Antibody-drug conjugation technology uses monoclonal antibodies (mAbs) to deliver potent, highly active pharmaceutical ingredients (HPAPIs) to targeted cells. In conjugated form, HPAPIs exhibit selective cytotoxicity which help spare non-target cells from toxic effects, thereby improving the overall safety profile of the therapy for the patient.
The complex nature of an ADC requires expertise in small and large molecule development, manufacturing, formulation and testing.
Choosing an experienced partner with these skills and the required containment facilities will advance your ADC to market. Whether you are looking to build your process based on our tailored technology platforms or need a service provider—or maybe even both—we can collaborate with you.
Tackle your manufacturing challenges with our technological innovations
ADCs require advanced manufacturing suites and dedicated equipment to characterize the molecule and demonstrate its purity, homogeneity and stability. They also require an extended containment strategy to protect operators and the environment from any contamination. We offer a comprehensive portfolio of products to fit your ADC manufacturing needs.
Rely on our expertise to help you develop the right process, the right systems and the right solutions for your ADC.
The search for the “magic bullet” to selectively deliver a cytotoxic agent to the site of a cancerous cell has been the goal of clinical oncology for more than 100 years. We offer a comprehensive portfolio of products and services that can help you bring your magic bullet to market faster and more efficiently.
Our ADC Express™ pre-clinical conjugation services help accelerate production of development-grade ADC constructs with essential analytical characterization of key quality attributes.
The combination of our extensive bioconjugation expertise and proven platform technology will efficiently turn your antibody and/or linker and payload into an ADC, enable scaling and shorten your path to the clinic.
ADC Express™ features