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Antibody Drug Conjugate (ADC) Services

Antibody Drug Conjugate (ADC) Services

High control ADCs for real-world therapeutic development

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2
Conjugation technologies
3 weeks
From antibody to ADC
>90%
DAR homogeneity
ADC challenge, from proof of concept to clinical-ready material

Two conjugation technologies to power every ADC challenge, from proof of concept to clinical-ready material

ProteoGenix offers an extensive portfolio of chemical and enzymatic conjugation solutions. We help you select the optimal strategy based on key criteria such as:

    • Antibody structure
    • Payload properties
    • Scale-up requirements
    • Regulatory constraints

Whether you’re validating a concept or preparing for clinical phases, our experts and versatile conjugation toolbox ensure the most suitable solution for your program.

ADC-properties (1) (1)

Convert any antibody format into a potent ADC

Our platform supports all antibody formats, from VHHs to IgGs, including Fabs, scFvs, and bispecific antibodies.

Conjugate your antibody

Case report 

 

Discover how controlled ADC conjugation delivered a high-quality Vc-MMAE antibody-drug conjugate to support ovarian cancer proof-of-concept studies.

Case Report: Helping an Australian University Advance Ovarian Cancer Proof-of-Concept Studies with a Characterized ADC.

Read the case report

Achieve controlled toxicity profiles for ADC

Achieve controlled toxicity profiles

Perfectly controlled Drug-to-Antibody Ratio (DAR)

Our chemical and enzymatic conjugation technologies are designed to deliver >90% DAR homogeneity at the ratio you specify.
This tight DAR control, and its distribution, is essential for reducing ADC toxicity and avoiding the site-barrier effect.

Broad selection of linkers and payloads

Choose from a wide panel of cleavable and non-cleavable linkers, with expert guidance to ensure:

  • High stability in circulation to prevent premature payload release
  • Fast and targeted payload release inside the tumor cells

We also offer an extensive selection of payloads to tailor the optimal DAR/linker/payload configuration for your therapeutic objective.

Get a complete ADC characterization package

We provide a full analytical suite, including: DAR, DAR distribution, drug location, % free drug, and all standard antibody QC measurements.

More reasons to choose ProteoGenix for your ADC development

  • A true end-to-end partner

    From antibody generation to conjugation, we support every step. This integrated approach lets us also fine-tune antibody affinity and kinetics, two critical factors that directly impact your ADC’s therapeutic success.

  • ISO 9001:2015 certified

    Our ISO 9001:2015 certification ensures controlled, standardized, and traceable processes across all stages of your project.

  • Expert scientific guidance

    Because ADC development requires deep expertise, you are supported by dedicated PhD account managers throughout the project.

  • DAR control without antibody engineering

    Our chemical conjugation process allows DAR control even without prior antibody engineering.

Tool 

 

Download our dynamic and interactive checklist to thoroughly assess your antibody’s readiness across general criteria and specialized formats.

Download now

ProteoGenix’s ADC development workflow – From your antibody to your ADC in 3 weeks

From your antibody to your ADC in 3 weeks (does not include the optional steps)

Antibody selection (optional)
  • Customer provides the antibody

or

Antibody optimization (optional)
Antibody conjugation
  • Selection of the optimal antibody/linker/payload combination
  • Chemical or enzymatic conjugation
ADC characterization
  • DAR
  • DAR distribution
  • Additional QC analyses

ProteoGenix in the scientific literature

Publications

Lindland, K., Malenge, M. M., & al. (2024). Antigen targeting and anti-tumor activity of a novel anti-CD146 ²¹²Pb internalizing alpha-radioimmunoconjugate against malignant peritoneal mesothelioma. Scientific Reports, 14, 25941.

See the publication

Publications

Rioja-Blanco, E., Banz, Y., Schlapbach, & al. (2025). ¹⁶¹Tb Radioimmunotherapy as a Treatment for CD30-Positive Lymphomas. Journal of Nuclear Medicine, 66(6), 909–915. 

See the publication

FAQ about our ADC development service

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