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Evaxion announces business update and second quarter 2026 financial results

(Positive)
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Evaxion (NASDAQ: EVAX) reported second quarter 2026 results and a business update. Net loss was $3.7 million, compared with $3.6 million in Q1 2026 and $4.8 million in Q2 2025. R&D expenses were $2.3 million and G&A expenses $1.5 million, both broadly stable versus Q1 and with lower G&A than a year earlier.

Cash and cash equivalents totaled $14.0 million at June 30, 2026, supporting a cash runway into the second half of 2027. The company advanced its AI-Immunology™-derived pipeline, including upcoming three‑year data for personalized cancer vaccine EVX‑01, new preclinical data for off‑the‑shelf cancer vaccines EVX‑04 and EVX‑05, and CMV vaccine candidate EVX‑V1. Evaxion also received the 2026 Prix Galien UK Award for Best digital health solution.

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Positive

  • Net loss reduced YoY to $3.7M in Q2 2026 from $4.8M in Q2 2025
  • G&A expenses down to $1.5M in Q2 2026 from $2.2M in Q2 2025
  • Net financial expense fell to $0.1M from $0.7M in Q2 2025
  • Cash runway funded into second half of 2027 with $14.0M cash
  • Multiple pipeline advances including EVX‑01, EVX‑04, EVX‑05 and EVX‑V1 data readouts and preparations for EVX‑04 clinical filing
  • External platform validation via 2026 Prix Galien UK Award for AI‑Immunology™

Negative

  • Ongoing losses with Q2 2026 net loss of $3.7M and H1 2026 net loss of $7.4M
  • No revenue reported in Q2 2026 versus $37K in Q2 2025
  • Cash balance decline to $14.0M at June 30, 2026 from $23.2M at December 31, 2025
  • Total equity decreased to $9.5M at June 30, 2026 from $17.0M at year‑end 2025

Market Context

The May 7, 2026 earnings event produced a -7.71% reaction despite pipeline progress and runway guida...
Analysis

The May 7, 2026 earnings event produced a -7.71% reaction despite pipeline progress and runway guidance. Against that record, this release adds financial detail; declining equity and ongoing losses remain relevant risks.

Key Figures

Net loss: $3.7 million R&D expenses: $2.3 million G&A expenses: $1.5 million +5 more
8 metrics
Net loss $3.7 million Q2 2026, compared with $3.6 million in Q1 2026 and $4.8 million in Q2 2025
R&D expenses $2.3 million Q2 2026
G&A expenses $1.5 million Q2 2026, compared with $2.2 million in Q2 2025
Net financial expense $0.1 million Q2 2026, compared with $0.7 million in Q2 2025
Cash and cash equivalents $14.0 million As of June 30, 2026; runway confirmed into the second half of 2027
Total equity $9.5 million As of June 30, 2026, compared with $17.0 million as of December 31, 2025
Loss per share -$0.01 Q2 2026 basic and diluted, compared with -$0.02 in Q2 2025
Shares used for calculation 417,010,756 Q2 2026 basic and diluted

Previous Earnings Reports

5 past events · Latest: May 07 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 07 Q1 earnings report Positive -7.7% Pipeline progress and extended cash runway accompanied quarterly financial results.
Mar 05 FY2025 earnings report Positive +9.3% Partnership licensing, clinical data, milestones, and improved financial position were reported.
Nov 06 Q3 earnings report Positive +10.6% Leadership change, clinical data, licensing proceeds, and extended runway highlighted results.
Aug 14 Q2 earnings report Positive -5.9% Trial progress, grant recognition, debt conversion, and improved quarterly loss were reported.
May 27 Q1 earnings report Positive +25.5% Clinical progress, improved cash position, and potential partnership catalysts accompanied results.

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

Pattern Detected

Evaxion's earnings announcements showed mixed outcomes, with three positive and two negative subsequent price reactions despite generally constructive updates.

Key Terms

phase 2, neoantigens, endogenous retrovirus, in vivo, +1 more
5 terms
phase 2 medical
"We completed the initially planned two-year treatment in the phase 2 trial"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
neoantigens medical
"EVX-01 is designed to target multiple neoantigens"
Neoantigens are new protein fragments that appear on the surface of diseased cells, most often cancer cells, because of changes in their DNA; the immune system can recognize these as foreign. For investors, neoantigens matter because they are targets for precision therapies and vaccines that aim to teach the immune system to attack only diseased cells—think of them as unique fingerprints that enable treatments to be more specific and potentially more effective, which can drive clinical and commercial value.
endogenous retrovirus medical
"EVX-04 targets multiple non-conventional endogenous retrovirus (ERV) tumor antigens"
Endogenous retroviruses are remnants of ancient viral infections that became permanently embedded in an organism’s DNA and are inherited across generations, like fossilized viruses inside the genome. They can turn genes on or off or produce viral-like proteins, so they matter to investors because they are potential targets or safety liabilities for diagnostics, therapies and vaccines, influencing research value, regulatory review and clinical outcomes.
in vivo medical
"specific immune responses both in mice (in vivo) and human cells"
In vivo describes tests or experiments performed inside a living organism, such as an animal or human, to observe how a drug, device or biological process behaves in a real, functioning body. Investors care because in vivo results reveal safety, effectiveness and possible side effects that lab tests cannot, much like road-testing a prototype car in traffic rather than only on a bench — outcomes can strongly influence regulatory approval, clinical success and a company’s valuation.
in vitro medical
"specific immune responses both in mice (in vivo) and human cells (in vitro)"
In vitro describes laboratory tests performed on cells, tissues, or biological molecules outside a living body—literally “in glass,” such as in test tubes or dishes. For investors, in vitro results are an early sign that a drug or technology has a desired effect under controlled conditions, but they don’t guarantee it will work or be safe in animals or people; think of them as a prototype tested on a bench rather than in real-world use.

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

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COPENHAGEN, Denmark, August 20, 2026 - Evaxion A/S (NASDAQ: EVAX) (“Evaxion”), a clinical-stage TechBio company developing novel vaccines with its pioneering AI-Immunology™ platform, provides business update and announces second quarter 2026 financial results.

Business highlights (since last quarterly update)
Evaxion is making steady progress towards completing its strategic milestones for 2026. Highlights include:

  • Announcing the upcoming presentation of three-year clinical data for personalized cancer vaccine candidate EVX-01 at the ESMO Congress 2026
  • Presentation of new data for EVX-04, an off-the-shelf cancer vaccine for acute myeloid leukemia (AML)
  • Expansion and refocusing of our R&D pipeline with EVX-05, a novel off-the-shelf therapeutic cancer vaccine program for glioblastoma
  • Presentation of new data for cytomegalovirus (CMV) vaccine candidate EVX-V1
  • Winning the 2026 Prix Galien UK Award for Best digital health solution for AI-Immunology™
  • Cash runway unchanged with cash at hand to fund operations into the second half of 2027

“Progress remains strong in recent months, particularly regarding the expansion and progression of our R&D pipeline. Both EVX-04 and EVX-05 represent completely new concepts in targeting hard-to-treat cancers and are great examples of what we can do with AI-Immunology™ to identify novel, conserved cancer targets for off-the-shelf vaccines. The same is true for EVX-V1 in the infectious disease space and we are excited by the successful progress of this next-generation, multi-component CMV-vaccine program. These programs and the combined R&D pipeline show how our AI-Immunology™ platform can truly deliver product candidates, which is crucial in validating our platform and for partnerships,” says Helen Tayton-Martin, CEO of Evaxion.

Conference call and webcast
Evaxion’s executive management will host a conference call and webcast at 8.30 ET/14.30 CET today, presenting the business update and financial results as well as taking questions.

