Platforms

Three platforms, five programs, one approach.

Each platform is a different biological entry point into the same idea: use RNA to help the immune system recognize and attack solid tumors.

IONC101 / IONC102

Multilamellar RNA nanocomplex

Phase I ongoing in glioblastoma

IONC201 / IONC202

UNIFYR

Phase II/III planned

TAR001

Tumor-targeted nanoparticles

IND/CTA-ready; first-in-human planned

IONC101 / IONC102

Multilamellar RNA nanocomplex

Priming the battlefield and programming a precision tumor attack.

RNA is delivered in layered lipid particles to prime a broad immune response against tumor antigens. IONC101 is designed to prepare the patient’s immune system for battle: by selectively engaging systemic and intratumoral innate immune sensors, the platform creates an environment primed for a potent, targeted tumor attack.

Through its unique structure–function relationship, IONC101 delivers a personalized set of tumor-specific antigens while conditioning the patient’s immune landscape, so that newly reprogrammed immune cells have the signals and support they need to overcome tumor defenses and sustain a durable anti-cancer response.

IONC102 pairs the same delivery platform with AI-optimized, off-the-shelf antigens, starting in glioblastoma. Through a partnership with SandboxAQ, an Alphabet spinout, iOncologi is using AI to design and optimize the antigens for IONC102.

Diagram: the multilamellar RNA nanocomplex triggers a danger response and tumor antigen release, chemokines and cytokines recruit monocytes and naive T cells, and activated dendritic cells present antigen to drive local and systemic adaptive immunity.
How it works. The nanocomplex triggers innate immune activation and tumor antigen release, which drives antigen presentation and local and systemic adaptive immunity.

Clinical status

IONC101 is in Phase I clinical evaluation in adult and pediatric glioblastoma, with early translational data supporting activation of both innate and adaptive immune pathways and an acceptable safety profile.

IONC101

Personalized RNA nanocomplex

Glioblastoma, personalized

Phase I ongoing

IONC102

AI-optimized, off-the-shelf

Glioblastoma

IND-enabling

IONC201 / IONC202

UNIFYR

Off-the-shelf mRNA designed to prime the immune system to help more patients respond to checkpoint inhibitors.

UNIFYR is designed to be off the shelf. Because it does not depend on the tumor’s own sequence, no tumor biopsy or sequencing is needed to make it, and it is intended to apply across patients and across multiple solid tumor types.

The approach builds on iOncologi’s foundational U.S. patent, exclusively licensed from the University of Florida Research Foundation, covering RNA-based formulations that enhance tumor responsiveness to immune checkpoint inhibitors. Findings published in Nature Biomedical Engineering and Nature link RNA-driven immune activation to improved survival among cancer patients receiving immune checkpoint inhibitor therapy.

IONC201 UNIFYR

Off-the-shelf mRNA plus checkpoint inhibitor

NSCLC and other solid tumors

Phase II/III planned

IONC202 UNIFYR

Proprietary antigen mRNA plus checkpoint inhibitor

NSCLC

IND-enabling

TAR001 · TargImmune

Tumor-targeted nanoparticles

Tumor-targeting biodrones that kill tumor cells directly and activate the immune system.

TAR001 uses RNA nanoparticles targeted to EGFR-expressing tumor cells. It directly targets solid tumors with a novel payload designed to dismantle immune suppression within the tumor microenvironment.

Delivered through our proprietary tumor-targeted nanoparticle system, the platform is designed to reprogram local immune activity and sensitize tumors to immune checkpoint inhibitors. By restoring immune visibility and disrupting resistance pathways, it aims to turn “cold” tumors into inflamed, treatment-responsive sites and unlock the full potential of combination immunotherapies.

TAR001 is developed by TargImmune, an iOncologi subsidiary.

Diagram: a targeted nanoparticle binds tumor-specific receptors, enters the tumor cell and initiates multiple signaling cascades, leading to immunogenic cell death, pro-inflammatory cytokine secretion and recruitment of innate and adaptive immune cells.
How it works. Targeted nanoparticles bind tumor-specific receptors and trigger signaling cascades inside the tumor cell, leading to immunogenic cell death, cytokine release and immune cell recruitment.

Development status

TAR001 is IND/CTA-ready, with first-in-human studies planned in EGFR-positive solid tumors. Preclinical data show potent tumor-specific immune activation and synergy with checkpoint inhibitors.

TAR001

Tumor-targeted nanoparticles

EGFR-positive solid tumors

IND/CTA-ready; first-in-human planned

See where each program stands.

The pipeline shows all five programs across preclinical, IND-enabling and clinical stages.

Let’s talk about what comes next.

Whether you partner or collaborate in research, the team would like to hear from you.