Evaxion's new phase 2 data shows 86% of vaccine targets trigger tumor-specific immune responses, enhancing cancer treatment potential.
Quiver AI Summary
Evaxion A/S has announced new phase 2 data for its personalized cancer vaccine EVX-01, which shows a remarkable 86% success rate in triggering a tumor-specific immune response. This data, derived from a trial combining EVX-01 with MSD's KEYTRUDA® in patients with advanced melanoma, will be presented at the American Association for Cancer Research (AACR) Annual Meeting on April 22, 2026. The findings reinforce the effectiveness of Evaxion's AI-Immunology™ platform in accurately identifying relevant vaccine targets and indicate durable immune responses over two years. The trial has achieved a 75% Objective Response Rate alongside promising results indicating high numbers of novel tumor-specific T cells, suggesting enhanced anti-tumor efficacy. Evaxion aims to leverage these results to advance its pipeline of innovative cancer and infectious disease vaccines.
Potential Positives
- New phase 2 data shows a record-high 86% success rate of vaccine targets triggering tumor-specific immune responses, indicating a strong potential for effective cancer treatment.
- The AI-Immunology™ platform is validated as an effective tool for developing potentially transformational treatments, enhancing the company's credibility in the biotech field.
- The trial results, including a 75% Objective Response Rate, provide promising evidence of the efficacy of EVX-01 in combination with KEYTRUDA® for advanced melanoma patients.
- Presentation at the prestigious AACR Annual Meeting highlights the company’s commitment to transparency and dissemination of research findings within the scientific community.
Potential Negatives
- The press release includes a forward-looking statement that highlights uncertainties regarding the company's financial condition, need for additional capital, and the risks involved in product development and clinical trials, which may create concerns for investors.
- The reliance on third parties for clinical testing and product manufacture presents a potential risk factor that could impact the success of the company’s pharmaceutical products.
- The mention of the need for partnerships indicates potential challenges in the company's ability to advance its products in a competitive market, raising concerns about its future growth and sustainability.
FAQ
What is EVX-01?
EVX-01 is a personalized peptide-based cancer vaccine designed for treating multiple advanced solid cancers using AI-Immunology™ technology.
When will the new data be presented?
The new data will be presented at the AACR Annual Meeting on April 22, 2026, in San Diego, California.
What is the success rate of the EVX-01 vaccine?
86% of the vaccine targets in EVX-01 trigger a tumor-specific immune response, significantly higher than other methods.
What were the results of the phase 2 trial?
The phase 2 trial showed a 75% Objective Response Rate and durable immune responses over two years after administration.
How does AI-Immunology™ contribute to cancer treatment?
AI-Immunology™ accurately identifies and selects relevant vaccine targets, enhancing the development of effective cancer treatments.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$EVAX Hedge Fund Activity
We have seen 8 institutional investors add shares of $EVAX stock to their portfolio, and 3 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- POINT72 ASSET MANAGEMENT, L.P. added 33,100 shares (+inf%) to their portfolio in Q4 2025, for an estimated $157,887
- STONEPINE CAPITAL MANAGEMENT, LLC added 20,000 shares (+inf%) to their portfolio in Q4 2025, for an estimated $95,399
- RHUMBLINE ADVISERS added 11,653 shares (+123.5%) to their portfolio in Q4 2025, for an estimated $55,584
- WESBANCO BANK INC added 10,000 shares (+inf%) to their portfolio in Q4 2025, for an estimated $47,699
- IKARIAN CAPITAL, LLC removed 5,302 shares (-6.6%) from their portfolio in Q4 2025, for an estimated $25,290
- BOOTHBAY FUND MANAGEMENT, LLC removed 5,302 shares (-22.3%) from their portfolio in Q4 2025, for an estimated $25,290
- ROYAL BANK OF CANADA added 3,900 shares (+inf%) to their portfolio in Q4 2025, for an estimated $18,603
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$EVAX Analyst Ratings
Wall Street analysts have issued reports on $EVAX in the last several months. We have seen 2 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- Edward Jones issued a "Buy" rating on 10/30/2025
- Lake Street issued a "Buy" rating on 10/20/2025
To track analyst ratings and price targets for $EVAX, check out Quiver Quantitative's $EVAX forecast page.
$EVAX Price Targets
Multiple analysts have issued price targets for $EVAX recently. We have seen 4 analysts offer price targets for $EVAX in the last 6 months, with a median target of $10.0.
Here are some recent targets:
- An analyst from Jones Trading set a target price of $10.0 on 03/10/2026
- Swayampakula Ramakanth from HC Wainwright & Co. set a target price of $16.0 on 03/09/2026
- Thomas Flaten from Lake Street set a target price of $9.0 on 03/09/2026
- Soumit Roy from Edward Jones set a target price of $10.0 on 10/30/2025
Full Release
- New phase 2 data from personalized cancer vaccine EVX-01 demonstrates a record-high rate of vaccine targets triggering a tumor-specific immune response
- The results reinforce that Evaxion’s pioneering AI platform, AI-Immunology™ accurately identifies and selects the most relevant vaccine targets
-
Data will be presented at the American Association for Cancer Research (AACR) Annual Meeting
COPENHAGEN, Denmark, April 17, 2026 - Evaxion A/S (NASDAQ: EVAX) (“Evaxion”), a clinical-stage TechBio company developing novel vaccines with its pioneering AI-Immunology™ platform, announces new data demonstrating that AI-Immunology™ identifies and selects the most therapeutically relevant vaccine targets. The data will be presented at the AACR Annual Meeting in San Diego, California, on April 22, 2026.
86% of the vaccine targets included in Evaxion’s personalized cancer vaccine EVX-01 trigger a tumor-specific immune response. This is a success rate much higher than what has been reported for other methods. The high number reflects a broad yet specific immune response, increasing the likelihood of strong anti-tumor effect and positive clinical outcomes.
“We are delighted with the data demonstrating again the unique capabilities of AI-Immunology™ in identifying and selecting relevant vaccine targets. This is a further validation of the platform as an effective tool for developing potentially transformational treatments of cancer and other diseases,” says Bigitte Rønø, CSO of Evaxion.
Encouraging data
In addition to the 86% success rate, the new data set includes two-year analysis showing durable vaccine-specific immune responses following EVX-01 administration. Notably, high
de novo
responses (86%) were observed, meaning the vaccine gives rise to a high number of novel tumor specific T cells. This potentially increases the vaccine’s tumor killing ability.
Further, a positive correlation between vaccine target AI-prediction scores and the magnitude of the immune responses was demonstrated, underlining the predictive power of AI-Immunology™.
The new data stems from the phase 2 trial investigating EVX-01 in combination with MSD’s (Merck & Co., Inc., Rahway, NJ, USA) anti-PD-1 therapy, KEYTRUDA® (pembrolizumab) in patients with advanced melanoma. Each patient enrolled in the trial received a unique vaccine designed and manufactured based on their individual biology. KEYTRUDA® is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.
The trial has already yielded encouraging two-year clinical data, including a 75% Objective Response Rate. Its one-year extension was successfully completed earlier this month with three-year clinical data expected to be presented in the second half of 2026.
AACR presentation details
Abstract title: AI-designed personalized neoantigen vaccine, EVX-01, induces durable
de novo
T-cell responses in advanced melanoma patients
Poster#: 7741
Session category: Clinical research
Session title: Immune response to therapies
Location: Poster section 42
Date/Time: April 22, 2026, at 9am-12pm CST/16-19 CET
Presenter: Mads Lausen Nielsen, PhD, Project Manager at Evaxion
About EVX-01
EVX-01 is a personalized peptide-based cancer vaccine intended for first-line treatment of multiple advanced solid cancers. It is Evaxion’s lead clinical asset.
Designed with our AI-Immunology™ platform, EVX-01 and is tailored to target the unique tumor profile and immune characteristics of each patient. It engages the patient's immune system to fight off cancer by mounting a targeted response against tumors.
Contact information
Evaxion A/S
Mads Kronborg
Vice President, Investor Relations & Communication
+45 53 54 82 96
[email protected]
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 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.