Boehringer Ingelheim has licensed Synaffix B.V.'s (a Lonza company) antibody-drug conjugate (ADC) technology, strengthening its oncology portfolio through its subsidiary, NBE Therapeutics. This collaboration aims to develop next-generation cancer treatments by combining Boehringer’s expertise with Synaffix’s clinically validated ADC platform.
ADCs are an innovative class of therapies that merge the precision of antibodies with the potency of cytotoxic drugs, ensuring targeted cancer cell destruction while minimizing harm to healthy tissue. Synaffix’s platform utilizes enzymatic glycan modification to enhance ADC efficacy, allowing for best-in-class ADC or bispecific development.
Peter van de Sande, Head of Synaffix, emphasized that Boehringer's adoption of their ADC technology validates its potential to optimize therapeutic outcomes. Lamine Mbow, Boehringer’s Global Head of Discovery Research, highlighted the company’s focus on developing a broad ADC pipeline targeting novel tumor spaces to improve cancer patient outcomes.
The agreement grants Boehringer access to Synaffix’s proprietary ADC technology for multiple targets, with the first target selected at signing. Additional targets will be nominated within a defined timeframe. The deal includes an upfront payment, potential milestone payments up to $1.3 billion, and royalties on net sales of resulting products.
Synaffix’s ADC platform, featuring GlycoConnect™, HydraSpace®, and toxSYN® technologies, enables rapid clinical development through an established supply chain and strong patent protection. Its business model revolves around target-specific technology out-licensing, as demonstrated by its growing partnered pipeline.
This partnership enhances Boehringer’s ability to address high unmet needs in oncology by advancing first-in-class ADC therapies, reinforcing its commitment to transforming cancer treatment.