Transforming Tumor Data

Into Personalized Immunotherapy.

Phase I

Clinical Trial Approved

8 Weeks

Biopsy to Treatment

3-in-1

Synergistic Formulation

The science

Three immune components acting in synergy

ODI-2001 combines three specific immune players — personalized synthetic DNA, a viral component and an immune checkpoint blocking antibody — formulated to induce and amplify a targeted immune response against what makes each tumor biologically unique.

01

Personalized synthetic DNA vector

A synthetic DNA expression system coding for the patient’s most immunogenic tumor neoantigens, identified through AI-driven genomic analysis.

02

MVA Viral Component

An attenuated virus that safely facilitates DNA expression and powerfully stimulates the innate immune system, amplifying the adaptive immune response.

03

Anti-CTLA4 antibody

An immunomodulating antibody that leverages the earliest steps of immune activation, removing inhibitory signals and sustaining the response.

Artificial intelligence makes true personalization possible.

The synthetic DNA advantage.

Safety

No bacterial contaminants

Cell-free production eliminates endotoxin risk entirely.

Safety

No antibiotic resistance genes

A cleaner regulatory and safety profile for every batch.

Speed

Fast, streamlined processes

Enabling a quick turnaround from biopsy to clinical preparation.

economics

Low cost of goods

A favorable economic profile supporting scalability across indications.