PHARMExcel was approached by global biotech, INmune Bio, to manage its UK/EU Phase I open label dose, escalation study of intravenous NK cell-targeted therapy in patients with high-risk Myelodysplastic Syndrome (MDS) and Acute Myelocytic Leukemia (AML).
We are a full-service Clinical Research Organisation (CRO) offering our Sponsors a unique ‘pick and mix’ service model – allowing INmune Bio to engage the specific services they needed tailored to the study requirements which included:
Despite the hurdles COVID-19 pandemic created, PHARMExcel worked closely with the regulators to obtain site approval quickly. The trial eligibility criteria also posed several challenges, but by working closely with the sites we minimized any risk of delaying the sites’ opening. Our expertise in complex ATMP regulatory processes ensured full regulatory compliance.
As a trial development partner PHARMExcel has the ability to adapt to biotech needs, providing expertise, ISO 9001 certified operational infrastructure and the relevant scalable services where needed.
"The most collaborative CRO I’ve worked with. PHARMExcel bothered to know us as a client and understands our studies inside out, making it an efficient and friendly partnership."
Prof Mark Lowdell, CSO INmune Bio Inc
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