Pre-seed · Antiviral CRISPR platform

Design safe antiviral CRISPR tools
for any virus — fast.

CRISPRGuard is a smart program that helps scientists create antiviral CRISPR designs. Upload virus genomes, find conserved targets, and verify safety against the human genome.

Talk to founders See results
100%
Human-genome safe candidates
≥95%
Filovirus subgroup coverage
4,344
Human DENV genomes (of 4,850)
$60B+
Antiviral market (2024)

Many viruses still have no real cure

For pathogens like dengue, rabies, and herpes, medicine mostly offers vaccines or lifelong symptomatic treatment — not targeted, designable antivirals that keep up with mutations.

CRISPRGuard: universality + safety by design

An online platform with a simple interface and working code. Upload virus genomes and mutations — get conserved targets, positions, and human-safety checks in a ready table.

🧬

Any virus genome

Works across viral families — including hard-to-treat pathogens where classic drugs fall short.

🛡️

Human-safe guides

Every candidate sequence is checked against the human genome. Safety is a first-class filter, not an afterthought.

Fast research loop

From NCBI multi-genome input to ranked gRNA tables — built for chemists and biotech teams who need speed.

CRISPR-Cas9 / Cas13b + LNP delivery

Guides designed by CRISPRGuard feed into a known modality stack: mRNA-encoded Cas, guide RNA, and lipid nanoparticle (or similar) delivery — aligned with clinical CRISPR precedents.

In the body

A tablet or injection delivers a lipid envelope with CRISPR-Cas mRNA and guide RNA. Inside the cell, mRNA is translated; Cas binds the guide and forms a complex that can stay active for an extended stability window (up to ~10 days). If a virus enters in that window, viral nucleic acid is cut before replication.

Why now

First CRISPR medicines are already approved (e.g. Casgevy). In vivo LNP programs such as NTLA-2001 and related trials show deep target knockdown in humans — the delivery and safety story for CRISPR is no longer theoretical.

Real genome-scale results

We are not only a slide deck — the pipeline has been run on major human-pathogenic virus sets.

Ebola + Marburg — pan-filovirus gRNAs

Targeting all human-transmitted strains across Zaire, Sudan, Bundibugyo, Bombali, and Marburg subgroups.

  • NCBI genomes screened 803 → 622 core
  • Universal 10-gRNA combo ≥95% coverage
  • Sudan ebolavirus 100% with 2 gRNAs
  • Human off-target check 100% safe

Human-transmissible DENV

NCBI Virus dengue set analyzed for Cas13b guide targets: 4,850 genomes total, of which 4,344 are human-associated strains.

  • Genomes in set (total → human) 4,850 → 4,344
  • Exact multi-site matches 3,800–4,100
  • Near-exact coverage 95%
  • Multi-gRNA projection 98%

Antivirals are a growing category

Governments and pharma already spend billions on pandemic prep — but universal design tools remain underinvested.

$60B+

Global antiviral drug market value in 2024

$127B

Projected market size by 2035

$3.2B

Example: U.S. HHS investment in oral COVID antivirals

How we get paid

Compute-as-service for institutes, partnerships with DNA-therapy pharma, and IP share on real drugs.

Round

Pre-seed — $300K · Target path via Trendlines and strategic pharma / CRISPR ecosystem partners (Pfizer, Roche/Genentech, Novartis, Gilead, Moderna, Intellia, Mammoth, BARDA/CEPI-class orgs, and others).

Founders

Young chemists and builders, guided by PhD-level science.

VS

Valentin Stefashin

CEO · Co-founder

Bio-Technology student. Leads product vision, platform, and company building.

IP

Irina Peres

Co-founder · Head of Product

Owns product direction and partner-facing execution.

AK

Artur Kudrin, Ph.D.

Chemistry Expert

Scientific guidance on chemistry and experimental rigor.

Building the design layer for antiviral CRISPR

Looking for research partners, pilot genome projects, and pre-seed investors. Happy to walk through the pipeline, filovirus / dengue results, and roadmap.