The Guidant Bio FHAB mechanism of action

Our modular FHAB construct utilizes a validated, uniquely configured, albumin-binding approach to deliver selected payloads directly to the tumor microenvironment for enhanced penetration, retention and local activation.

Technology founded by industry expertise

Guidant Bio combines deep expertise in immune biology with integrated capabilities in drug discovery and product development. Our Fully Human Albumin-Binding (FHAB) construct is the foundation of a modular, Navigated Delivery™ platform for biologic therapeutics. Human serum albumin, the most abundant protein in plasma, undergoes receptor-mediated recycling via the neonatal Fc receptor (FcRn) and preferentially accumulates in inflamed tissues, including tumors, through active transport processes.

Guidant Bio FHAB-based therapeutics are built on engineered protein constructs that attach at a uniquely chosen site on native albumin, preserving FcRn engagement and albumin trafficking pathways. As a result, these therapies leverage the endogenous albumin transport biology to achieve prolonged systemic half-life and concentrated retention in the tumor microenvironment. By coupling therapeutic payloads to albumin, the FHAB platform enhances tissue exposure at sites of disease and improves the overall therapeutic index through reduced off-target distribution and systemic toxicity.

A modular drug delivery platform

A modular drug delivery platform

Albumin Binding

By attaching therapeutics to our albumin-binding fragment, we enable the therapeutic to persist in the bloodstream and accumulate in the tumor microenvironment.

For example, with cytokines as the therapeutic payload, this accumulation affords a greater chance to generate an anti-cancer immune response to the tumor cells.


Albumin Binding

By attaching therapeutics to our albumin-binding fragment, we enable the therapeutic to persist in the bloodstream and accumulate in the tumor microenvironment.

For example, with cytokines as the therapeutic payload, this accumulation affords a greater chance to generate an anti-cancer immune response to the tumor cells.


Navigated Delivery TM

Immune Activation with Dual-Cytokines

Publications

SON-1010 (IL12-FHAB) Synergizes with Trabectedin in Advanced Soft-tissue Sarcoma

Apr 7, 2026

SON-1010 (IL12-FHAB) Synergizes with Trabectedin in Advanced Soft-tissue Sarcoma

Apr 7, 2026

Combination immunotherapy with an albumin-binding interleukin-12 fusion protein that extends cytokine half-life, targets the tumor microenvironment, and enhances therapeutic efficacy

Presented at the 2025 American Association for Cancer Research (AACR) IO Conference

Mar 2, 2025

Combination immunotherapy with an albumin-binding interleukin-12 fusion protein that extends cytokine half-life, targets the tumor microenvironment, and enhances therapeutic efficacy

Presented at the 2025 American Association for Cancer Research (AACR) IO Conference

Mar 2, 2025

SON-1010: an albumin-binding IL-12 fusion protein that improves cytokine half-life, targets tumors, and enhances therapeutic efficacy

Published in Frontiers in Immunology

Dec 13, 2024

SON-1010: an albumin-binding IL-12 fusion protein that improves cytokine half-life, targets tumors, and enhances therapeutic efficacy

Published in Frontiers in Immunology

Dec 13, 2024

Expansion of a Phase 1 Study of SON-1010 (IL12-FHAB) Adding Trabectedin in Soft Tissue Sarcoma: Trial in Progress

Presented at the European Society For Medical Oncology (ESMO) Congress 2025

Dec 1, 2024

Expansion of a Phase 1 Study of SON-1010 (IL12-FHAB) Adding Trabectedin in Soft Tissue Sarcoma: Trial in Progress

Presented at the European Society For Medical Oncology (ESMO) Congress 2025

Dec 1, 2024

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