ProBioGen and Eucodis sign agreement to commercialize C-LiNK, a novel ADC technology
Novel enzymatic, 1-step site-specific protein conjugation technology for ADC production.
ProBioGen and Eucodis Bioscience have jointly announced the signature of an exclusive license agreement on C-LiNK (CTAT), an innovative, site-specific antibody drug conjugation (ADC) technology. Under the agreement ProBioGen gains exclusive rights to commercialize Eucodis’ enzymatic C-terminal linking technology, and to offer it, together with its antibody development services, royalty-free to ADC-developing parties.
ProBioGen’s CEO, Dr. Wieland Wolf, commented: “This agreement is an excellent match between Eucodis’ enzyme engineering expertise and ProBioGen’s therapeutic protein-optimizing technologies and we look much forward to position C-LiNK and our contract manufacturing services right in the middle of the hot ADC field.”
Dr Karl Hübler, CEO of Eucodis explained: “We see a huge potential for C-LiNK in biopharma, especially in ADC development, but our expertise is engineering enzymes. Therefore, by teaming up with ProBioGen, our ADC conjugation technology will certainly get a much wider and quicker access to the community of therapeutic protein developing companies and we are convinced that our agreement with ProBioGen will result in fruitful collaborations within the industry.”
ProBioGen’s Chief Scientific Officer, Dr Volker Sandig, added: “This innovative ADC technology, which efficiently attaches any payload enzymatically via a pure peptide linker — as short as two amino acids — blends perfectly into our portfolio of robust cell line/product engineering technologies and manufacturing capabilities. The 1-step C-LiNK coupling technology will further open up the development space for ADCs and represents a competitive alternative to other Antibody-Drug Conjugate Technologies.”
Dr Jan Modregger, Eucodis’ Head of R&D stated: “Based on a trypsin variant engineered to enforce formation of a new peptide bond, our ADC conjugation technology links toxins or other molecules to the C-terminus of either antibody chain, without disturbing the native antibody structure. The outcome is a defined Drug-Antibody Ratio at high yield with low enzyme requirements and it offers on top the flexibility to add different payloads to separate sites in future ADCs.”
Related News
-
News Novartis signs US$3.2 bn subcutaneous delivery deal with Alteogen
Swiss pharma giant secures access to Korean biotech's ALT-B4 hyaluronidase platform in milestone-heavy agreement, marking Alteogen's fourth major licensing deal of 2026 as competition intensifies in the subcutaneous drug delivery space.
-
News Women in Pharma: The philosophy of pharmaceutical leadership
In this latest instalment of our Women in Pharma series, we sit down with Clarissa Sowemimo-Coker, Chief Strategy Officer at Ambrose Healthcare and CPHI Middle East Advisory Board Member.
-
News The PSCI Supplier Partnership - Collaboration for Responsible Supply Chains
About the Pharmaceutical Supply Chain Initiative The Pharmaceutical Supply Chain Initiative (PSCI) is the leading, member-led association for pharmaceutical companies working collaboratively to build responsible supply chains. Founded in 2006 and es... -
News AstraZeneca shares plunge 8.9% after reports of BMS talks
Britain's largest drugmaker lost more than GBP£17 billion in market value following reports of preliminary merger discussions with Bristol Myers Squibb that could create a pharmaceutical giant worth nearly US$400 billion, though investors rem... -
News GSK announces £400 million investment in new Cambridge R&D centre
Pharmaceutical giant to establish flagship research facility on Cambridge Biomedical Campus as part of strategic pipeline acceleration
-
News The CPHI Sustainability Summit - Where Conversation Becomes Collaboration
The Report Was Never the Destination - “The future of pharmaceutical sustainability won’t be shaped by individual organisations working in isolation. It will be shaped by partnerships, shared expertise and the willingness to work diffe... -
News Trump's generic drug tariffs set to reshape global pharmaceutical supply chains
The US president has announced plans to impose tariffs of up to 200% on imported generic medicines from August 2028, giving manufacturers a two-year window to establish domestic production facilities. The move threatens to upend a global supply chain t... -
News Building Safer, More Responsible Pharmaceutical Supply Chains: PSCI Global Audit Insights
The Pharmaceutical Supply Chain Initiative (PSCI) has released its seventh annual Audit Findings Analysis Report, offering unprecedented insights into supplier practices across the global pharmaceutical and healthcare industry.With a record-breaking 24...