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Clinical Trial Active — Not Recruiting Phase III NCT05369975

Efficacy and Safety in Imlifidase Desensitized Kidney Tx Patients, Including Two Non-Comparative Reference Cohorts

Efficacy and Safety in Imlifidase Desensitized Kidney Tx Patients, Including Two Non-Comparative Reference Cohorts — Active Not Recruiting • Phase III • NCT05369975.

📅 22 Apr 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase III
NCT ID
NCT05369975
Start
2022-04-19
Completion
2026-04
ClinicaliQ Trial Snapshot
  • Efficacy and Safety in Imlifidase Desensitized Kidney Tx Patients, Including Two Non-Comparative Reference Cohorts — Active Not Recruiting • Phase III • NCT05369975.
  • Imlifidase allows highly sensitized kidney transplant patients with positive crossmatch to receive transplants safely, with good one-year graft survival.

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What This Trial Is Studying

An open-label post authorization efficacy and safety study evaluating graft failure-free survival at 1-year in highly sensitized end-stage renal disease (ESRD) patients with positive crossmatch (XM) against a deceased donor prior to desensitized with imlifidase and subsequent kidney transplantation. Two non-comparative reference cohorts are included to assess the impact of differences in post-transplantation management and outcome in less sensitized patients. Conditions: Kidney Transplantation in Highly Sensitized Patients Interventions: Imlifidase, Normal Transplantation Routine Lead Sponsor: Hansa Biopharma AB Planned Enrollment: 225 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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