Intended use:

For in vitro diagnostic use. The RIDASCREEN® VDZ Monitoring is an enzyme linked immunosorbent assay intended for the quantitative determination of vedolizumab (VDZ, Entyvio®, anti- integrin α4β7) in human serum and plasma.

Product information

Vedolizumab (VDZ, Entyvio®) is approved for the treatment of patients with moderate to severe Crohn’s disease and ulcerative colitis in whom conventional therapy or anti-TNFα therapies were ineffective or not tolerated. It is a gut-specific, humanized monoclonal antibody targeting the α4β7-integrin protein, which is involved in the migration of lymphocytes to the gut. Similar as to anti-TNFα drugs, measurement of vedolizumab drug concentrations supports a personalized dosing strategy in patients treated with vedolizumab.

The RIDASCREEN® VDZ Monitoring and our other TDM assays are vital to personalize treatment of patients with Crohn’s disease and ulcerative colitis and better achieve therapeutic targets.

Key features:

  • CE-marked versions of the ELISA tests of KU Leuven
  • Highly specific antibodies
  • Ready to use reagents
  • Validated for use on automated ELISA systems, e.g. the Dynex DSX®
Specifications
Art. No. G09045
Test format Microtiter plate with 96 wells (12 strips with 8 removable wells each)
Incubation time 1 h 40 min
Files
InstructionsGerman
English
French
Italian
Spanish
SDSg09045_english.zip (English)
g09045_german.zip (German)
g09045_french.zip (French)
g09045_italian.zip (Italian)
g09045_spanish.zip (Spanish)
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