A humanised IgG1 monoclonal antibody targeting both the soluble and membrane-bound forms of the interleukin-6 receptor (IL-6R). By blocking IL-6 signalling at the receptor level, tocilizumab suppresses the acute-phase response, joint inflammation and systemic inflammatory cascades. Approved for RA, systemic and polyarticular JIA, giant cell arteritis and cytokine release syndrome. The SHIKARI® tocilizumab portfolio covers drug-level quantification, qualitative ADA screening and quantitative ADA titre measurement for complete TDM and immunogenicity research.

Tocilizumab has clinically important target biology, indication-specific dosing and measurable systemic exposure, making drug concentration and immunogenicity relevant research variables. Scientific source ↗ · EMA source ↗
Tocilizumab is a humanised IgG1 monoclonal antibody that binds both soluble and membrane-bound interleukin-6 receptor (IL-6R), inhibiting IL-6-mediated signalling. Source ↗
EMA-authorised uses include rheumatoid arthritis, systemic and polyarticular juvenile idiopathic arthritis, giant-cell arteritis, cytokine-release syndrome and selected severe COVID-19 settings under the approved product information. EMA source ↗
Published research provides study-specific concentration references for IL-6 receptor blockade and precision-dosing work:
Sandwich ELISA for the quantitative measurement of free tocilizumab drug concentration in serum and plasma. Calibrated against certified reference standards. 70-minute total assay time. Suitable for trough-level monitoring across IV and SC dosing regimens, pharmacokinetic profiling in RA and JIA populations, and dose optimisation research.
Bridging ELISA for the qualitative detection of anti-tocilizumab antibodies (ADA) in serum and plasma. Validated positive and negative cut-off controls included for definitive classification. 140-minute total assay time. Suitable for immunogenicity screening in RA, sJIA, pJIA and GCA cohorts, and as a first-line screen ahead of quantitative ADA titre confirmation.
Calibrated bridging ELISA for the quantitative determination of anti-tocilizumab ADA titre in serum and plasma. Confirmation reagent included for drug interference assessment. 140-minute total assay time. Suitable for longitudinal ADA titre monitoring, dose-response correlation and comparative immunogenicity research across biologic classes in rheumatology and paediatric populations.
| Kit Name | Catalog Code | Type | Analyte | ELISA Format | Tests | Storage |
|---|---|---|---|---|---|---|
| SHIKARI® Q-TOC | TOC-FD-ACT | Drug Levels Kit | Free tocilizumab concentration | Sandwich ELISA | 96 | 2–8°C |
| SHIKARI® S-ATOC (Qualitative) | TOC-QLS-ACT | Qualitative ADA Kit | Qualitative anti-tocilizumab ADA | Bridging ELISA | 96 | 2–8°C |
| SHIKARI® S-ATOC (Quantitative) | TOC-QNS-ACT | Quantitative ADA Kit | Anti-tocilizumab ADA titre | Bridging ELISA | 96 | 2–8°C |
Tocilizumab TDM differs from anti-TNF monitoring in that receptor saturation — not just drug exposure — is the pharmacodynamic endpoint. Selecting the right assay format is critical.
Our team can advise on kit selection, assay validation support, and research programme pricing. All SHIKARI® ELISA kits — developed by Matriks Biotek and distributed exclusively in the EU by Matrix Biotek — are available through our European headquarters in Barcelona, Spain.