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Clinical Assessment for Rheumatologic Disease - Research and Advancement in Safety and Efficacy

Study acronym: CARe RAiSE
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Study First Submitted
666 trials monitored
See 25 trials at risk
591 trials monitored
See 24 trials at risk
and 3 more diseases
The CARe RAiSE project represents a pioneering translational initiative aimed at advancing precision medicine in the treatment of autoimmune rheumatic diseases. The primary objective is the development and implementation of an innovative cell-based ex vivo assay that enables individualized prediction of therapeutic response to disease-modifying antirheumatic drugs (DMARDs). By identifying the most effective treatment option for each patient, this approach seeks to enhance therapeutic efficacy, reduce time to clinical response, and minimize healthcare costs. Despite the availability of numerous DMARDs, clinical decision-making remains largely empirical due to considerable interindividual variability in treatment response. This frequently results in a prolonged trial-and-error process, placing a significant burden on patients and the healthcare system. CARe RAiSE aims to overcome this limitation by providing a functional diagnostic tool that can predict a patient's immunological response to specific DMARDs prior to treatment initiation. The assay is based on peripheral blood mononuclear cells (PBMCs) obtained from individual patients, enabling a physiologically relevant assessment of immune responsiveness to targeted therapies. Combining high-content imaging with homogeneous well-based cytokine and inflammasome activity assays, the platform allows for a detailed single-cell analysis of inflammatory pathways. These data are used to generate predictive signatures of treatment response, thereby facilitating a mechanistically informed and personalized therapeutic strategy. Through this approach, CARe RAiSE introduces a scientifically grounded, efficient, and patient-specific method for DMARD selection, with the potential to substantially improve patient outcomes and reduce the socioeconomic impact of autoimmune rheumatic diseases.
Trial Details
NCT Number NCT07150000
Lead Sponsor University of Bonn
Conditions
(from sponsor)
Rheumatic Diseases, Rheumatoid Arthritis (RA), Giant Cell Arteritis (GCA), Psoriatic Arthritis (PsA), Axial Spondylarthritis (axSpA), Polymyalgia Rheumatica (PMR), ANCA Associated Vasculitis (AAV), Connective Tissue Disease (CTD) +5 more
Related terms Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis, Arthritis, Gouty, Arthritis, Psoriatic, Arthritis, Rheumatoid, Connective Tissue Diseases, Giant Cell Arteritis, Myositis, Polymyalgia Rheumatica, Rheumatic Diseases, Scleroderma, Systemic
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov