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VERAXA Biotech Establishes in vitro Proof-of-Concept for Novel BiTAC-ADC Technology Platform and Launches Partnering Discussions at BIO International Convention 2026

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VERAXA Biotech (NASDAQ: VRXA) reported in vitro proof-of-concept data for its novel BiTAC-ADC technology, showing selective, dose-dependent killing of breast cancer cells and 3D tumor spheroids while sparing healthy cells. The company will seek partnering opportunities for its BiTAC-ADC and BiTAC-TCE platforms at BIO International 2026.

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News Market Reaction – VRXA

-23.55%
16 alerts
-23.55% Session close to close
+8.9% Peak Tracked
-25.0% Trough Tracked
$961.22M Market Cap
147.37K Volume

In the Jun 18 session, VRXA declined 23.55%, reflecting a significant negative market reaction. Argus tracked a peak move of +8.9% during that session. Argus tracked a trough of -25.0% from its starting point during tracking. Our momentum scanner triggered 16 alerts that day, indicating notable trading interest and price volatility.

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BiTAC-ADC in vitro data, along with initial data from the most advanced BiTAC-TCE program recently presented at the American Association for Cancer Research (AACR) Annual Meeting, underpin the Company’s two viable and clearly differentiated product platform technologies

ZURICH, SWITZERLAND – June 18, 2026 -- VERAXA Biotech AG (NASDAQ: VRXA; “VERAXA”), an emerging leader in designing novel cancer therapies, today announced that the Company has generated new in vitro proof-of-concept data validating its novel BiTAC-ADC technology platform and its potential to enable more precise and targeted cancer therapies. VERAXA will attend the BIO International Convention in San Diego, Calif., June 22-25, 2026, to discuss partnering opportunities based on its novel BiTAC-ADC and BiTAC-TCE platforms.

The BiTACTM therapeutic strategy is designed to unlock a new level of precision in cancer treatment by using two complementary precursors and enabling a tumor-restricted activation of the desired therapeutic effect. Applied to the development of antibody drug conjugates (ADCs), the technology delivers a systemically inactive prodrug and a cell-impermeable proactivator through two separate antibodies, each addressing a defined tumor-associated antigen. While the single BiTAC-ADC precursors are therefore not toxic by design, the selective internalization of both components into the same cancer cells leads to dose-dependent cytotoxicity. In in vitro studies, BiTAC-ADCs have now been shown to discriminate between breast cancer and healthy cells and have demonstrated efficient and dose-dependent killing of 3D tumor cell spheroids.

“Following our successful listing on NASDAQ earlier this month, the BIO International Convention presents a great opportunity and is the ideal timing to provide more details on how our BiTAC-ADC platform can be applied to the potential benefit of cancer patients,” said Heinz Schwer, Ph.D., MBA, Chief Business Officer of VERAXA. “Current ADC technologies have transformed cancer treatment but continue to face challenges associated with off-tumor toxicity caused by payload exposure in healthy tissues. BiTAC-ADCs are specifically designed to address this issue. By doing so, the platform could allow the use of very potent payloads in more settings than previously possible, with the ambition of improving both safety and targeted efficacy of next-generation ADC therapeutics.”

“While still early in development, the data now available for our BiTAC-ADC platform indicate that our concept of selectively delivering and activating a toxic payload in tumor cells is working,” said Christoph Erkel, Ph.D., Vice President Research & Development at VERAXA. “Following the presentation of our BiTAC-TCE strategy at the recent AACR Annual Meeting in April, these novel datasets on the BiTAC-ADC platform underpin that the company has two viable and clearly differentiated product platform technologies, which can be applied in a range of solid tumor indications by us and our potential future partners.”


About VERAXA Biotech AG (NASDAQ: VRXA)

At VERAXA, we are building a premier engine for the discovery and development of next-generation antibody-based therapeutics, including bispecific T cell engagers, bispecific ADCs and other innovative formats. Powered by a suite of transformative technologies and guided by rigorous quality-by-design principles, we are rapidly advancing our pipeline of ADCs and proprietary BiTAC formats into clinical development and beyond. VERAXA was founded on scientific breakthroughs made at the European Molecular Biology Laboratory (EMBL), a world-renowned institution known for pioneering life science research and cutting-edge technology.

