Adalimumab Humira®
The first fully human anti-TNF-α monoclonal antibody and a widely studied biologic in TDM research. Pharmacokinetic variability, treatment-emergent anti-drug antibodies and indication-specific exposure–response evidence make adalimumab a strong model for integrated drug and immunogenicity analysis. Six SHIKARI® kits address complementary research questions for the originator and biosimilars.

Why Adalimumab is widely studied in TDM research
Adalimumab was first approved in the United States in 2002 and authorised in the European Union in 2003. Its pharmacokinetic variability, treatment-emergent immunogenicity and indication-dependent exposure–response relationships make it an important subject for therapeutic drug monitoring research. FDA source ↗ · EMA source ↗
Molecular Target & Structure
Adalimumab is a fully human IgG1κ monoclonal antibody with a molecular weight of approximately 148 kDa that binds soluble and transmembrane TNF-α. FDA prescribing information ↗
Approved Indications
EMA-listed uses include rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis (including ankylosing spondylitis and non-radiographic axial spondyloarthritis), Crohn’s disease, ulcerative colitis, plaque psoriasis, polyarticular juvenile idiopathic arthritis, enthesitis-related arthritis, hidradenitis suppurativa and non-infectious uveitis. EMA source ↗
Selected Trough-Level Ranges
Published concentration–response studies report indication- and outcome-specific ranges:
Research-associated ranges, not universal treatment cut-offs. Values vary by endpoint, timing, assay method and population. This page is for RUO product information and does not provide clinical guidance.
Six complementary research assays
Enzyme immunoassay for the quantitative determination of adalimumab in serum and plasma. Developed for measuring drug concentration across the Cmin–Cmax range in trough-level and pharmacokinetic research.
Anti-idiotype monoclonal antibody-based assay for the specific and quantitative determination of free adalimumab. Distinguishes the pharmacologically active free-drug fraction from drug bound in immune complexes.
Enzyme immunoassay for the qualitative determination of antibodies to adalimumab in human serum and plasma. Designed for immunogenicity screening in research cohorts.
Enzyme immunoassay with confirmation for the quantitative determination of antibodies to adalimumab in serum and plasma. Supports longitudinal ADA measurement and correlation with drug-level data in research studies.
Dual-format kit for parallel measurement of free (unbound) and total (free + drug-complexed) anti-adalimumab antibodies. Includes proprietary dissociation buffer to release ADA from immune complexes — essential for drug-tolerant sample analysis and free-to-total ADA profiling.
Target Capture Neutralising Antibodies immunoassay for the qualitative detection of free neutralising antibodies to adalimumab in human serum and plasma.
Kit Specifications at a Glance
| Kit Name | Catalog Code | Type | Analyte | ELISA Format | Tests | Storage |
|---|---|---|---|---|---|---|
| SHIKARI® Q-ADA | ADA-FD-HUM | Drug Levels | Adalimumab concentration | Ligand-binding assay | 96 | 2–8°C |
| SHIKARI® QS-ADA | ADA-SPEC-ADA | Levels Specific | Specific free adalimumab (anti-idiotype) | Sandwich ELISA | 96 | 2–8°C |
| SHIKARI® S-ATA (Qualitative) | ADA-QLS-HUM | Qualitative ADA | Qualitative anti-adalimumab ADA | Bridging ELISA | 96 | 2–8°C |
| SHIKARI® S-ATA (Quantitative) | ADA-QNS-HUM | Quantitative ADA | Anti-adalimumab ADA | Quantitative immunoassay with confirmation | 96 | 2–8°C |
| SHIKARI® S-ATA Total (Duo) | ADA-QNFT-HUM | Free / Total ADA | Free and total anti-adalimumab ADA | Sandwich assay + dissociation buffer | 96 | 2–8°C |
| SHIKARI® T-CAP NAb™ | ADA-TCAP-NAb-HUM | T-CAP NAb™ | Free neutralising antibodies to adalimumab | Target Capture NAb Assay | 96 | 2–8°C |
Which kit fits your research question?
Each analytical question in biologic TDM research maps to a distinct assay type.
Publications Using SHIKARI® Adalimumab Kits 41
All journal publications below are drawn from the Matrix Biotek Publications library and are shown newest first. Records are included when the publication database identifies the biological drug and SHIKARI® product use.
Ready to order, or need technical guidance?
Our team can support kit selection, technical-information requests and research-programme quotations. SHIKARI® ELISA kits are developed and manufactured by Matriks Biotek in Ankara, with European commercial and research support from Matrix Biotek in Barcelona.