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Improving Deceased-Donor Kidney Transplant Outcomes Via a Single Intragraft Injection of C1 Esterase Inhibitor (IMPROVE TRIAL)

Recruiting · Phase 2 · NCT06919003

Conditions: Kidney Transplant

At a glance

Research payments reported, 2025
$213,581
U.S. investigators named
2
Sites paid
1
Planned or actual enrollment
180

About the trial

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Tested
Berinert (biological), Placebo for Berinert (other)
Dates
Started 2025-09-22; completion 2032-05-30
Results posted
Not yet

The purpose of this study is to find out if Berinert can improve kidney function in the first year after transplant and to find out what effects, good or bad, Berinert will have in the kidney recipient. This research study will compare Berinert to placebo. The placebo looks exactly like Berinert but does not contain any active drug. Placebos are used in research studies to see if the results are due to the study drug or due to other reasons. Neither you or the study doctor can choose or know which group is assigned. The primary objective is to test whether intrarenal artery C1 esterase inhibitor (C1INH) injection into the donor kidney prior to transplantation improves kidney function in r…

From ClinicalTrials.gov, last updated 2026-02-27. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Csl Behring reported $213,581 in research payments for this study in 2025 (1 payments).

Products named: Berinert

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.