drugset / Trial / NCT05049850

A Study to Investigate DSA Rebound in Patients Treated With Imlifidase Prior to Transplantation

NCT05049850

Phase 2 Terminated 3 enrolled Hansa Biopharma AB
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess whether imlifidase in combination with bortezomib, belatacept, rituximab and IVIg can suppress donor specific antibodies (DSA) and the occurrence of antibody-mediated rejection (AMR) in highly sensitized patients with chronic kidney disease with a positive crossmatch towards their living donor during a period of 3 months from transplantation.

Timeline

Start
2022-12-16
Primary completion
2024-02-05
Completion
2024-05-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Imlifidase Protein / enzyme biologic 0.25 mg/kg Intravenous

Indications

No indication recorded.