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Clinical Trial ● Currently Recruiting Phase III NCT06830798

Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Ravulizumab Administered Intravenously in Adult Participants at High Risk of Delayed Graft Function After Kidney Transplantation

Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Ravulizumab Administered Intravenously in Adult Participants at High Risk of Delayed Graft Function After Kidney Transplantation…

📅 28 Apr 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT06830798
Start
2025-05-19
Completion
2028-02-04
ClinicaliQ Trial Snapshot
  • Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Ravulizumab Administered Intravenously in Adult Participants at High Risk of Delayed Graft Function After Kidney Transplantation — Recruiting • Phase III • NCT06830798.
  • Ravulizumab drug reduced need for dialysis after kidney transplant compared to placebo in high-risk patients.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

The primary objective of this study is to demonstrate the efficacy of ravulizumab vs placebo in reducing the severity of DGF as measured by time to freedom from dialysis in adult participants who are at high risk of DGF after undergoing transplant of deceased donor kidney. Conditions: Delayed Graft Function, DGF, Kidney Transplant Interventions: Ravulizumab, Placebo Lead Sponsor: Alexion Pharmaceuticals, Inc. Planned Enrollment: 450 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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