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Clinical Trial Summary

The rationale for the current protocol is to collect data from extended follow up in subjects that have received a kidney transplant following imlifidase dosing to provide a better understanding regarding the long-term outcome for these subjects. Data of parameters such as patient and graft survival, comorbidity, treatment of graft rejection episodes and quality of life as well as anti-drug antibody levels will be collected. This prospective, observational follow up study of subjects who have received imlifidase prior to kidney transplantation will provide important data to future prescribers and patients of the potential long-term benefits of imlifidase mediated transplantation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Kidney Transplant Failure and Rejection

NCT number NCT03611621
Study type Observational
Source Hansa Biopharma AB
Contact
Status Completed
Phase
Start date June 27, 2018
Completion date February 14, 2023

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