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Updated: Nov 16, 2025

Genetic Encoding of a Non-Canonical Amino Acid for the Generation of Antibody-Drug Conjugates Through a Fast Bioorthogonal Reaction
Published on: September 14, 2018
What makes a good antibody-drug conjugate?
Martin De Cecco1, Daniel N Galbraith1, Lisa L McDermott2
1Product Characterization, MilliporeSigma, Glasgow, UK.
Antibody-drug conjugates (ADCs) are vital cancer therapies. Advances in antibody, linker, and payload design are improving clinical success and expanding ADC applications to new cancer indications.
Area of Science:
- Oncology
- Pharmacology
- Biotechnology
Background:
- Antibody-drug conjugates (ADCs) represent a significant advancement in cancer therapy, with a growing number of approved agents.
- The intricate structure of ADCs, comprising antibody, linker, and payload, offers numerous design considerations.
Purpose of the Study:
- To provide a comprehensive overview of recent developments in ADC structural components.
- To analyze current trends in ADC design within the clinical landscape.
- To offer expert insights into the future of ADC development and application.
Main Methods:
- Review of current clinical landscape and developmental trends in ADC technology.
- Analysis of advancements in antibody, linker, and payload components of ADCs.
- Synthesis of expert opinion on structure-function relationships and future prospects.
Main Results:
- Significant progress has been made in understanding ADC structure-function relationships.
- Improved design strategies are emerging, addressing historical setbacks and discontinuation rates.
- The therapeutic potential of ADCs is expanding to novel targets and indications.
Conclusions:
- A deep understanding of ADC structure-function is crucial for translating design advances into clinical success.
- Continued innovation in ADC components will drive broader applications in oncology.
- The future of ADCs involves targeting new indications with novel payloads and antibodies.
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