Ardigen partners with VERAXA on AI for cancer drug discovery
Ardigen and VERAXA Biotech are teaming up to use AI and computational biology to improve target-pair selection for VERAXA’s BiTAC cancer therapies. The collaboration is aimed at speeding development of conditionally active T cell engagers and ADCs while reducing toxicity risk.
Why it matters: - The collaboration is designed to improve how VERAXA selects cancer target pairs for therapies that need to hit tumor cells without harming healthy tissue. - Better target selection could widen the therapeutic window for T cell engagers and antibody-drug conjugates, two drug classes often limited by off-tumor toxicity. - The work could help VERAXA advance its BiTAC pipeline with more precise therapeutic design and fewer late-stage failures.
What happened: - Ardigen S.A. announced a collaboration with VERAXA Biotech AG on July 13, 2026. - The partnership focuses on advancing VERAXA’s growing BiTAC® pipeline of T cell engagers and antibody-drug conjugates. - Ardigen will develop AI-enabled tools and models to help identify synergistic cancer target pairs for VERAXA’s BiTAC platform. - VERAXA said the collaboration is a strategic step to help bring precision oncology therapies to patients faster.
The details: - Ardigen will contribute expertise in computational biology, machine learning, bioinformatics and scalable data systems. - Ardigen brings 11 years of experience in those areas to the collaboration. - The companies plan to use AI to integrate and interpret complex biomedical data for therapeutic design. - VERAXA’s BiTAC-TCEs and future BiTAC-ADCs use Boolean “AND-gate” logic. - The BiTAC approach requires co-expression of two distinct targets on the same cancer cell for activation. - VERAXA says that design could spare healthy tissues and reduce systemic toxicity. - VERAXA aims to use preclinical and clinical data already generated across the industry, including data from programs that had promising efficacy but were limited by toxicity. - AI-enabled analysis is intended to help identify improved dual-target combinations, refine therapeutic design and test target-pair hypotheses more precisely. - Michał Warchoł, Ardigen’s CTO, said the collaboration will apply Ardigen’s AI, bioinformatics and computational biology solutions to improve target-pair selection. - Christoph Antz, VERAXA’s CEO and co-founder, said smart cancer target selection and thorough validation from the outset can have a major impact on future success rates and product profiles.
Between the lines: - The deal reflects a broader push in drug discovery to use AI earlier in the pipeline, before expensive experimental work narrows the field. - VERAXA’s focus on dual-target logic signals an effort to solve a common problem in potent cancer drugs: efficacy often rises as safety becomes harder to manage. - Ardigen’s role suggests VERAXA wants outside computational support, not just internal modeling, to strengthen decision-making around complex target biology.
What's next: - Ardigen and VERAXA will build AI tools and models for target-pair selection within the BiTAC platform. - The companies will use integrated biomedical data to evaluate dual-target hypotheses and refine candidate selection. - VERAXA said the collaboration should help guide the development strategy for its proprietary BiTAC programs. - Ardigen’s website is here and VERAXA’s website is here.
Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.
Sign up for:
World Healthcare Report
The daily local news briefing you can trust. Every day. Subscribe now.
Check Your Email!
We sent a one-time activation link to: .
Confirm it's you by clicking the email link.
If the email is not in your inbox, check spam or try again.
Welcome back!
is already signed up. Check your inbox for updates.