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VERAXA Biotech Announces Advancement of Novel Bispecific Antibody Drug Conjugate Program VXA-222 from Joint Discovery Collaboration with OmniAb

(Very High)
(Very Positive)
Tags
partnership

VERAXA Biotech (NASDAQ: VRXA) announced that bispecific antibody-drug conjugate program VXA-222, originating from its May 2025 alliance with OmniAb (NASDAQ: OABI), has achieved a key technical milestone and is advancing into the next collaboration phase as OmniAb’s discovery work has concluded.

VXA-222 is a bispecific ADC using an “AND-gate” design to target two antigens on solid tumors in a single molecule. VERAXA used OmniAb’s transgenic antibody discovery technologies, including OmniClic, to generate antibody leads and will now apply its proprietary linker and conjugation technology, and conduct in vitro and in vivo validation. VERAXA holds exclusive development and commercialization rights to products using OmniAb-derived antibodies, while OmniAb is entitled to a share of specified revenue from such products.

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Positive

  • VXA-222 bsADC program reaches key technical milestone and advances phase
  • VERAXA secures exclusive rights to develop and commercialize OmniAb-derived products
  • OmniAb’s discovery phase completed, providing diverse antibody leads for VXA-222
  • Combination of OmniAb discovery and VERAXA linker technology establishes new candidate

Negative

  • None.

Market reaction after partnership milestone: VRXA +11.67% in the Jul 27 session

+11.67%
18 alerts
+11.67% Session close to close
+19.5% Peak Tracked
-2.1% Trough Tracked
$265.93M Market Cap
0.4x Rel. Volume

In the Jul 27 session, VRXA gained 11.67%, reflecting a significant positive market reaction. Argus tracked a peak move of +19.5% during that session. Argus tracked a trough of -2.1% from its starting point during tracking. Our momentum scanner triggered 18 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock surged +11.7% in the session following this news. On July 6, 2026, VRXA rose 7.35% after a...
Analysis

The stock surged +11.7% in the session following this news. On July 6, 2026, VRXA rose 7.35% after a business update. This partnership milestone would be read against that prior response pattern, while low short positioning provides limited evidence of squeeze-related trading; development execution remains a sourced risk.

Key Figures

Alliance established: May 2025 Target antigens: 2 target antigens Molecule format: 1 molecule
3 metrics
Alliance established May 2025 VERAXA-OmniAb joint discovery collaboration
Target antigens 2 target antigens VXA-222 AND-gate bispecific ADC
Molecule format 1 molecule VXA-222 addresses two antigens on solid tumors

Historical Context

5 past events · Latest: Jul 23 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 23 Leadership appointment Neutral -9.3% Christoph Erkel appointed Chief Scientific Officer, followed by a 9.27% negative reaction.
Jul 20 Regulatory progress Positive -2.8% PEI scientific advice supported the BiTAC-TCE development plan, followed by a 2.75% decline.
Jul 13 AI collaboration Positive -2.7% Ardigen collaboration expanded AI-enabled discovery efforts, followed by a 2.73% decline.
Jul 10 CFO appointment Neutral -2.7% Carl von Halem became interim CFO, followed by a 2.73% negative reaction.
Jul 06 Business update Positive +7.3% Pipeline and partnering strategy update preceded a 7.35% gain.

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

Pattern Detected

Recent announcements generally diverged from the stock's subsequent move, with the July 6 business update the sole aligned positive reaction.

Key Terms

bispecific adc, and-gate, affinity maturation, in vivo
4 terms
bispecific adc medical
"advancement of bispecific ADC (bsADC) program VXA-222"
A bispecific ADC is a targeted therapeutic molecule that combines a bispecific antibody—able to bind two different cellular targets—with a linked drug payload that kills cells once delivered. Think of it like a guided missile with two targeting sensors that ensure it locks onto the right cells before releasing its cargo. It matters to investors because this design can change efficacy, safety, development complexity, and commercial potential compared with single-target therapies.
and-gate technical
"VXA-222 utilizes an “AND-gate” logic"
An AND gate is a basic electronic building block that outputs a positive signal only when all of its inputs are positive, like a gate that opens only when every key in a set is turned. Investors care because AND gates are fundamental to chips and digital systems; their design, manufacturing yield and performance affect a semiconductor maker’s product competitiveness, production costs and revenue potential, much like a reliable engine affects a carmaker’s sales and margins.
affinity maturation medical
"naturally optimized through in vivo affinity maturation"
Affinity maturation is the immune-system process where B cells evolve to produce antibodies that bind more tightly and specifically to a target, through rounds of mutation and selection in specialized lymph node areas. For drug and vaccine development, stronger and more specific antibodies often indicate a more effective or durable immune response, so affinity maturation is a measurable sign researchers use to compare and optimize therapeutic or vaccine candidates, much like refining a tool until it fits precisely.
in vivo technical
"responsible for in vitro and in vivo validation"
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.

