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CAR-based Cell Therapies with Fully Human Platforms

The right binder, delivered to the right immune cell
Overview
Fully Human CARs
Functional Screening
In Vivo Delivery

Innovations and a Toolkit Built for Cell Therapies

Nona Biosciences overcomes key challenges in CAR-based therapeutic development through an integrated set of modular technologies. Leverage our fully human HCAb-based VH domains, functional CAR screening tools, and antibody-directed LNP delivery to streamline development across both ex vivo and in vivo applications. From binder discovery to construct optimization to targeted gene delivery, our platforms support the full range of CAR T, CAR NK, and CAR M development

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A Modular Platform for CAR-based Therapies
mRNA-LNP
mRNA-LNP
encoding
CAR
T Cell-Specific VH-Conjugated LNP
NonaCarFx™ Functional Screening

NonaCAR™: Fully Human HCAb-derived CAR

NonaCAR™ provides fully human VH domains derived from heavy chain-only antibodies (HCAbs) using our Harbour Mice® platform. These compact, stable domains are ideal for CAR-based cell therapies, supporting high surface expression, reduced immunogenicity, and flexible formatting for diverse construct designs. In addition to traditional ex vivo applications, NonaCAR™ domains also support next-generation delivery strategies such as in vivo programming through mRNA-based approaches.

Benefits of NonaCAR™:
  • Heavy Chain-Only Antibodies:
    Compact, single-domain VH antibodies reduce immunogenicity risks and avoid linker-related challenges seen in scFvs.
  • Fully Human Antibodies:
    Generated without the need for humanization, significantly lowering anti-drug antibody risks in HCAb-derived CAR therapies.
  • Simplified Structure:
    Optimized for efficient CAR design and flexible therapeutic applications.

NonaCarFx™:
Direct CAR-Function-Based Screening

Functional screening enables evaluation of binder performance directly in a cellular context for CAR-based therapy development. Nona’s platform supports selection based on activity rather than binding alone.

Explore Functional Screening

Reporter Cell-Based Lead VH Validation

To streamline CAR-based screening, Nona Biosciences has pioneered a cutting-edge dual-readout reporter cell line. This innovation enables efficient and dependable assessments of lead VH candidates, expediting your research endeavors.

In Vitro Assay Readouts

Nona Biosciences ensures robust performance of CAR-T therapies through detailed in vitro CAR-T cell characterization using human primary T cells. This evaluation is critical to confirming the functionality, safety, and efficacy of CAR-T products.

Key Evaluation Metrics:

Cytotoxicity:
Quantifies tumor-killing efficiency in target cells.

  

Cytokine Production:
Assesses immune modulation for optimal therapeutic impact.

  

Proliferation and Phenotype Analysis:
Confirms functional and durable CAR-T performance

In Vivo Cell Therapy, Enabled by Precision Targeting

Nona Biosciences supports in vivo CAR development through a modular platform that combines fully human antibody discovery, functional CAR screening, and targeted mRNA delivery. Using HCAb-derived VH domains identified through our Harbour Mice® platform, we screen CAR constructs for performance using NonaCarFx™ and apply site-specific conjugation to enable cell-directed lipid nanoparticle (LNP) delivery. This approach enables the direct programming of T cells in vivo, all without the need for ex vivo manipulation or preconditioning. Furthermore, our system has demonstrated efficient CAR expression and cytotoxic activity in primary T cell models, reinforcing its potential to streamline and scale next-generation cell therapy development.

CD8+ T Cell-Specific Delivery of CAR mRNA

Partnering with Umoja Biopharma on In Vivo CAR-T

Learn more about Umoja Biopharma

Nona Biosciences has teamed up with Umoja Biopharma to advance in vivo CAR-T therapies. By combining Nona’s HCAb Harbour Mice® and NonaCarFx™ platforms with Umoja’s VivoVec™ delivery system, the partnership aims to generate off-the-shelf CAR-T candidates with improved targeting and reduced immunogenicity.

Read the full press release

Ready to deliver the right CAR to the right cell?

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Explore Related Resources

LNP-mRNA Delivery Platform
CAR-T Characterization
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