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Phase 3 Completed N=30 Randomized Quadruple-blind Treatment

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

Source: ClinicalTrials.gov NCT01936844 ↗
Enrolled (actual)
30
Serious AEs
20.0%
Results posted
Mar 2016
Primary outcomePrimary: C Reactive Protein — 2.09; 2.93 days
◆ Published Evidence
No publication linked

No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
C Reactive Protein
2.09; 2.93
SECONDARY
Left Ventricular Ejection Fraction
10; 0
SECONDARY
Brachial Artery Vasoreactivity
41.7; -45.2

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 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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01936844). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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