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Terminated Phase 2 Interventional Results available

Safety & Efficacy of Eculizumab to Prevent AMR in Living Donor Kidney Transplant Recipients Requiring Desensitization

ClinicalTrials.gov ID: NCT01399593

Public ClinicalTrials.gov record NCT01399593. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 8:14 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-label, Multicenter Trial to Determine Safety and Efficacy of Eculizumab in the Prevention of Antibody Mediated Rejection (AMR) in Living Donor Kidney Transplant Recipients Requiring Desensitization Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this trial was to determine the safety and efficacy of eculizumab in the prevention of antibody-mediated rejection (AMR) in sensitized recipients of a living donor kidney transplant requiring desensitization therapy.

Study identification

NCT ID
NCT01399593
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alexion Pharmaceuticals, Inc.
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2, 2011 (Actual)
Primary completion
May 13, 2014 (Actual)
Completion
Nov 13, 2015 (Actual)
Last update posted
Oct 3, 2017

2011 – 2015

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294 —
Not listed La Jolla California 92037 —
Not listed Los Angeles California 90095 —
Not listed San Francisco California 94143 —
Not listed Washington D.C. District of Columbia 20007 —
Not listed Atlanta Georgia 30309 —
Not listed Chicago Illinois 60612 —
Not listed Baltimore Maryland 21205 —
Not listed Boston Massachusetts 02115 —
Not listed Rochester Minnesota 55905 —
Not listed St Louis Missouri 63110 —
Not listed Livingston New Jersey 07039 —
Not listed New York New York 10032 —
Not listed Chapel Hill North Carolina 27599 —
Not listed Cincinnati Ohio 45267 —
Not listed Oklahoma City Oklahoma 73112 —
Not listed Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01399593, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 3, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01399593 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →