Bioprocess Development
with ADC-Integrated DSP Platforms
Xcellon Biologics delivers Bioprocess Development services designed for biologics and ADCs. Unlike traditional CDMOs, we don’t stop at upstream optimization, our services integrate conjugation workflows with a platform downstream purification (DSP) process specifically tailored for ADCs. This ensures scalable processes with consistent quality and reproducibility, reducing risks during GMP transfer.
What’s at Stake in Bioprocessing
Conventional development strategies often fall short for ADC programs. Protein engineering and upstream processes may deliver high expression, but without optimized conjugation and purification, programs risk free payload carryover, aggregation, and variability.
Integrated services covering protein engineering, upstream optimization, flexible conjugation strategies, platform DSP purification, process characterization, and tech transfer readiness enable scalable, reproducible workflows designed for CMC success and smooth IND advancement.
What We Offer
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Protein Engineering and Antibody Development
Gene cloning, mutagenesis, ORF optimization, antibody format engineering, Antigen production, epitope binding, in-silico modeling, internalization assays -
Cell Line Generation
Stable pool generation, clone selection, banking, expression optimization -
Upstream process optimization
Media/feed strategy development, cell culture optimization, DoE-based bioreactor studies -
Platform DSP purification
Robust clearance of free payloads, impurities, and aggregates. Fully integrated into typical antibody purification workflow. -
Process characterization
Identification of critical parameters and risk factors for scale-up by DoE, process risk assessment -
Tech transfer readiness
Scalable protocols designed for smooth handoff into GMP.
Integrated ADC Purification Platform
- Fully integrated to traditional antibody purification workflow
- Scalable platform for seamless tech transfer and CMC development
- Compatible with latest single use technologies
- Demonstrated to meet all ADC drug substance release criteria
Our bioprocess workflows directly support ADC development services, ensuring conjugation methods translate into scalable processes. They also prepare the foundation for future GMP manufacturing capabilities, reducing risk during clinical supply. Insights from analytical and formulation development feed back into process design, ensuring stability and DAR consistency are monitored throughout.
Build ADC processes with reproducibility and scalability in mind
FAQs for Bioprocess development
We integrate conjugation strategies with a platform DSP designed for ADCs, ensuring robust clearance of free payloads, aggregates, and impurities while maintaining scalability.
Our DSP platform is fully integrated into standard antibody purification workflows, meaning ADC-specific purification steps slot directly into established downstream processes. This ensures efficiency, reproducibility, and smooth GMP tech transfer.
Our glycoengineering platform enables site-specific DAR control (2, 4, 6, or 8) with high reproducibility. For programs requiring flexibility, we also offer cysteine, lysine, enzymatic, and click chemistries , all supported by DSP platform for batch-to-batch consistency.