PRIME-CKD

Personalized Drug Response: IMplementation and Evaluation in CKD

Abstract

Chronic Kidney Disease (CKD) is one of the major causes of death in high income countries and its prevalence is growing rapidly. New therapies for the treatment of CKD have shown clear efficacy at a population level. Yet, individual patients respond differently with many patients showing suboptimal efficacy. This indicates that a ‘one size fits all’ approach is no longer sustainable. Currently there are no validated pharmacodynamic biomarkers in CKD that aid in guiding optimal therapy for individual patients. Furthermore, there remains a large gap between biomarker research and actual implementation of biomarker based care in daily clinical practice. Thus, there is an urgent need to validate and translate biomarkers as tools for daily clinical practice. PRIME-CKD has a unique advantage to address this challenge as it builds on recently discovered pharmacodynamic biomarkers for CKD treatment, and has access to a vast amount of clinical data, bio-samples. PRIME CKD will: 1) Provide a breakthrough in the pharmacotherapy of CKD with the validation and implementation of pharmacodynamic biomarkers which will advance personalized medicine. 2) Scientifically validate innovative clinical trial elements, pipelines and qualification procedures that can be used by researchers, diagnostics industries and regulatory authorities. 3) Establish a Stakeholder Network to truly engage patients, clinicians and other stakeholders in implementation of personalized medicines 4) Develop a roadmap for biomarker use in daily clinical practice for the optimal treatment of CKD. These results will enable clinicians to match patients with CKD with the most effective available drug within the shortest possible timeframe leading to less disease burden and progression of disease, enhanced quality of life and increased cost-efficiency. PRIMECKD results will thus unlock the potential of biomarkers in healthcare and close the gap between biomarker research and clinical use in daily practice.

Project details

Unibo Team Leader: Gaetano La Manna

Unibo involved Department/s:
Dipartimento di Scienze Mediche e Chirurgiche

Coordinator:
Academisch Ziekenhuis Groningen(Netherlands)

Other Participants:
ALMA MATER STUDIORUM - Università di Bologna (Italy)

Third parties:
Irccs - Azienda Ospedaliero-Universitaria Di Bologna - Policlinico S.Orsola-Malpighi (Aosp) (Italy)

Total Eu Contribution: Euro (EUR) 9.696.831,00
Project Duration in months: 60
Start Date: 01/01/2023
End Date: 31/12/2027

Cordis webpage

This project has received funding from the European Union’s Horizon Europe research and innovation programme under grant agreement No 101095146 This project has received funding from the European Union’s Horizon Europe research and innovation programme under grant agreement No 101095146