To join the conference call, listen to the presentation and ask verbal questions, please register in advance via this link to receive the dial-in telephone numbers and a unique PIN code. The call can be accessed 15 minutes prior to the start of the live event.

To join the webcast, please click on this link. The webcast recording will be available on our website shortly after the event.

Research & Development (R&D) update
Evaxion has a R&D pipeline of innovative vaccine candidates for both cancer and infectious diseases. In future, this is expected to be supplemented by programs for autoimmune diseases following application of AI-Immunology™ in this space in the second half of 2026.

We are looking forward to presenting three-year clinical efficacy data for personalized cancer vaccine EVX-01, our most advanced pipeline asset, at the European Society for Medical Oncology (ESMO) Congress 2026 in October.

Developed with AI-Immunology™, EVX-01 is designed to target multiple neoantigens; cancer unique proteins arising from mutations. We completed the initially planned two-year treatment in the phase 2 trial with EVX-01 in patients with advanced melanoma (skin cancer) last year with unprecedented results presented at ESMO in 2025.

Following on with a one-year extension of the phase 2 trial, the upcoming data will provide additional insights into potentially enhanced treatment effects and durability of the EVX-01-induced immune response. It will also offer insights into the vaccine’s effect also as stand-alone treatment of these patients with advanced melanoma, in comparison to the prior administration in combination with pembrolizumab in the first two years of the trial.

In addition to the personalized approach, we are leveraging AI-Immunology™’s capabilities to develop novel off-the-shelf cancer vaccines, including EVX-04 targeting AML. Developed with AI-Immunology™, EVX-04 targets multiple non-conventional endogenous retrovirus (ERV) tumor antigens from the dark genome.

ERV antigens are present in tumors but absent in normal tissue, making them highly attractive targets for cancer vaccines. AI-Immunology™ has unique capabilities in identifying ERVs and this opens a whole new source of antigens, which can potentially greatly improve patient outcomes.

We are progressing preclinical activities with EVX-04 as planned and presented new data at the European Hematology Association (EHA) 2026 Congress. The data demonstrates EVX-04’s complete expression in human cells, including correct transcription and translation. Further, EVX-04 is secreted in human cells, enabling immune recognition and activation.

The data also shows that all ERV antigens included in EVX-04 drive specific immune responses both in mice (in vivo) and human cells (in vitro) across different human immune profiles. These vaccine-induced immune cells mediate targeted cell-killing, highlighting EVX-04’s potential as a new effective therapeutic cancer vaccine.

In parallel with preclinical studies, we are preparing the regulatory filing for clinical testing of EVX-04, which is expected to be submitted before the end of the year.

We have also leveraged our capabilities to identify clinically relevant ERVs to expand our pipeline with EVX-05, a novel off-the-shelf cancer vaccine candidate for the deadly brain cancer glioblastoma.

Partly based on data analysis done in collaboration with leading experts from Duke University School of Medicine, EVX-05 targets endogenous retrovirus (ERV)-derived antigens shared between glioblastoma patients. The use of such antigens could potentially be highly effective for glioblastoma patients, who generally have few neoantigens to target due to low mutational burden.

We also carry out preclinical activities for infectious disease programs and presented new data for CMV vaccine program EVX-V1 at the International Herpesvirus Workshop 2026 in July. EVX-V1 is a next-generation, multi-component CMV vaccine program designed with AI-Immunology™. It combines novel AI-Immunology™ identified protective B-cell antigens and T-cell epitopes complemented by known optimized structural B-cell antigens.

This broader multi-targeted strategy is expected to strengthen the protective potential of a future vaccine. The concept represents a scalable strategy for rational vaccine development across other herpesviruses. The new data demonstrates the potential to improve control of acute infection, latency, and viral reactivation, further supporting the concept behind EVX-V1.

Business development update
We remain active in several parallel partnership discussions based on external interest in both our AI-platform and R&D pipeline as we continue to pursue our strategy of strengthening our platform and building value through multiple partnerships.

We were honored to receive the Prix Galien UK Award for Best digital health solution for AI-Immunology™ in June. The award is another strong external validation and recognition of the AI-Immunology™ platform and as such supporting our partnering efforts, alongside the new data we continuously generate to further validate the fact that AI-Immunology™ is a platform that deliver product candidates. This is an important proposition to potential business partners.

Second quarter 2026 financial results
The financial results for the second quarter 2026 were in line with expectations with a net loss of $3.7 million, compared to $3.6 million in the first quarter 2026 and $4.8 million in the second quarter 2025. The reduced loss compared to same period last year primarily relates to lower capital market transaction costs and financial expenses from significantly reduced derivative liability.

Research and development (R&D) expenses were $2.3 million for the second quarter 2026, aligned with first quarter 2026, and a slight increase compared to second quarter last year, as we progress our pipeline according to plan.

General and administrative (G&A) expenses were $1.5 million for the quarter, which was at same level with first quarter 2026, and compared to $2.2 million in second quarter 2025. Compared to last year the reduced cost is primarily driven by lower capital market costs.

Net financial expense of $0.1 million for the second quarter 2026 compared to net financial expense of $0.7 million same quarter last year, a reduction of net expense mainly due to reduced derivative liability and the thereof related remeasurement.

Cash and cash equivalents as of June 30, 2026, were $14.0 million, compared to $18.4 million as of March 31, 2026, and confirm our current cash runway until second half of 2027.

Total equity amounts to $9.5 million as of June 30, 2026, reflecting the net loss of the first six months of 2026 when compared to $17.0 million as of December 31, 2025.


Evaxion A/S
(Unaudited) Consolidated statement of financial position data
(USD in thousands)

  Jun 30,
2026
Dec 31,
2025
Cash and cash equivalents 14,00023,234
Total assets 19,38028,408
Total liabilities 9,84911,369
Share capital 15,79115,791
Other reserves 127,343127,492
Accumulated deficit (133,603)(126,244)
Total equity 9,53117,039
Total liabilities and equity 19,38028,408


Evaxion A/S
(Unaudited) Consolidated statement of comprehensive loss data
(USD in thousands, except per share data)

 Three Months Ended
June 30,
Six Months Ended
June 30,
 2026202520262025
Revenue-37-37
Research and development(2,334)(2,165)(4,631)(4,321)
General and administrative(1,512)(2,212)(3,034)(3,924)
Operating loss(3,846) (4,340)(7,665) (8,208)
Finance income1475464054,305
Finance expenses(234)(1,232)(519)(2,895)
Net loss before tax(3,933) (5,026)(7,779) (6,798)
Income tax benefit204195420387
Net loss for the period(3,729) (4,831)(7,359) 6,411
Net loss attributable to shareholders of Evaxion A/S(3,729) (4,831)(7,359) 6,411
Loss per share – basic and diluted(0.01)(0.02)(0.02)(0.02)
Number of shares used for calculation (basic and diluted)417,010,756315,828,608417,010,756275,434,522


Contact information 
Evaxion A/S
Mads Kronborg
Vice President, Investor Relations & Communication
+45 53 54 82 96
mak@evaxion.ai

About Evaxion
Evaxion is a pioneering TechBio company based upon its proprietary, clinically validated and scalable AI platform, AI-Immunology™. The platform harnesses the power of artificial intelligence to decode the human immune system and develop novel vaccine candidates for cancer and infectious diseases.        

With AI-Immunology™ we conduct rapid, efficient and high-quality target discovery, drug design and development. Our team of +40 experts covers the entire value chain from target discovery to clinical development

We have developed a clinical pipeline of both personalized and off-the-shelf cancer vaccine candidates as well as prophylactic vaccine candidates for infectious diseases. All our candidates address high unmet medical needs, reflecting our commitment to transforming patients’ lives by providing innovative and targeted treatment options.

For more information about Evaxion, AI-Immunology™ and our pipeline, please visit our website

Forward-looking statement 
This announcement contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. The words “target,” “believe,” “expect,” “hope,” “aim,” “intend,” “may,” “might,” “anticipate,” “contemplate,” “continue,” “estimate,” “plan,” “potential,” “predict,” “project,” “will,” “can have,” “likely,” “should,” “would,” “could,” and other words and terms of similar meaning identify forward-looking statements. Actual results may differ materially from those indicated by such forward-looking statements as a result of various factors, including, but not limited to, risks related to: our financial condition and need for additional capital; our development work; cost and success of our product development activities and preclinical and clinical trials; commercializing any approved pharmaceutical product developed using our AI platform technology, including the rate and degree of market acceptance of our product candidates; our dependence on third parties including for conduct of clinical testing and product manufacture; our inability to enter into partnerships; government regulation; protection of our intellectual property rights; employee matters and managing growth; our ADSs and ordinary shares, the impact of international economic, political, legal, compliance, social and business factors, including inflation, and the effects on our business from other significant geopolitical and macro-economic events; and other uncertainties affecting our business operations and financial condition. For further discussion of these risks, please refer to the risk factors included in our most recent Annual Report on Form 20-F and other filings with the US Securities and Exchange Commission (SEC), which are available at www.sec.gov. We do not assume any obligation to update any forward-looking statements except as required by law. 


FAQ

What were Evaxion (NASDAQ: EVAX) key financial results for Q2 2026?

Evaxion reported a Q2 2026 net loss of $3.7 million, with R&D expenses of $2.3 million and G&A expenses of $1.5 million. According to Evaxion, results were in line with expectations and reflected lower capital market and financial costs versus the prior year.

How much cash does Evaxion (EVAX) have and what is its cash runway after Q2 2026?

Evaxion reported $14.0 million in cash and cash equivalents as of June 30, 2026. According to Evaxion, this balance supports its current operating plans and confirms an expected cash runway extending into the second half of 2027, assuming continued execution of its strategy.

How did Evaxion's Q2 2026 results compare to Q2 2025 for EVAX shareholders?

Evaxion's Q2 2026 net loss of $3.7 million improved from $4.8 million in Q2 2025. According to Evaxion, the smaller loss mainly reflects lower capital market transaction costs and reduced financial expenses from a significantly lower derivative liability compared with the prior‑year quarter.

What are the latest pipeline updates for Evaxion's EVX-01 cancer vaccine as of Q2 2026?

Evaxion plans to present three‑year clinical efficacy data for EVX‑01 at ESMO Congress 2026. According to Evaxion, this follows completion of a two‑year phase 2 melanoma trial and a one‑year extension, aiming to show durability and potential stand‑alone vaccine effects.

What progress did Evaxion (EVAX) report on EVX-04 and EVX-05 cancer vaccines in Q2 2026?

Evaxion advanced preclinical work on EVX‑04 for AML and introduced EVX‑05 for glioblastoma. According to Evaxion, EVX‑04 showed ERV‑targeted immune responses, and the company expects to submit a regulatory filing for EVX‑04 clinical testing before the end of 2026.

What did Evaxion announce about its CMV vaccine candidate EVX-V1 in the second quarter of 2026?

Evaxion presented new data on EVX‑V1, its next‑generation multi‑component CMV vaccine program, in July 2026. According to Evaxion, the data support improved control of acute infection, latency, and viral reactivation, reinforcing the AI‑designed multi‑target concept behind EVX‑V1.

Did Evaxion (EVAX) receive any external recognition for its AI-Immunology platform in 2026?

Evaxion received the 2026 Prix Galien UK Award for Best digital health solution for its AI‑Immunology™ platform. According to Evaxion, this award provides external validation of the platform and supports its ongoing business development and partnering discussions with potential collaborators.