Therapeutic efficacy
Evaluate small molecules, degraders, antibodies, and other candidate interventions against arthritis progression.
The documented CIA platform uses DBA/1 mice and type II collagen immunization for rheumatoid-arthritis pharmacology studies involving T- and B-cell biology.
Documented efficacy programs include small molecules, degraders, and antibody-based interventions with serial clinical, immune, and histopathology readouts.
CIA studies in DBA/1 mice can combine longitudinal arthritis scoring and paw-thickness measurements with serum immunoglobulins, inflammatory cytokines, immune-cell profiling, and joint histopathology.
Evaluate small molecules, degraders, antibodies, and other candidate interventions against arthritis progression.
Serial serum total IgG and anti-type II collagen IgG1 measurements can be incorporated into the study design.
Spleen FACS analysis can quantify T-cell, B-cell, myeloid, neutrophil, plasma-cell, and related immune populations.
Histopathology workflows can include HE, TRAP, and Safranin O/Fast Green staining for joint and bone changes.
Endpoints are finalized with the selected model, species or strain, treatment design, and partner laboratory before study placement.
Arthritis score, body weight, and hind-paw thickness across induction and efficacy phases.
Serum total IgG and anti-type II collagen IgG1 by ELISA.
Inflammatory cytokines and protocol-defined spleen immune-cell populations by flow cytometry.
HE, TRAP, Safranin O/Fast Green, and quantitative histology scoring where included.
The exact induction schedule, treatment window, reference arm, sampling plan, and pathology package are confirmed during technical review.
Share the compound, mechanism, development question, preferred model, and intended endpoints. We can review fit, feasibility, and the appropriate partner-laboratory route for a CIA study.Required fields are marked with an asterisk(*).