Research news
Selvita has become the first contract research organisation (CRO) to adopt Medicines Discovery Catapult’s (MDC) patented Chemical Protein Stability Assay (CPSA), under a new licensing agreement that will enhance its screening capabilities for drug development clients.
The CPSA provides rapid, reliable insights into target engagement – a critical factor in determining how well a drug candidate binds to its intended protein target. This data helps researchers confirm mechanism of action early, streamline candidate selection, and reduce the risks associated with later-stage failure.
Designed by MDC to simplify and accelerate this key stage in drug discovery, the assay can be deployed across a range of campaign formats, from hit identification through to hit-to-lead workflows. Its single-plate setup reduces variability, increases throughput, and avoids the complexity of traditional multi-step protocols.
Unlike approaches that require purified proteins, the CPSA uses crude cell lysates to evaluate compound-protein interactions in a more biologically relevant environment. It can be adapted for multiple protein types and readout methods, making it a flexible tool for discovery teams working across diverse therapeutic areas.
Selvita will integrate the assay into its screening cascades, offering clients improved data quality for faster, evidence-led decision-making in early-stage drug programmes.
Dr Francesca Sadler, Chief Commercial Officer at MDC, commented: “Selvita is the first CRO to license our CPSA technology, and we’re thrilled to see it applied in high-throughput commercial settings. This assay offers real advantages for innovators working to unlock difficult targets or de-risk candidate selection. It’s a key step forward in our mission to remove technical barriers and accelerate the delivery of better medicines.”
Dr Paul Overton, Chief Commercial Officer at Selvita, added: “This agreement aligns perfectly with Selvita’s strategy of continually strengthening our discovery platform. The CPSA provides scalable, reliable target engagement data - just what our customers need to move their drug discovery projects forward with confidence.”
More information online
ILM Guide 2026/27