The Effects of IL-1 Blockade on Inotrope Sensitivity in Patients With Heart Failure (AID-HEART)

Recruiting now · Phase 1

Conditions studied: Heart Failure

In brief

End-stage heart failure (HF) is a progressive illness with a mortality rate similar to most advanced cancers.Roughly 5% of patients with HF have end-stage disease that is refractory to medical therapy (stage D heart failure). When patients reach this point in their disease, the only treatments known to prolong life are cardiac transplantation or left ventricular assist devices. In patients who do not qualify for these options, or elect a palliative approach, inotropes are frequently used to improve hemodynamics through an increase in cardiac output and reduction in filling pressures. While inotropes provide profound symptomatic relief, these benefits are accompanied by significant risks of progressive adverse cardiac remodeling, arrhythmias, and sudden death. There is, therefore, an urgent need to develop strategies to reduce the dose or duration of inotrope use in the management of patients with stage D of HF.

Key facts

Study ID

NCT06062966

Run by

Virginia Commonwealth University

People needed

20

Starts

2024-02-05

Expected to finish

2026-08-01

Last updated by the study team

2026-07-10

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Primary diagnosis for the clinic visit is stage D heart failure being on chronic stable dose of inotrope therapy (dobutamine or milrinone for the previous 28 days)
• Prior documentation of impaired left ventricular systolic function (ejection fraction <50%) at most recent assessment by any imaging modality (within 12 months)
• Stable dose of inotrope treatment without a recent hospitalization within the previous month
• Age ≥21 years and willing/able to provide written informed consent
• The patient is willing and able to comply with the protocol (i.e. self administration of the treatment, and exercise protocol).
• Screening plasma C-reactive protein levels >2 mg/L

You may not qualify if…

• Concomitant clinically significant comorbidities 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 that would interfere with the execution, interpretation, or completion of the study
• Recent (previous 3 months) or planned resynchronization therapy (CRT), or valve surgeries
• Previous or planned implantation of left ventricular assist devices or heart transplant within the next 3 months
• Recent (<14 days) use of immunosuppressive or anti-inflammatory drugs (including oral corticosteroids at a dose of prednisone equivalent of 0.5 mg/kg/day but not including inhaled or low dose oral corticosteroids or non-steroidal anti-inflammatory drugs)
• Chronic inflammatory disorder (including but not limited to rheumatoid arthritis, systemic lupus erythematosus)
• Active infection (of any type), including chronic/recurrent infectious disease (including HBV, HCV, and HIV/AIDS) - but excluding HCV+ with undetectable plasma RNA
• Prior (within the past 5 years) or current malignancy on targeted treatment - excluding carcinoma in situ [any location] or localized non-melanoma skin cancer
• Stage V kidney disease or on renal-replacement therapy
• Neutropenia (<1,500/mm3 or <1,000/mm3 in African-American patients)
• Pregnancy or breastfeeding
• Angina, hypertension, arrhythmias, electrocardiograph (ECG) changes, or other non-cardiac limitations that limit 6MWD obtained during the baseline testing
• Hypersensitivity to anakinra or to E. coli derived products

Where it is running

• Virginia Commonwealth University — Richmond, Virginia, United States (enrolling)

Full record on ClinicalTrials.gov

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