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Evaxion announces business update and full year 2024 financial results

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Evaxion Biotech (NASDAQ: EVAX) reported its full year 2024 financial results and business updates. The company's partnership with MSD on two vaccine candidates is progressing towards potential option exercise in H2 2025. Their lead asset EVX-01, a personalized cancer vaccine, showed promising one-year interim data with a 69% Overall Response rate.

Financial highlights include revenue of $3.3 million in 2024 (vs $0.1M in 2023), reduced net loss of $10.6 million (vs $22.1M in 2023), and successful capital raising of approximately $17 million in early 2025. R&D expenses decreased to $10.5 million from $11.9 million in 2023.

Key 2025 milestones include two-year clinical efficacy readout for EVX-01, potential MSD option exercise worth up to $10 million, selection of lead ERV-based precision cancer vaccine candidate, and at least two new business development agreements.

Evaxion Biotech (NASDAQ: EVAX) ha riportato i risultati finanziari e gli aggiornamenti aziendali per l'intero anno 2024. La partnership dell'azienda con MSD su due candidati vaccinali sta progredendo verso un potenziale esercizio dell'opzione nel secondo semestre del 2025. Il loro principale asset, EVX-01, un vaccino personalizzato contro il cancro, ha mostrato dati intermedi promettenti a un anno con un tasso di risposta globale del 69%.

Tra i punti salienti finanziari ci sono ricavi di 3,3 milioni di dollari nel 2024 (rispetto a 0,1 milioni di dollari nel 2023), una perdita netta ridotta a 10,6 milioni di dollari (rispetto a 22,1 milioni di dollari nel 2023) e un successo nella raccolta di capitali di circa 17 milioni di dollari all'inizio del 2025. Le spese per R&S sono diminuite a 10,5 milioni di dollari da 11,9 milioni di dollari nel 2023.

I principali traguardi per il 2025 includono la lettura dell'efficacia clinica a due anni per EVX-01, un potenziale esercizio dell'opzione da parte di MSD del valore di fino a 10 milioni di dollari, la selezione del principale candidato vaccinale di precisione basato su ERV e almeno due nuovi accordi di sviluppo commerciale.

Evaxion Biotech (NASDAQ: EVAX) reportó sus resultados financieros y actualizaciones comerciales para el año completo 2024. La asociación de la empresa con MSD en dos candidatos a vacunas está avanzando hacia un posible ejercicio de opción en la segunda mitad de 2025. Su activo principal, EVX-01, una vacuna personalizada contra el cáncer, mostró datos interinos prometedores de un año con una tasa de respuesta global del 69%.

Los aspectos financieros destacados incluyen ingresos de 3,3 millones de dólares en 2024 (frente a 0,1 millones en 2023), una pérdida neta reducida de 10,6 millones de dólares (frente a 22,1 millones en 2023) y una exitosa recaudación de capital de aproximadamente 17 millones de dólares a principios de 2025. Los gastos en I+D disminuyeron a 10,5 millones de dólares desde 11,9 millones en 2023.

Los hitos clave para 2025 incluyen la lectura de eficacia clínica a dos años para EVX-01, un posible ejercicio de opción de MSD por un valor de hasta 10 millones de dólares, la selección del candidato a vacuna de precisión basado en ERV y al menos dos nuevos acuerdos de desarrollo comercial.

Evaxion Biotech (NASDAQ: EVAX)는 2024년 전체 재무 결과 및 사업 업데이트를 보고했습니다. 회사는 MSD와 두 개의 백신 후보에 대한 파트너십을 통해 2025년 하반기에 잠재적인 옵션 행사로 나아가고 있습니다. 그들의 주요 자산인 EVX-01, 개인 맞춤형 암 백신은 1년 간의 중간 데이터에서 69%의 전체 반응률을 보여주었습니다.

재무 하이라이트에는 2024년 수익이 330만 달러 (2023년 10만 달러 대비), 순손실이 1060만 달러로 감소 (2023년 2210만 달러 대비), 2025년 초에 약 1700만 달러의 자본 조달 성공이 포함됩니다. 연구 및 개발 비용은 2023년 1190만 달러에서 1050만 달러로 감소했습니다.

2025년 주요 이정표에는 EVX-01에 대한 2년 임상 효능 결과, 최대 1000만 달러의 MSD 옵션 행사 가능성, ERV 기반 정밀 암 백신 후보의 선택, 그리고 최소 두 개의 새로운 사업 개발 계약이 포함됩니다.

Evaxion Biotech (NASDAQ: EVAX) a publié ses résultats financiers et ses mises à jour commerciales pour l'année complète 2024. Le partenariat de l'entreprise avec MSD concernant deux candidats vaccins progresse vers un exercice potentiel de l'option au deuxième semestre 2025. Leur principal actif, l'EVX-01, un vaccin personnalisé contre le cancer, a montré des données intermédiaires prometteuses d'un an avec un taux de réponse global de 69%.

Les faits saillants financiers incluent des revenus de 3,3 millions de dollars en 2024 (contre 0,1 million de dollars en 2023), une perte nette réduite à 10,6 millions de dollars (contre 22,1 millions de dollars en 2023) et une levée de fonds réussie d'environ 17 millions de dollars au début de 2025. Les dépenses de R&D ont diminué à 10,5 millions de dollars contre 11,9 millions de dollars en 2023.

Les principales étapes de 2025 comprennent la lecture de l'efficacité clinique sur deux ans pour l'EVX-01, un exercice potentiel de l'option MSD d'une valeur allant jusqu'à 10 millions de dollars, la sélection du candidat vaccin de précision basé sur l'ERV, et au moins deux nouveaux accords de développement commercial.

Evaxion Biotech (NASDAQ: EVAX) hat seine finanziellen Ergebnisse und Geschäftsupdates für das gesamte Jahr 2024 veröffentlicht. Die Partnerschaft des Unternehmens mit MSD zu zwei Impfstoffkandidaten schreitet auf einen möglichen Optionsausübung im zweiten Halbjahr 2025 zu. Ihr Hauptprodukt EVX-01, ein personalisierter Krebsimpfstoff, zeigte vielversprechende einjährige Zwischenwerte mit einer Gesamtansprechrate von 69%.

Zu den finanziellen Höhepunkten gehören Einnahmen von 3,3 Millionen Dollar im Jahr 2024 (gegenüber 0,1 Millionen Dollar im Jahr 2023), ein reduzierter Nettoverlust von 10,6 Millionen Dollar (gegenüber 22,1 Millionen Dollar im Jahr 2023) und eine erfolgreiche Kapitalbeschaffung von etwa 17 Millionen Dollar Anfang 2025. Die F&E-Ausgaben sanken von 11,9 Millionen Dollar im Jahr 2023 auf 10,5 Millionen Dollar.

Wichtige Meilensteine für 2025 umfassen die zweijährige klinische Wirksamkeitsauswertung für EVX-01, eine mögliche MSD-Optionsausübung im Wert von bis zu 10 Millionen Dollar, die Auswahl des führenden präzisionsbasierten Krebsimpfstoffkandidaten und mindestens zwei neue Geschäftsentwicklungsvereinbarungen.

Positive
  • Significant revenue increase to $3.3M in 2024 from $0.1M in 2023
  • Strong interim EVX-01 trial results with 69% Overall Response rate
  • Successful $17M capital raise extending cash runway to mid-2026
  • Net loss reduced by 52% to $10.6M in 2024 from $22.1M in 2023
  • Strategic partnership with MSD progressing towards potential $10M option fee
Negative
  • Negative equity position of $1.7M as of December 31, 2024
  • Delay in expanding business development collaborations due to failed partnership discussion
  • Outstanding EIB loan of €7M requiring partial conversion to equity
  • Operating loss of $14.7M for 2024

Insights

Evaxion's 2024 financial results represent a significant improvement over the previous year, with $3.3 million in revenue (vs $0.1 million in 2023) and a substantially reduced net loss of $10.6 million (vs $22.1 million). This positive financial trajectory stems primarily from their MSD (Merck) partnership, which is tracking toward potential option exercise in H2 2025 that could trigger up to $10 million in fees.

The company has strengthened its balance sheet through successful capital raises, bringing in approximately $17 million in January 2025 and extending runway through mid-2026. Cost discipline is evident with R&D expenses down to $10.5 million (from $11.9 million) and G&A expenses reduced to $7.6 million (from $10.4 million). Importantly, management projects maintaining 2025 cash burn at approximately $14 million despite increased activities.

The pending conversion of €3.5 million of EIB debt to equity would significantly improve Evaxion's balance sheet structure by reducing liabilities and increasing equity by $3.7 million. With multiple potential value-driving catalysts in 2025 (including two-year clinical data for EVX-01 and possible MSD option exercise), Evaxion appears well-positioned financially to execute its multi-partner strategy while maintaining operational efficiency.

Evaxion's AI-Immunology™ platform continues to demonstrate its versatility and value across multiple therapeutic areas. Their phase 2 trial with personalized cancer vaccine EVX-01 has completed dosing with encouraging one-year interim results showing 69% overall response rate and 15/16 patients experiencing tumor reduction. The two-year efficacy readout expected in H2 2025 represents a significant catalyst.

