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Terminated Phase 2 Interventional

A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prevention of Acute Kidney Injury in Subjects Undergoing High Risk Surgery

ClinicalTrials.gov ID: NCT01897519

Public ClinicalTrials.gov record NCT01897519. 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 Jun 26, 2026, 6:08 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 Phase 2b, Randomized, Double-Blind, Placebo Controlled, Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prevention of Acute Kidney Injury in Subjects Undergoing High Risk Major Surgery

Study identification

NCT ID
NCT01897519
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
56 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • ABT-719 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
Apr 30, 2013
Primary completion
Apr 30, 2014
Completion
Apr 30, 2014
Last update posted
Jun 5, 2014

2013 – 2014

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Site Reference ID/Investigator# 96295 Gainesville Florida 32610
Site Reference ID/Investigator# 96778 Jacksonville Florida 32207
Site Reference ID/Investigator# 96301 Tampa Florida 33613
Site Reference ID/Investigator# 96302 Fort Wayne Indiana 46804
Site Reference ID/Investigator# 101961 Indianapolis Indiana 46237
Site Reference ID/Investigator# 103356 Boston Massachusetts 02115
Site Reference ID/Investigator# 96303 Boston Massachusetts 02135
Site Reference ID/Investigator# 96997 Grand Blanc Michigan 48439
Site Reference ID/Investigator# 97878 Petoskey Michigan 49770
Site Reference ID/Investigator# 99377 Royal Oak Michigan 48073
Site Reference ID/Investigator# 99317 West Orange New Jersey 07052
Site Reference ID/Investigator# 96996 New York New York 10032
Site Reference ID/Investigator# 96296 Durham North Carolina 27710
Site Reference ID/Investigator# 102020 Cleveland Ohio 44195
Site Reference ID/Investigator# 103355 Columbus Ohio 43210
Site Reference ID/Investigator# 97556 Pittsburgh Pennsylvania 15232
Site Reference ID/Investigator# 103316 Providence Rhode Island 02903
Site Reference ID/Investigator# 102019 Memphis Tennessee 38120
Site Reference ID/Investigator# 108255 Charlottesville Virginia 22908
Site Reference ID/Investigator# 96300 Milwaukee Wisconsin 53215

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01897519, 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 Jun 5, 2014 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01897519 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →