Immune tolerance
IM injection breaks immune tolerance to activate B cells & produce polyclonal antibodies
Clinically validated approach with broad application across diseases - including oncology and autoimmune disorders
Proprietary technology allows for rapid development of novel therapies with multiple advantages over mAbs
Modality & RoA reduces cost & treatment burden, supporting patient access and quality of life.
Our proprietary technology platform enables the design of novel fusion molecules that combine our patented synthetic carrier construct with multiple antigens targeting specific proteins of interest. This approach breaks immune tolerance, stimulating the production of polyclonal antibodies that transiently deplete overexpressed ligands and cytokines, restoring them to normal physiological levels.
IM injection breaks immune tolerance to activate B cells & produce polyclonal antibodies
Polyclonal antibodies target multiple circulating ligands or cytokines
Tumor and environment are inactivated through depletion of ligands as fuel source
A focused oncology portfolio built from one repeatable immunotherapy platform.
IN01 is the lead clinical-stage asset, supported by four programs in discovery.
BRAF V600E and wild-type · Trials 1 and 2
Phase Ib approved 2021CTA reactivation in progressRare EGFR mutations · EPICAL II: IN01 + osimertinib
Phase Ib plannedThe approach behind IN01 can be applied to further growth factors.
Identify a growth factor behind tumour growth or treatment escape.
IN01 targets EGFUse the CTB carrier to raise neutralising antibodies.
IN01 fusion proteinPair with an inhibitor to remove the ligand it cannot reach.
IN01 plus an EGFR-TKIApply the route to another pathway or multiple targets.
IN11 and beyondA shared carrier provides precedent while every new target retains program-specific validation.
A shared process architecture can accelerate development, while each construct receives product-specific CMC validation.
An endogenous polyclonal response from IM injections — no monoclonal bioprocessing and no infusions.
Depleting EGF spares tissues that rely on other ligands, avoiding the skin and GI toxicity of receptor blockade.
Low treatment burden and no competition with the backbone; IN01 enhanced every inhibitor class tested.
One or two targets in a single injection, with five programs developed from the same platform.
IN01 provides platform precedent; each new target completes its own GLP tox, CMC validation and regulatory filing.
Co-Founder & CEO InPeutics
Co-Founder & CSO InPeutics
CMC & Tech Ops
Clinical Trials
Advisor – IP
Advisor – Molecule Design
Advisor – NSCLC