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Revolutionizing PRRSV Control: The Bivalent CS20 Vaccine.

Tailored, internationally patented, and dual-action protection against Type 1 & Type 2 PRRSV.

Addressing a $2B annual global farming cost with innovative, reprogrammable vaccine technology.

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Vaccine Production Line

The Ongoing Global Burden of PRRSV

PRRSV remains one of the most economically damaging infectious diseases affecting the global swine industry, contributing to billions in annual losses through respiratory disease, reproductive failure, mortality, reduced growth performance, and increased production costs.

Economic Impact

PRRSV is estimated to cost the global pork industry more than $2 billion annually through decreased productivity, treatment costs, and herd instability.

Rapid Viral Evolution

The continuous mutation and co-circulation of both Type 1 and Type 2 PRRSV strains create major challenges for long-term disease control and vaccine efficacy.

High Production Losses

Outbreaks can result in:

  • Increased piglet mortality

  • Severe respiratory disease

  • Reproductive failure in breeding herds

  • Reduced average daily gain

  • Elevated veterinary intervention costs

Cross-Strain Vulnerability

Conventional monovalent vaccines often provide limited cross-protection against genetically diverse or emerging PRRSV strains, leaving herds vulnerable to reinfection and production disruption.

Vaccine

Introducing the CS20 Bivalent PRRSV Vaccine Platform

CS20 has been designed to address the growing complexity of PRRSV control through a dual-action vaccine strategy capable of targeting both major PRRSV genotypes simultaneously.

Bivalent Protection

Simultaneous targeting of both Type 1 and Type 2 PRRSV strains through a single vaccine platform engineered for broader immune coverage.

Reprogrammable Technology

The CS20 platform has been developed with future adaptability in mind, enabling rapid tailoring to emerging PRRSV variants and evolving regional disease pressures.

International Patent Position

The vaccine platform is supported by international intellectual property protection, strengthening its commercial and strategic licensing potential.

Commercial Relevance

Designed to support large-scale global deployment through partnership with established animal health manufacturers and commercial distributors.

Vaccine

Advancing Through Controlled Challenge Studies

Current development activities are focused on generating a comprehensive efficacy and safety data package through controlled live pig challenge studies designed to support future regulatory submissions and global licensing discussions.

Safety Evaluation

Assessment parameters include:

  • Reduction in viremia

  • Reduced viral shedding

  • Local tolerance assessment

  • Monitoring for adverse clinical responses

  • Evaluation of overall production performance

Efficacy Evaluation

Challenge studies are designed to demonstrate:

  • Reduced respiratory disease severity

  • Lower lung lesion scores

  • Reduced rectal temperature elevation

  • Lower viral load following heterologous challenge

  • Broader protection across genetically diverse strains

Tailored Vaccine Capability

Additional studies are evaluating the platform’s ability to be adapted toward regionally relevant and emerging PRRSV lineages, including highly pathogenic variants circulating in Asia.

What our customers are saying

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