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The technology

Exhauvir- Endless antiviral assets

EXHAUVIR is an innovative therapeutic molecule built from two synergistic parts. The first binds with high specificity and affinity to all strains of a virus’s genetic material, triggering natural cellular mechanisms that destroy the virus—without leaving harmful residues. The second acts as a built-in safety and regulation system, minimizing off-target effects that may occur due to the molecule’s high thermal stability, ensuring maximum efficacy with uncompromised safety.

EXHAUVIR offers a unique set of advantages: it is unaffected by viral mutations, can be easily shipped and stored at room temperature, and cannot be translated into proteins. Our molecule binds with exceptionally high affinity compared to RNA or DNA oligos, ensuring robust antiviral activity. With our platform, the molecule can be rapidly adapted to any existing virus or newly emerging viral threat. In-vitro studies across different cell types demonstrated 97.1% protection from virus-induced death. To date, we have developed therapeutic molecules targeting viral respiratory diseases, multiple herpes strains, and measles. Antiviral therapies also reduce long-term risks such as virus-driven cancers or future damages. While our immediate focus is antiviral, the same platform has the potential to expand into oncology and rare genetic disorder- applications already secured within our IP portfolio.

AI & Bioinformatics tools

At Viritis, we believe the future of medicine relies on speed, precision, and adaptability. Our AI-driven platform, powered by the NVIDIA Inception Program and the Google Cloud Startup Program, drastically reduces antiviral development by scanning the entire viral genome to identify the genes essential for the virus’s survival.

Within these genes, we focus on conserved regions that are long enough to activate the cell’s natural defenses yet short enough to be synthesized efficiently. These regions are carefully selected to ensure they do not interfere with cellular functions. We also analyze potential viral mutations to design molecules that remain effective even as the virus evolves.

This unique approach allows us to create safe, mutation-resistant treatments that can be rapidly adapted to any virus—accelerating development, lowering costs, and providing powerful protection against both current and emerging viral threats.

Conserved region in Cytomegaloviruses (CMV)

Unfair advantage

97.1% Cellular protection

  • High stability
  • Safety- minimal side effects
  • Virtually no toxicity

Faster Drugs Development process

  • AI Algorithms for faster target identification
  • AI Algorithms for safety prediction
  • Customizable lead molecule

No cold chain required

  • Extended Shelf Life
  • Lyophilized Shipments
  • Improved Storage & Transport
  • Rapid Reconstitution

Faster regulatory pathway

  • Pharma companies could use the (505b2) pathway to get FDA approval for each new drug in 12 months
  • We Conduct only preclinical studies (no need for FDA approval)