We collaborate with leading industry and academic partners worldwide to advance the clinical development of promising cancer therapeutics.
As a partner, you can access our expertise in the early phase clinical development of small molecules, antibodies, vaccines, drug conjugates and other therapeutic modalities.
Contact us to find out moreSupported by an expert network of investigators, we leverage our drug development capabilities, expertise and infrastructure to demonstrate clinical potential.
We are motivated by delivering patient benefit, focusing on innovative, first-in-class agents and science-driven first-in-human trials.
We work with our partners to design, set-up and deliver clinical trials via our UK-wide and European network of investigators and early phase clinical trial centres. We take responsibility for all trial sponsor activities, helping complete preclinical packages, delivering regulatory submissions, clinical study management and ongoing medical support.
Our partners retain their background IP and receive a licence to the clinical trial results and all collaboration IP.
Our flexible co-development partnership model operates on a shared risk-reward basis offering a cost effective way for partners to progress the development of cancer therapies. We aim to recover a portion of our costs during the partnership and receive a fair share of future revenues if the agent is successful.
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We offer sponsorship of promising agents arising from academic research through our Drug Development Project scheme. Although our clinical trials are conducted in the UK and Europe, our partners are based around the world.
If you are based outside of the UK and have a cutting-edge oncology therapeutic, contact us to find out more about how we can help you develop it. All potential projects from both industry partners and academics are confidentially evaluated by our New Agents Committee through the Drug Development Project scheme.
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At the Centre for Drug Development, we have a team of over 100 scientists and operational staff located across the UK. Our in-house expertise includes translational science, preclinical transition, biomarker strategy and bioanalysis, medical oncology, trial design, protocol generation and pharmacovigilance.
From clinical trial planning to patient-centred trial management apps, we’re consulting, collaborating and partnering with people affected by cancer.