Off-The-Shelf Vaccines designed around what the immune system actually sees

Right Targets

Measured, not predicted

Our Precision Immunomics™ discovery pipeline integrates
state-of-the art immunopeptidomcs, transcriptomoics and genomics, with AI/ML trained on data from real patient samples, to produce a best-in-class repertoire of shared, tumour-specific antigens.

We detect antigens from coding and ‘dark’ regions of the genome without bias, allowing us to select the best possible targets, regardless of the source. Shortlisted targets undergo rigorous biological validation to allow us to design de-risked, off-the-shelf vaccines, cancer type by cancer type.

Close-up of a beige layered mattress showing detailed woven texture and foam padding.

Everything we see is a real target.

Using immunopeptidomics, we directly read what tumours present to the immune system.

Molecular structure of a membrane protein embedded in a spherical cell membrane.
T CELL
Illustration of a eukaryotic cell featuring a nucleus, rough endoplasmic reticulum, and Golgi apparatus.
Blue DNA double helix with a metallic lightning bolt striking through it.
3D illustration of a DNA double helix with a chemical structure overlay.
3D illustration of a DNA double helix strand with twisting structure.
Detailed 3D rendering of a green protein molecule with a twisted ribbon structure.
3D illustration of a DNA double helix structure in blue.
3D illustration of a purple DNA double helix strand.
Four colored molecular chains resembling proteins with spherical segments connected in a wavy pattern.
Antigen DNA
Orange hand-drawn arrow pointing diagonally up and to the right.
Yellow spherical beads arranged in a chain wrapping around a gray irregularly shaped object, with a separate short chain of beads nearby.
Purple caterpillar with a yellow head on a black background.
Antigen peptide
Curved orange arrow pointing to the right.
Illustration of a cell with two ribosomes attached to the endoplasmic reticulum, one purple and one blue with yellow molecules, showing protein synthesis.
MHC binding &
presentation
CANCER CELL
Orange curved arrow pointing upward and to the right.
Orange curved arrow pointing upward to the right.

Most mutations are never processed, presented, or recognised by T cells so relying on prediction restricts the proportion of identified antigens that are therapeutically relevant.

Everything we see is a real target.

Using immunopeptidomics, wedirectly read what tumours present to the immune system.

Most mutations are never processed, presented, or recognised by T cells so relying on prediction restricts the proportion of identified antigens that are therapeutically relevant.

Right Vectors

Strong, durable T cell responses
from a single dose
Our proprietary viral vectors are deliberately designed to stimulate strong and lasting protection against cancer, inducing highly durable T cell responses from a single dose.
In preclinical models we have demonstrated that T cells induced by our vector are durable and have the desired characteristics that enable them to continue to attack tumours long after vaccination.
We have shown that the generation of these T cells by our vector is associated with 80% survival in preclinical models.
Using a vector that is clinically de-risked, scalable and manufacturable with validated tumour-specific targets produces off-the-shelf precision vaccines that are deployable in specialist and community settings to serve broad populations of cancer patients.
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