential future development, validation, regulatory review, commercialization, manufacture, and distribution of the tests; (iii) the Company's ability to rapidly respond to emerging infectious disease threats; (iv) the potential utility, effectiveness, and adoption of the Co-Dx PCR platform for decentralized diagnostics and outbreak monitoring, including for blood-borne pathogens; and (v) potential collaborations with governmental and non-governmental organizations relating to infectious disease preparedness and response. Such statements are subject to a number of risks and uncertainties, including, without limitation: risks that market demand or public health conditions may change; risks related to the Company's ability to successfully develop, validate, obtain regulatory authorization or approval for, manufacture, and commercialize any Ebola assay or related products; risks related to regulatory review by the FDA or other regulatory authorities; risks related to the performance, reliability, and market acceptance of the Co-Dx PCR platform; risks associated with dependence on third parties, suppliers, collaborators, and distribution partners; risks related to competition, technological change, and intellectual property protection; and other risks described from time to time in the Company's filings with the Securities and Exchange Commission ("SEC"). Actual results may differ materially from those expressed or implied in these forward-looking statements. Readers are cautioned not to place undue reliance on forward-looking statements. A further description of risks and uncertainties can be found in the Company's Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 31, 2026, and in its other filings with the SEC. The Company undertakes no obligation to update any forward-looking statements to reflect events or circumstances after the date of this press release, except as required by applicable law.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/co-diagnostics-and-cosara-advance-ebola-pcr-test-development-and-co-dx-pcr-point-of-care-platform-capabilities-302788234.html

SOURCE Co-Diagnostics

FAQ

What did Co-Diagnostics (CODX) announce about its Ebola PCR test development on June 2, 2026?

Co-Diagnostics announced progress in its Ebola PCR development program, including dual assays for detection and strain differentiation. According to Co-Diagnostics, the work is being advanced with joint venture CoSara to support outbreak response and surveillance in affected regions.

What is the dual-assay strategy for the Co-Diagnostics (CODX) Ebola PCR tests?

The dual-assay strategy includes a pan-Ebola assay and a multiplex assay differentiating Sudan, Taï Forest, Zaire, and Bundibugyo ebolaviruses. According to Co-Diagnostics, this design aims to give flexibility for outbreak response and potential NGO partner support.

How will the Ebola PCR program affect the Co-Dx PCR Pro® point-of-care platform for CODX?

The Ebola program includes developing blood-based workflows for the Co-Dx PCR Pro®, potentially its first blood pathogen assay. According to Co-Diagnostics, this would extend platform use beyond swab-based testing into broader infectious disease applications.

Is the Co-Dx PCR point-of-care platform from Co-Diagnostics (CODX) available for sale?

The Co-Dx PCR platform, including PCR Home®, PCR Pro®, mobile app, and tests, is not yet available for sale. According to Co-Diagnostics, it remains subject to FDA and other regulatory reviews before potential commercialization.

How could Co-Diagnostics’ (CODX) Ebola PCR tests support outbreak response and surveillance?

The assays are intended to rapidly detect multiple ebolavirus species and distinguish key strains. According to Co-Diagnostics, this flexibility could aid outbreak response efforts and surveillance programs, including those of prospective NGO partners in Central Africa and other affected regions.

What broader diagnostic applications does Co-Diagnostics (CODX) target with its Co-Dx PCR platform?

Co-Diagnostics aims to support respiratory, tuberculosis, HPV, and blood-borne disease testing on its Co-Dx PCR platform. According to Co-Diagnostics, the goal is to bring rapid PCR diagnostics closer to patients in both developed and emerging markets.