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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 Jul 21, 2026, 10:14 PM 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

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

  • Eculizumab Drug

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 1, 2011
Primary completion
May 12, 2014
Completion
Nov 12, 2015
Last update posted
Oct 2, 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 2, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01399593 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →