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Interleukin (IL)-1 Blockade in Acute Heart Failure (Anakinra ADHF)

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Anakinra (high dose)
Anakinra (standard dose)
Placebo
Placebo
Sponsored by
Virginia Commonwealth University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure

Eligibility Criteria

21 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

All 5 criteria need to be met for enrollment of the patient in the study

  1. Primary diagnosis of acute decompensated heart failure within the last 24 hours as evidenced by both of the following:

    1. dyspnea or respiratory distress or tachypnea at rest or with minimal exertion
    2. evidence of elevated cardiac filling pressure or pulmonary congestion (at least one of the conditions must be met);

    i. pulmonary congestion/edema at physical exam OR chest x-ray; ii. plasma Brain Natriuretic Peptide (BNP) levels ≥200 pg/mL; iii.invasive measurement of left ventricular end-diastolic pressure >18 mmHg or of pulmonary artery occluding pressure (wedge) >16 mmHg.

  2. Left ventricular systolic dysfunction (LVEF<40%) during index hospitalization or prior 12 months.
  3. Age ≥18 years old
  4. Willing and able to provide written informed consent.
  5. Screening plasma C-reactive protein levels >5 mg/L.

Exclusion Criteria Subjects will not be eligible if they meet any of the following 15 exclusion criteria.

  1. The primary diagnosis for admission is NOT decompensated heart failure, including diagnosis of acute coronary syndromes, hypertensive urgency/emergency, tachy- or brady-arrhythmias.
  2. Concomitant clinically significant comorbidities that would interfere with the execution or interpretation of the study including but not limited to acute coronary syndromes, uncontrolled hypertension or orthostatic hypotension, tachy- or brady-arrhythmias, acute or chronic pulmonary disease or neuromuscular disorders affecting respiration.
  3. Recent (previous 3 months) or planned cardiac resynchronization therapy (CRT), coronary artery revascularization procedures, or heart valve surgeries.
  4. Previous or planned implantation of left ventricular assist devices or heart-transplant.
  5. Chronic use of intravenous inotropes.
  6. Recent (<14 days) use of immunosuppressive or anti-inflammatory drugs (not including Non-Steroidal Anti-Inflammatory Drugs [NSAIDs]).
  7. Chronic inflammatory disorder (including but not limited to rheumatoid arthritis, systemic lupus erythematosus).
  8. Active infection (of any type);
  9. Chronic/recurrent infectious disease (including Hepatitis B virus [HBV], Hepatitis C virus [HCV], and HIV/AIDS).
  10. Prior (within the past 10 years) or current malignancy.
  11. Any comorbidity limiting survival or ability to complete the study.
  12. End stage kidney disease requiring renal replacement therapy.
  13. Neutropenia (<2,000/mm3) or Thrombocytopenia (<50,000/mm3).
  14. Pregnancy.
  15. Angina, arrhythmias, or electrocardiograph (ECG) changes that limit maximum exertion during cardiopulmonary exercise testing obtained during the baseline testing.

Sites / Locations

  • Virginia Commonwealth University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Anakinra (short)

Placebo

Arm Description

Anakinra 100 mg twice daily for the first 3 days followed by 100 mg daily for days 4-14

Placebo injections twice daily for the first 3 days then once daily for days 4-14.

Outcomes

Primary Outcome Measures

C Reactive Protein
The proportional area-under-the-curve for plasma C reactive protein (CRP) levels measured during the first 3 days of admission. The proportion (y-axis) is calculated at each time-point with respect to the baseline CRP. The resultant y-axis is a unitless proportion. The x-axis is listed as "days"

Secondary Outcome Measures

Left Ventricular Ejection Fraction
Change in left ventricular ejection fraction (LVEF) between admission and 14 day follow up. This value is expressed as absolute change in measured LVEF. For example, if baseline LVEF = 20% and 14 day LVEF = 25%, this would be reported as an absolute change of 5%.
Brachial Artery Vasoreactivity
Change in flow mediated vasodilatation (FMD) of the brachial artery. Brachial artery FMD is calculated as the percentage increase in brachial artery diameter with hyperemia (an increase in the quantity of blood flow to a body part) induced relative to the resting brachial artery diameter. Percentage of brachial artery diameter is measured as FMD diameter/basal diameter. The change is FMD is reported as the % change in FMD from baseline to 14 days.

Full Information

First Posted
September 3, 2013
Last Updated
March 31, 2016
Sponsor
Virginia Commonwealth University
Collaborators
American Heart Association
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1. Study Identification

Unique Protocol Identification Number
NCT01936844
Brief Title
Interleukin (IL)-1 Blockade in Acute Heart Failure (Anakinra ADHF)
Official Title
Interleukin-1 Blockade in Acute Decompensated Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
May 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Virginia Commonwealth University
Collaborators
American Heart Association

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anakinra ADHF is a double-blind randomized clinical trial of anakinra, recombinant human interleukin-1 receptor blocker, or placebo in patients with acute decompensated heart failure with the aim to quench the acute inflammatory response, as measured by the area-under-the-curve for C reactive protein over 14 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Anakinra (short)
Arm Type
Experimental
Arm Description
Anakinra 100 mg twice daily for the first 3 days followed by 100 mg daily for days 4-14
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo injections twice daily for the first 3 days then once daily for days 4-14.
Intervention Type
Drug
Intervention Name(s)
Anakinra (high dose)
Intervention Description
Anakinra 100 mg daily twice daily for days 1, 2, and 3
Intervention Type
Drug
Intervention Name(s)
Anakinra (standard dose)
Intervention Description
Anakinra 100 mg daily for days 4-14
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo twice daily for days 1, 2, and 3
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo daily for days 4-14
Primary Outcome Measure Information:
Title
C Reactive Protein
Description
The proportional area-under-the-curve for plasma C reactive protein (CRP) levels measured during the first 3 days of admission. The proportion (y-axis) is calculated at each time-point with respect to the baseline CRP. The resultant y-axis is a unitless proportion. The x-axis is listed as "days"
Time Frame
3 days
Secondary Outcome Measure Information:
Title
Left Ventricular Ejection Fraction
Description
Change in left ventricular ejection fraction (LVEF) between admission and 14 day follow up. This value is expressed as absolute change in measured LVEF. For example, if baseline LVEF = 20% and 14 day LVEF = 25%, this would be reported as an absolute change of 5%.
Time Frame
14 days
Title
Brachial Artery Vasoreactivity
Description
Change in flow mediated vasodilatation (FMD) of the brachial artery. Brachial artery FMD is calculated as the percentage increase in brachial artery diameter with hyperemia (an increase in the quantity of blood flow to a body part) induced relative to the resting brachial artery diameter. Percentage of brachial artery diameter is measured as FMD diameter/basal diameter. The change is FMD is reported as the % change in FMD from baseline to 14 days.
Time Frame
14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All 5 criteria need to be met for enrollment of the patient in the study Primary diagnosis of acute decompensated heart failure within the last 24 hours as evidenced by both of the following: dyspnea or respiratory distress or tachypnea at rest or with minimal exertion evidence of elevated cardiac filling pressure or pulmonary congestion (at least one of the conditions must be met); i. pulmonary congestion/edema at physical exam OR chest x-ray; ii. plasma Brain Natriuretic Peptide (BNP) levels ≥200 pg/mL; iii.invasive measurement of left ventricular end-diastolic pressure >18 mmHg or of pulmonary artery occluding pressure (wedge) >16 mmHg. Left ventricular systolic dysfunction (LVEF<40%) during index hospitalization or prior 12 months. Age ≥18 years old Willing and able to provide written informed consent. Screening plasma C-reactive protein levels >5 mg/L. Exclusion Criteria Subjects will not be eligible if they meet any of the following 15 exclusion criteria. The primary diagnosis for admission is NOT decompensated heart failure, including diagnosis of acute coronary syndromes, hypertensive urgency/emergency, tachy- or brady-arrhythmias. Concomitant clinically significant comorbidities that would interfere with the execution or interpretation of the study including but not limited to acute coronary syndromes, uncontrolled hypertension or orthostatic hypotension, tachy- or brady-arrhythmias, acute or chronic pulmonary disease or neuromuscular disorders affecting respiration. Recent (previous 3 months) or planned cardiac resynchronization therapy (CRT), coronary artery revascularization procedures, or heart valve surgeries. Previous or planned implantation of left ventricular assist devices or heart-transplant. Chronic use of intravenous inotropes. Recent (<14 days) use of immunosuppressive or anti-inflammatory drugs (not including Non-Steroidal Anti-Inflammatory Drugs [NSAIDs]). Chronic inflammatory disorder (including but not limited to rheumatoid arthritis, systemic lupus erythematosus). Active infection (of any type); Chronic/recurrent infectious disease (including Hepatitis B virus [HBV], Hepatitis C virus [HCV], and HIV/AIDS). Prior (within the past 10 years) or current malignancy. Any comorbidity limiting survival or ability to complete the study. End stage kidney disease requiring renal replacement therapy. Neutropenia (<2,000/mm3) or Thrombocytopenia (<50,000/mm3). Pregnancy. Angina, arrhythmias, or electrocardiograph (ECG) changes that limit maximum exertion during cardiopulmonary exercise testing obtained during the baseline testing.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin W Van Tassell, PharmD
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data may be available upon request

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Interleukin (IL)-1 Blockade in Acute Heart Failure (Anakinra ADHF)

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