The company's strategic expansion into ERV-based precision cancer vaccines marks an important diversification beyond personalized approaches. By targeting non-conventional endogenous retrovirus antigens that are shared across patients, this approach could potentially offer broader applicability while maintaining precision.

On the infectious disease front, the MSD collaboration on both EVX-B2 (Gonorrhea) and EVX-B3 validates their platform's capability in bacterial vaccine development. The enhanced AI platform with toxin antigen prediction capabilities further strengthens their competitive position in this space.

The pipeline progression across multiple modalities (personalized cancer vaccines, shared antigen precision vaccines, and infectious disease vaccines) demonstrates the platform's robustness. With two new infectious disease candidates planned for 2025, lead candidate selection for the ERV program, and advancement of their CMV vaccine program, Evaxion is effectively leveraging its AI technology to build a diversified pipeline with multiple partnership opportunities.

COPENHAGEN, Denmark, April 1, 2025 - Evaxion Biotech A/S (NASDAQ: EVAX) (“Evaxion”), a clinical-stage TechBio company specializing in developing AI-Immunology™ powered vaccines, provides business update and announces full year 2024 financial results.

Business highlights
2024 and the first months of 2025 saw Evaxion make substantial progress in both business development, research and development and financing. Key highlights are listed below.

  • Our transformational partnership with MSD (Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA) on two vaccine candidates for infectious diseases entered in September 2024. The projects are tracking according to the agreed plans towards potential option exercise in the second half of 2025.
  • The continued progression of the phase 2 trial with our lead asset, personalized cancer vaccine EVX-01, demonstrating convincing one-year interim data and on track for two-year clinical efficacy readout in the second half of 2025. The data package will be further strengthened - at low cost - through a one-year extension of the trial.
  • We also strengthened our pipeline of cancer vaccines by obtaining preclinical Proof-of-Concept for our novel precision cancer vaccine concept targeting non-conventional endogenous retrovirus (ERV) tumor antigens shared across patients. We are advancing the program at full speed towards identifying a lead vaccine candidate in the second half of 2025.
  • Our leading AI-Immunology™ platform was further improved with the launch of a novel toxin antigen predictor allowing for the development of improved bacterial vaccines. This has served to further strengthen our value proposition towards potential partners.
  • Our financial position was significantly strengthened by successfully completing a public offering in January 2025. Coupled with other capital markets activities, we brought in a net total of approximately $17 million in cash and equity, extending our cash runway to mid-2026. MSD Global Health Innovation Fund, MSD’s venture arm, remain our largest shareholder having participated in our last three equity offerings and now holds an ownership stake of just below 20%.

“Evaxion has made significant progress over the past 15 months and the company has never been stronger fundamentally. We maintain our strong momentum in strategy execution and have already achieved our first 2025 company milestone with the completion of dosing in the EVX-01 phase 2 trial in January. Having demonstrated our ability to derive value from both our AI-Immunology™ platform and our pipeline, we continue our efforts to create long-term value based on our multi-partner strategy. We are confident in our ability to deliver on our 2025 milestones focusing on business development, our platform and pipeline and in doing so further driving long-term value creation,” says Christian Kanstrup, CEO of Evaxion.

2025 milestones
Building on the many achievements we are pursuing several value catalysts for 2025. Evaxion’s strategic milestones for 2025 reflect our high activity level, broad pipeline and strong external interest in potential partnerships around both our AI-Immunology™ platform and pipeline assets. As such, the milestones underscore our continued anticipated strategic progress.

Evaxion’s overriding priorities are execution upon our business development strategy, continuation of the ongoing EVX-01 phase 2 trial, the ongoing strengthening of our AI-Immunology™ platform and further advancement of our research activities, including progressing our ERV-based precision vaccine concept towards clinical development. Finally, the focus is on bringing the MSD collaboration to option exercise.

We maintain strict cost control and diligently prioritize and optimize our resource allocation. This enables us to absorb the increased level of activity in 2025 within the same cash spend as in 2024, e.g. we expect an operational cash burn of ~$14 million in 2025.

 Milestones Target 
AI-Immunology™Launch of automated lead vaccine candidate design moduleH2
Business development and partnershipsAt least two new agreements2025
EVX-01All patients completed EVX-01 dosingH1 ✓ 
EVX-01Supplemental phase 2 biomarker and immunogenicity dataH1  
EVX-01Two-year phase 2 clinical efficacy readoutH2
Precision ERV cancer vaccinesSelection of lead vaccine candidateH2
MSD vaccine collaboration (EVX-B2/EVX-B3)MSD option exercise, up to USD 10 million option exercise feeH2
EVX-V1Lead antigens selected for CMV vaccine candidateH2
Infectious diseasesTwo new pipeline candidates1 in H1, 1 in H2


Research & Development update

We are seeing good progress across our pipeline of development programs in both cancer and infectious disease.

The phase 2 trial with EVX-01, a personalized cancer vaccine currently being evaluated as a treatment for advanced melanoma (skin cancer), is tracking nicely towards two-year clinical efficacy readout. Dosing of all patients was completed in January 2025 and the trial will yield multiple data readouts in 2025 with new biomarker and immune data to be presented at the American Association for Cancer Research (AACR) Annual Meeting taking place in Chicago April 25-30, 2025.

In the second half of the year, we are looking forward to present two-year data from the trial. Based on the convincing data obtained so far - one-year data showed a 69% Overall Response rate and 15 out of 16 patients having tumor reductions - we are eagerly awaiting the two-year readout. We are also excited to have added a one-year extension to the trial, which will at low cost strengthen EVX-01’s data package further.

Beyond personalized cancer vaccines, our AI-Immunology™ platform has also enabled us to establish an ERV-based precision cancer vaccine concept. ERVs hold a great therapeutic potential and with AI-Immunology™ we can design broadly applicable precision vaccines harnessing this potential. We expect to identify the lead candidate for this program in the second half of 2025. This will be an important milestone as we expand our pipeline of potential truly novel cancer treatments with potential broad applicability. As previously communicated, we plan to bring the vaccine candidate into early clinical development ourselves.

Our infectious disease pipeline also saw good progress. The initial collaboration with MSD on EVX-B3 was expanded to also include our proprietary pipeline candidate EVX-B2 for Gonorrhea through the option and license agreement entered in September 2024. The programs are tracking as planned towards expected option exercise in the second half of 2025. Following potential option exercise, MSD will take over further development and commercialization with Evaxion entitled to significant milestone payments as development successfully progresses. Evaxion will also receive royalties on sales if and when one or both vaccine candidates reaches the market.

We expect to utilize AI-Immunology™ to identify two new vaccine candidates for infectious diseases in 2025, the first already in the first half of the year. This will broaden our infectious disease pipeline with new assets that could potentially be partnered out like EVX-B2. Continuing to expand the pipeline with novel assets targeting significant unmet needs will be an important enabler for a continued successful execution of our multi-partner strategy.

One such already existing asset is EVX-V1, a novel vaccine program for the treatment of cytomegalovirus (CMV). We presented positive preclinical data from the program in November 2024 and are advancing these new findings to identify lead antigens for a multi-component CMV vaccine candidate in the second half of 2025. The collaboration with ExpreS2ion on EVX-V1 has been ended on their initiative, and we now hold all rights to this asset and can potentially out-license it at our discretion.

The continued development and improvement of AI-Immunology™ remain a cornerstone of our strategy to ensure our position as a leading AI-based TechBio company. In 2024, we improved the platform through an update of its EDEN™ AI prediction model. Among other improvements, the model can now predict toxin antigens, allowing for the development of improved bacterial vaccines.

This year, we expect to expand the platform with the launch of an automated lead vaccine candidate design module, among other improvements. This would further enhance the platform’s speed and accuracy in designing novel vaccines.

Business development update
Evaxion seek to generate value from both our platform and pipeline through novel target discovery collaborations as well as licensing agreements around existing pipeline assets with multiple partners. The MSD deal collaboration entered in 2024, including both a target discovery collaboration (EVX-B3) and an existing pipeline asset (EVX-B2), is a great example of the partnering strategy we are pursuing.

We continue to see a good level of external interest in our platform and pipeline and are advancing multiple partnership discussions in parallel. We have, however, seen a delay in the expansion of our business development collaborations as a potential agreement in late-stage discussions carried into 2025 has turned out not to materialize due to a late change in focus with the potential partner.

Such is the nature of business development; however, we remain encouraged by the breadth of our business development pipeline and are diligently pursuing our 2025 objective of entering into at least two new business development agreements. In parallel with advancing new potential collaborations, we of course also have a strong focus on bringing the MSD EVX-B2/EVX-B3 collaboration to potential option exercise in the second half of 2025.

EIB loan conversion
Evaxion remains in advanced discussion with the European Investment Bank (EIB) about conversion of €3.5 million out of Evaxion’s €7 million loan with EIB into an equity-type instrument. While the overall scope and objective have been agreed, final and detailed discussions are ongoing, and final documentation still needs to be agreed. The conversion is now expected to be formally finalized in the second quarter of 2025.

The conversion is expected to increase Evaxion’s equity by $3.7 million (€3.5 million) immediately upon completion. We have no debt besides the EIB-loan, so the conversion would also substantially reduce our overall liabilities, simplify our balance sheet and improve our financial flexibility and cash flow.

Full year 2024 financial results
Cash and cash equivalents as of December 31, 2024, was $6.0 million, as compared to $5.6 million as of December 31, 2023. Including the successful capital markets initiatives in January 2025, we expect that our existing cash and cash equivalents will be sufficient to fund our operating expenses and capital expenditure requirements until mid-2026.

Revenue of $3.3 million was recognized for the full year 2024, as compared to $0.1 million for 2023. The improved revenue for 2024 relates to the signed option and license agreement with MSD.

Research and development (R&D) expenses were $10.5 million for the year 2024, compared to $11.9 million for 2023. The decrease year-over-year relates to reduced headcount in R&D and cost efficiencies.

General and administrative expenses were $7.6 million for 2024, compared to $10.4 million for 2023. The decrease was primarily driven by full year saving effect in 2024, following changes to executive management in 2023. Furthermore, cost reductions related to overhead and professional fees have been realized.

For the full year 2024 we generated a net loss of $10.6 million, or $(0.20) per basic and diluted share, as compared to a net loss of $22.1 million, or $(0.81) per basic and diluted share for the year 2023. The decreased loss was driven by the recognized revenue and reduced spending in both our R&D and general & administrative expenses.

Total equity amounts to $(1.7) million as December 31, 2024.

Evaxion Biotech A/S
Consolidated Statement of Financial Position Data
(USD in thousands)

Dec 31,
2024
Dec 31,
2023
Cash and cash equivalents5,9525,583
Total assets12,48512,889
Total liabilities14,13717,618
Share capital10,5165,899
Other reserves106,36999,946
Accumulated deficit(118,537)(107,860)
Total equity before derivative warrant liability(1,652)(2,015)
Effect from derivative liabilities from investor warrants-(2,714)
Total equity(1,652)(4,729)
Total liabilities and equity12,48512,889


Evaxion Biotech A/S
Consolidated Statement of Comprehensive Loss Data
(USD in thousands, except per share data)

Three Months Ended December 31,Twelve Months Ended December 31,
2024202320242023
Revenue122733,34473
Research and development(2,255)(2,298)(10,457)(11,916)
General and administrative(1,891)(2,139)(7,619)(10,354)
Operating loss(4,024)(4,364)(14,732)(22,197)
Finance income5785596,500963
Finance expenses(458)(895)(3,123)(1,681)
Net loss before tax(3,904)(4,700)(11,355)(22,915)
Income tax benefit275177788790
Net loss for the period(3,629)(4,523)(10,567)(22,125)
Net loss attributable to shareholders of Evaxion Biotech A/S(3,629)(4,523)(10,567)(22,125)
Loss per share – basic and diluted(0.07)(0.17)(0.20)(0.81)
Number of shares used for calculation (basic and diluted)53,644,48327,335,82953,644,48327,335,829


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

About EVAXION
Evaxion Biotech A/S is a pioneering TechBio company based upon its AI platform, AI-Immunology™. Evaxion’s proprietary and scalable AI prediction models harness the power of artificial intelligence to decode the human immune system and develop novel immunotherapies for cancer, bacterial diseases, and viral infections. Based upon AI-Immunology™, Evaxion has developed a clinical-stage oncology pipeline of novel personalized vaccines and a preclinical infectious disease pipeline in bacterial and viral diseases with high unmet medical needs. Evaxion is committed to transforming patients’ lives by providing innovative and targeted treatment options. For more information about Evaxion and its groundbreaking AI-Immunology™ platform and vaccine 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 a 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's (EVAX) key financial results for 2024?

Evaxion reported revenue of $3.3M, net loss of $10.6M ($0.20 per share), R&D expenses of $10.5M, and cash position of $6.0M as of December 31, 2024.

What are the interim results of Evaxion's EVX-01 cancer vaccine trial?

EVX-01 showed a 69% Overall Response rate in one-year interim data, with 15 out of 16 patients experiencing tumor reductions.

What is the expected timeline for MSD's option exercise on Evaxion's vaccine candidates?

MSD's option exercise for EVX-B2 and EVX-B3 vaccine candidates is expected in the second half of 2025, with potential fees up to $10 million.

How long will Evaxion's current cash runway last after the January 2025 financing?

Following the $17 million raised in January 2025, Evaxion's cash runway is expected to extend until mid-2026.
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