PTAP™ | Programmable CRISPR Antivirals
Pharmaceutical Products, Prescriptions
Information
Seek Labs’ Programmable Target Ablation Platform (PTAP™) is a CRISPR-based therapeutic system designed to rapidly generate antivirals across human and animal health. PTAP targets essential pathogen genetic sequences to irreversibly disrupt replication, offering a precise and adaptable alternative to traditional antivirals and vaccines.
PTAP development is powered by BioSeeker™, Seek Labs’ machine learning engine that analyzes pathogen genomic data to identify conserved, high-impact targets with low mutation risk. This approach enables rapid design of pathogen-specific and pan-pathogen therapeutics and compresses early discovery and development timelines from years to months.
In human health, PTAP programs include pan-Orthopox (Smallpox and Mpox), pan-Influenza A, pan-Dengue (serotypes 1–4), pan-RSV, and beta-coronaviruses including SARS-CoV-2 and MERS. The pipeline is expanding into hemorrhagic fevers and other priority indications aligned with pandemic preparedness, outbreak response, zoonotic spillover, neglected tropical diseases, and government stockpiling initiatives.
PTAP supports multiplexed targeting, allowing a single therapeutic to address multiple strains or species within a viral family. This design improves durability and reduces resistance driven by viral evolution. Programs are modular and reprogrammable, enabling rapid response to emerging threats across geographies and hosts.
In animal health, PTAP has demonstrated in vivo efficacy against African Swine Fever Virus (ASFV), a lethal disease with no approved treatment. Additional programs include Capripoxvirus (Lumpy Skin Disease, Goatpox, Sheeppox) and Classical Swine Fever Virus (CSFV), with expansion underway into companion animal health. These programs address food security, economic resilience, and zoonotic risk at the human–animal interface.
PTAP™ is an investigational therapeutic platform currently in preclinical development. Not cleared or approved by the FDA or any other regulatory autho
