Working collaboratively to provide end-to-end support across the project life-cycle.
We’ll evaluate candidate structures, provide expert advice on synthetic viability, and complete the synthesis of early targets.
We design synthetic routes and evaluate their viability with longer term goals of efficient, sustainable and robust process in mind.
During process optimisation, we develop appropriate purging points through the use of techniques such as crystallisation.
We understand the importance of manufacturing material with an impurity profile suitable for IND enabling studies.
At our Reading site we offer full cGMP manufacturing to support phase 1 and phase 2 clinical trials.
Our service offerings
We offer a comprehensive custom synthesis service to take your project from discovery to clinical trial
Dextra provide innovative synthetic solutions to the synthesis of carbohydrates and other complex molecules, frequently reducing the number of synthetic steps required to access the target compound. We offer expertly managed projects undertaken by our highly qualified and experienced chemists. Our integrated approach to product and process development enables seamless progression to large scale and GMP batches where required.
Our core competencies include complex oligosaccharide chemistry, route design, process development, optimisation and scale-up, process validation, technology transfer and GMP manufacture for Phase 1 and Phase 2 clinical trials.
Our fully equipped analytical laboratories offer expert support with a comprehensive range of analytical techniques available. All activities are fully supported by a strong Quality Management System and Health & Safety Framework and we have successfully achieved ISO9001:2015 registration.