Our Programs

ImmVue programs are built on the IMPAKT™ platform, designed to precisely tune intracellular immune signaling

Unlike traditional immune therapies that push the immune system broadly, IMPAKT molecules act at critical intracellular control points, allowing immune activity to be shaped with greater precision

Programs Built on Intracellular Immune Control

One platform. Two lead programs.

IMPAKT enables both immune activation and immune suppression from the same discovery architecture

IMPAKT-197 (Agonist)

Designed to enhance anti-tumor immunity; initial focus in solid tumors; combination logic with checkpoint-based approaches

IMPAKT-396 (Antagonist)

Designed to inhibit tumor-driving signaling; initial focus in T-cell lymphomas with dysregulated ITK signaling
 

Therapeutic Pipeline

IMPAKT-197 

ITK Agonist

Phase 1

IND-Enabling

Pre-Clinical

Late Discovery

IMPAKT-396

ITK Antagonist

Phase 1

IND-Enabling

Pre-Clinical

Late Discovery

Therapeutic Pipeline

IMPAKT-197 | ITK Agonist

IND-

Enabling

Pre-

Clinical

Late

Discovery

IMPAKT-396 | ITK Antagonist

IND-

Enabling

Pre-

Clinical

Late

Discovery

Why Current Approaches Fall Short

Traditional immunotherapies share a common limitation

Current immunotherapies do not directly target the intracellular TCR signaling machinery that determines T-cell activation strength. As a result, therapies must rely on indirect mechanisms that introduce trade-offs between efficacy, safety, and scalability

IMPAKT

Mechanism | First proven small-molecule ITK agonism; allosteric tunable, bidirectional

Structure/Design | Machine learning-driven

Format | Small molecules

Delivery | IV / Oral

Safety | Selective modulation of antigen-specific T cells

Modulation | Tunable immune control

Mechanism | Inhibition only / binary on-off

Structure/Design | Conventional MedChem or Antibody engineering

Format | Antibodies / Cell Therapy / Small Molecules

Delivery | IV / Oral / Cell therapy

Safety | Broad immune modulation

Modulation | Single-direction

IMPAKT

Typical IO/Kinase or Legacy Biologics

Mechanism

First proven small-molecule ITK agonism; allosteric tunable, bidirectional

Inhibition only / binary on-off

Structure/Design

Machine learning-driven

Conventional MedChem or Antibody engineering

Format

Small molecules

Antibodies / Cell Therapy /
Small Molecules

Delivery

IV / Oral

IV / Oral / Cell therapy

Safety

Selective modulation of
antigen-specific T cells

Broad immune modulation

Modulation

Tunable immune control

Single-direction