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

Completed · Phase 2 · Has a placebo group

Conditions studied: Acute Kidney Injury

In brief

This study will evaluate the safety and efficacy of ABT-719 in preventing acute kidney injury in patients undergoing high risk cardiac surgery.

Key facts

Study ID

NCT01777165

Run by

AbbVie

People needed

240

Starts

2013-02-01

Expected to finish

2014-03-01

Last updated by the study team

2021-07-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject must be male or female, age greater than or equal to 18 years old.
• Subjects must have stable renal function, per Investigator discretion and no known increase in serum creatinine of greater than or equal to 0.3 mg during the preceding 4 weeks.
• Subjects with estimated glomerular filtration rate less than or equal to 60 mL/min/1.73 m2 who require intravascular iodinated contrast within 48 hours of the day of surgery, will only be included if there is no known serum creatinine increase greater than or equal to 0.3 mg.
• Subjects must be undergoing a pre-defined on-pump cardiac surgery meeting one of the following acute kidney injury risk factors:
• Subject is undergoing combined coronary artery bypass grafting (CABG) surgery and surgery of one or more cardiac valve (valve(s) surgery), or
• Subject is undergoing surgery of more than one cardiac valve (valves surgery), or
• Subject is undergoing surgery of the aortic root or ascending part of the aorta, or
• Subject is undergoing surgery of the aortic root or ascending part of the aorta, combined with coronary artery bypass graft and/or valve(s) surgery, or
• Subject has an estimated glomerular filtration rate greater than or equal to 16 mL/min/1.73 m2 and less than or equal to 59 mL/min/1.73 m2 as determined by Chronic Kidney Disease Epidemiology Collaboration (CKD EPI) formula at Screening, and is undergoing coronary artery bypass graft or single valve surgery.

You may not qualify if…

• Has an eGFR less than or equal to 15 mL/min/1.73 m2.
• Cardiac surgery to be performed without cardiopulmonary bypass.
• Has ongoing sepsis or history of sepsis within the last 2 weeks or untreated diagnosed infection prior to Screening visit. Sepsis is defined as presence of a confirmed pathogen, along with fever or hypothermia, and hypoperfusion or hypotension.
• Has known or documented RIFLE "R" or AKIN "Stage I" within the previous 4 weeks.
• Recently received (within the last 10 weeks) or is anticipated to receive chemotherapy which can interfere with kidney function

Where it is running

• Site Reference ID/Investigator# 83739 — Danbury, Connecticut, United States
• Site Reference ID/Investigator# 87720 — Gainesville, Florida, United States
• Site Reference ID/Investigator# 83746 — Jacksonville, Florida, United States
• Site Reference ID/Investigator# 83733 — Jacksonville, Florida, United States
• Site Reference ID/Investigator# 89178 — Tampa, Florida, United States
• Site Reference ID/Investigator# 87693 — Atlanta, Georgia, United States
• Site Reference ID/Investigator# 87717 — Augusta, Georgia, United States
• Site Reference ID/Investigator# 89180 — Fort Wayne, Indiana, United States
• Site Reference ID/Investigator# 101942 — Indianapolis, Indiana, United States
• Site Reference ID/Investigator# 85917 — Lexington, Kentucky, United States
• Site Reference ID/Investigator# 83732 — Bethesda, Maryland, United States
• Site Reference ID/Investigator# 83724 — Boston, Massachusetts, United States
• Site Reference ID/Investigator# 83745 — Boston, Massachusetts, United States
• Site Reference ID/Investigator# 83750 — Grand Blanc, Michigan, United States
• Site Reference ID/Investigator# 83747 — Petoskey, Michigan, United States
• Site Reference ID/Investigator# 83744 — Royal Oak, Michigan, United States
• Site Reference ID/Investigator# 85913 — Saint Paul, Minnesota, United States
• Site Reference ID/Investigator# 96455 — St Louis, Missouri, United States
• Site Reference ID/Investigator# 91253 — Omaha, Nebraska, United States
• Site Reference ID/Investigator# 93673 — Newark, New Jersey, United States
• Site Reference ID/Investigator# 83722 — New York, New York, United States
• Site Reference ID/Investigator# 89176 — Asheville, North Carolina, United States
• Site Reference ID/Investigator# 83723 — Durham, North Carolina, United States
• Site Reference ID/Investigator# 92413 — Gastonia, North Carolina, United States
• Site Reference ID/Investigator# 87733 — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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