For regular updates about VERAXA Biotech, visit https://investors.veraxa.com/ or follow us on LinkedIn, X (formerly known as Twitter) and Bluesky.


Forward-looking Statements

This press release may contain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. All statements that address activities, events, or developments that VERAXA Biotech AG (the "Company") intends, expects, plans, projects, believes, or anticipates will or may occur in the future are forward-looking statements. Such forward-looking statements are based on current expectations and involve inherent risks and uncertainties, including factors that could delay, divert or change any of them, and could cause actual outcomes and results to differ materially from current expectations. No forward-looking statement can be guaranteed. Forward-looking statements contained on this press release should be evaluated together with the many uncertainties that affect the Company's business, particularly those identified in the risk factors section of the Company’s registration statement on Form F-4. These documents are available from the Securities and Exchange Commission, the Company website or from Company Investor Relations.

In addition, any information contained in this press release was current as of the date presented and should not be relied upon as representing our estimates as of any subsequent date. While we may elect to update forward-looking statements at some point in the future, we specifically disclaim any obligation to do so, even if our estimates change, whether as a result of new information, future events or otherwise. Consequently, the company will not update the information contained in this press release and investors should not rely upon the information as current or accurate after the presentation date. The press release may also contain certain non-GAAP financial measures, adjusted to exclude certain costs, expenses, gains and losses and other specified items. Reconciliations of these non-GAAP financial measures to the most comparable GAAP measures for a particular quarterly period are available on the Company’s website at www.veraxa.com.​​​


Contact

VERAXA Biotech AG - Corporate
Christoph Antz, Ph.D.
Chief Executive Officer, Co-Founder
investors@veraxa.com

For Media and Investors – U.S.
Brandon Weiner
ICR Healthcare
VERAXA@icrhealthcare.com

For Media and Investors – EU
Mario Brkulj
media@veraxa.com

Attachment


FAQ

What BiTAC-ADC proof-of-concept did VERAXA Biotech (NASDAQ: VRXA) announce on June 18, 2026?

VERAXA announced in vitro proof-of-concept data validating its novel BiTAC-ADC technology platform. According to VERAXA, BiTAC-ADCs discriminated between breast cancer and healthy cells and induced efficient, dose-dependent killing of 3D tumor cell spheroids, supporting the platform’s potential for targeted cancer therapy.

How does VERAXA Biotech's BiTAC-ADC technology aim to improve antibody drug conjugates for VRXA investors?

BiTAC-ADC uses two complementary antibody-based precursors to restrict toxic payload activation to tumor cells. According to VERAXA, the systemically inactive prodrug and cell-impermeable proactivator become cytotoxic only when both are internalized into the same cancer cells, aiming to enhance tumor selectivity.

What partnering discussions will VERAXA Biotech (VRXA) pursue at BIO International Convention 2026?

VERAXA plans to discuss partnering opportunities for its BiTAC-ADC and BiTAC-TCE platforms at BIO International 2026. According to VERAXA, these differentiated product platform technologies may be applied across a range of solid tumor indications in collaboration with potential future partners.

How could BiTAC-ADCs address off-tumor toxicity seen with current ADC technologies for VERAXA (VRXA)?

BiTAC-ADCs are designed to limit payload activation to tumor cells, potentially reducing off-tumor toxicity. According to VERAXA, separating a prodrug and proactivator across two antibodies aims to avoid payload exposure in healthy tissues while enabling use of very potent cytotoxic payloads.

What is the relationship between VERAXA's BiTAC-ADC and BiTAC-TCE platforms for VRXA shareholders?

VERAXA positions BiTAC-ADC and BiTAC-TCE as two viable, differentiated product platforms based on its BiTAC strategy. According to VERAXA, recent BiTAC-TCE data and new BiTAC-ADC in vitro results together support applications across multiple solid tumor indications and potential collaborations.

What stage of development is VERAXA Biotech's BiTAC-ADC platform as of June 2026?

The BiTAC-ADC platform is at an early development stage, supported by in vitro proof-of-concept data. According to VERAXA, current datasets show selective delivery and activation of a toxic payload in tumor cells, but no clinical data are reported in this announcement.