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

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VXA-222 advances into next phase at VERAXA

ZURICH, SWITZERLAND, July 27, 2026 -- VERAXA Biotech AG (NASDAQ: VRXA; “VERAXA” or the "Company"), an emerging leader in designing novel cancer therapies, today announced the advancement of bispecific ADC (bsADC) program VXA-222, following successful achievement of a key technical milestone in its alliance with OmniAb, Inc. (NASDAQ: OABI, “OmniAb”). The program is moving into its next collaboration phase with OmniAb's discovery work successfully concluded. VXA-222 utilizes an “AND-gate” logic to address two different target antigens present on solid tumors with one molecule. Established in May 2025, the alliance and joint discovery collaboration brought together OmniAb’s cutting-edge suite of transgenic antibody discovery solutions and screening technologies with VERAXA’s proprietary antibody drug conjugate (ADC) linker technology and conjugation expertise to support next-generation therapeutic discovery.

“We are pleased to announce this important achievement and the advancement of this program from our alliance with OmniAb for the development of a novel AND-gated bsADC utilizing our conjugation and linker technology,” commented Christoph Erkel, Ph.D., Chief Scientific Officer of VERAXA. “This successful partnership has united two highly complementary technologies to establish a new therapeutic candidate in VXA-222, representing a powerful opportunity for a best-in-class bispecific ADC to address solid tumor indications with high unmet medical need. We look forward to advancing this program and acknowledge OmniAb’s partnership and contributions in delivering a diverse set of highly promising antibodies.”

Under the terms of the May 2025 agreement, VERAXA initiated a novel bsADC program addressing two attractive target molecules in cancer medicine. The Company utilized OmniAb's suite of transgenic antibody discovery solutions, including OmniClic™, a common light-chain transgenic chicken developed to facilitate the generation of bispecific antibodies, to source high-quality human antibody leads, which are naturally optimized through in vivo affinity maturation. VERAXA will subsequently establish the bsADC lead candidate by applying its proprietary linker technology and conjugation routine and will be responsible for in vitro and in vivo validation. VERAXA holds exclusive rights to develop and commercialize products incorporating the OmniAb-derived antibodies under the collaboration, with OmniAb entitled to a share of specified revenue generated from those products.

“We’re delighted to see this bispecific ADC program cross this important threshold,” said Bill Harriman, Ph.D., Senior Vice President of Discovery Partnership Management and Technology Development and Operations at OmniAb. “Continuation of the discovery phase at VERAXA underscores the productive collaboration and alliance between our scientific and business teams, and highlights the complementary strengths of OmniAb’s technologies and VERAXA’s expertise in ADC conjugation and development. We look forward to seeing our partners at VERAXA advance this exciting program.”


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.

BiTAC® is a registered trademark of VERAXA Biotech GmbH.


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, including the advancement of the Company’s collaborative development program with OmniAb, its anticipated pipeline development focus, its ability to monetize its pipeline assets, the timing for development of its pipeline candidates, the potential therapeutic benefits of its pipeline candidates and the ability of the company to partner its pipeline assets. 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 in 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 most recent Annual Report on Form 20-F and any subsequent reports on Form 6-K. 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.


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
investors@veraxa.com

Attachment


FAQ

What did VERAXA Biotech (VRXA) announce about its VXA-222 program on July 27, 2026?

VERAXA Biotech announced that its bispecific ADC program VXA-222 reached a key technical milestone and moved into the next collaboration phase. According to VERAXA, OmniAb’s discovery work is complete, and VERAXA will now lead bsADC candidate establishment and preclinical validation activities.

What is VXA-222 in VERAXA Biotech’s (VRXA) oncology pipeline?

VXA-222 is a bispecific antibody-drug conjugate that applies an “AND-gate” logic to target two antigens on solid tumors with one molecule. According to VERAXA, it aims to create a best-in-class bsADC for solid tumor indications with high unmet medical need.

How are VERAXA Biotech (VRXA) and OmniAb (OABI) collaborating on the VXA-222 bsADC program?

VERAXA and OmniAb formed a joint discovery alliance in May 2025, combining OmniAb’s transgenic antibody discovery technologies with VERAXA’s ADC linker and conjugation expertise. According to VERAXA, OmniAb generated human antibody leads and VERAXA will now establish and validate the bsADC lead candidate.

What technology platforms are used in VERAXA Biotech’s VXA-222 bispecific ADC program?

VXA-222 uses OmniAb’s transgenic antibody discovery suite, including the OmniClic common light-chain chicken, to generate bispecific antibody leads. According to VERAXA, these are combined with its proprietary ADC linker technology and conjugation processes to create next-generation antibody-based cancer therapeutics.