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Terminated Phase 2 Interventional

A Study to Evaluate the Safety and Efficacy of AC607 for the Treatment of Kidney Injury in Cardiac Surgery Subjects

ClinicalTrials.gov ID: NCT01602328

Public ClinicalTrials.gov record NCT01602328. 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 23, 2026, 12:05 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, Multicenter, Double-Blind, Placebo-Controlled Study of AC607 for the Treatment of Acute Kidney Injury in Cardiac Surgery Subjects

Study identification

NCT ID
NCT01602328
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
AlloCure Inc.
Industry
Enrollment
156 participants

Conditions and interventions

Interventions

  • AC607 Biological
  • Vehicle Only Biological

Biological

Eligibility (public fields only)

Age range
21 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
May 31, 2012
Primary completion
May 31, 2014
Completion
Jul 31, 2014
Last update posted
Aug 5, 2014

2012 – 2014

United States locations

U.S. sites
21
U.S. states
19
U.S. cities
20
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
University of California, San Diego San Diego California 92103
Stanford Hospital and Clinics Stanford California 94305-2299
MedStar Washington Hospital Center Washington D.C. District of Columbia 20010
Northwestern University Chicago Illinois 60611
Maine Medical Center Portland Maine 04102
Johns Hopkins University Baltimore Maryland 21287
Brigham and Women's Hospital Boston Massachusetts 02115
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Henry Ford Hospital Detroit Michigan 48202
Mayo Clinic Rochester Minnesota 55905
Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey 08903
Columbia University Medical Center New York New York 10032
Duke University Medical Center Durham North Carolina 27710
Ohio State University Columbus Ohio 43210
Lankenau Medical Center Wynnewood Pennsylvania 19096
UTHealth, The University of Texas Health Science Center at Houston Houston Texas 77030
Fletcher Allen Health Care - Renal Services Burlington Vermont 05401
University of Virginia Health System Charlottesville Virginia 22908
University of Washington Medical Center Seattle Washington 98195
CAMC Clinical Trials Center Charleston West Virginia 25304

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01602328, 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 Aug 5, 2014 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01602328 live on ClinicalTrials.gov.

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