Interleukin-1 Blockade In Recently Decompensated Heart Failure - 2

Inflammation Clinical Trial

— REDHART2  

Official title:

The Effects of Interleukin-1 Blockade On Exercise Capacity In Patients With Recently Decompensated Systolic Heart Failure

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03797001
• Other study ID #: REDHART2 HM20014686
• Status: Recruiting
• Phase: Phase 2
• Start date: January 4, 2019
• Est. completion date: June 30, 2024

Study information

• Verified date: January 2024
• Source: Virginia Commonwealth University
• Contact: Benjamin Van Tassell, PharmD
• Phone: 804-828-4583
• Email: bvantassell[@]vcu.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

REDHART2 is a randomized, double-blinded, placebo-controlled trial to determine the effects of Anakinra on peak aerobic exercise capacity measured with a cardiopulmonary test after 24 weeks in patients with recently decompensated systolic heart failure and increased systemic inflammation.

Description:

The REDHART2 (REcently Decompensated Heart failure Anakinra Response 2 Trial) study is a phase II clinical trial of anakinra or placebo to determine improvement in aerobic exercise capacity (by measuring maximal oxygen uptake (VO2)) in patients with recently decompensated systolic heart failure (HF). The recently completed pilot REDHART study showed anakinra treatment for 12 weeks led to a significant improvement in peak aerobic exercise capacity, whereas anakinra treatment for 2 weeks did not, and no significant changes were seen in placebo. The REDHART2 study is designed to expand and confirm the beneficial effect of sustained anakinra treatment (24 weeks) on peak VO2, and to explore the potential effect size on hospital readmissions for HF. The rationale of Interleukin-1 (IL-1) blockade with anakinra in heart failure stems from the evidence of a) reduced adverse cardiac remodeling and heart failure in animal models of acute myocardial infarction (AMI); b) reduced incidence of heart failure in patients with ST-segment elevation AMI; c) enhanced IL-1 activity in patients with heart failure, d) quenching of the acute inflammatory response in patients with acute decompensated heart failure, e) direct cardiodepressant effects of IL-1 in animal models, f) improved exercise capacity in pilot studies including patients with stable systolic heart failure, stable diastolic heart failure, and, recently decompensated systolic heart failure in the pilot REDHART study. Patients will be randomized 2:1 to active treatment, such that patients will be twice as likely to receive anakinra versus placebo.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 102
• Est. completion date: June 30, 2024
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

All 6 criteria need to be met for enrollment of the patient in the study

1. Primary diagnosis for hospitalization is decompensated heart failure established as

the finding at admission of both conditions listed below:

• 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):

• pulmonary congestion/edema at physical exam OR chest XRay;
• plasma BNP levels =200 pg/mL;
• invasive measurement of left ventricular end-diastolic pressure >18 mmHg or of pulmonary artery occluding pressure (wedge) >16 mmHg.

2. The patient has a prior documentation of impaired left ventricular systolic function (ejection fraction =40%) at most recent assessment by any imaging modality (within 12 months).

3. The patient is now clinically stable, euvolemic, and meets standard criteria for

hospital discharge as documented by all the 3 conditions listed below:

• absence of dyspnea or pulmonary congestion/distress at rest;
• absence of pitting edema in the lower extremities, or in any other region;
• stable hemodynamic parameters (blood pressure, heart rate).

4. The patient is of age =21 years old, and is willing and able to provide written informed consent.

5. The patient is willing and able to comply with the protocol (i.e., self-administration, or exercise test).

6. The patient has screening high sensitivity plasma C-reactive protein levels (hsCRP) >2 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 resynchronization therapy (CRT), or 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 (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).

7. Chronic inflammatory disorder (including but not limited to rheumatoid arthritis, systemic lupus erythematosus).

8. Active infection (of any type), including chronic/recurrent infectious disease (i.e. HBV, HCV, and HIV/AIDS) - but excluding HCV+ with undetectable plasma RNA.

9. Active malignancy - excluding carcinoma in situ [any location] or localized non-melanoma skin cancer.

10. Any comorbidity limiting survival or ability to complete the study.

11. Stage V kidney disease or on renal-replacement therapy.

12. Neutropenia (<1,500/mm3 or <1,000/mm3 in African-American patients).

13. Pregnancy.

14. Angina, hypertension, arrhythmias, electrocardiograph (ECG) changes, or other non-cardiac limitations (i.e., peak respiratory exchange ratio VCO2/VO2 [RER]<1.0, reflecting sub-maximal test) that limit maximum exertion during CPX obtained during the baseline testing.

15. Hypersensitivity to Kineret or to E. coli derived products. 16) Evidence of COVID19 within the last 60 days or recent (21 days) exposure to close personal contact.

Related Conditions & MeSH terms

• Heart Failure
• Heart Failure, Systolic
• Inflammation
• Systolic Murmurs

Intervention

Drug:
• Anakinra
100 mg subcutaneous injection, daily for 24 weeks
• Placebo
subcutaneous injection, daily for 24 weeks

Locations

Country	Name	City	State
United States	Virginia Commonwealth University	Richmond	Virginia

Sponsors (1)

Lead Sponsor	Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	changes in peak oxygen consumption (VO2)	changes in peak oxygen consumption (VO2) after 24 weeks of treatment	baseline - 24 weeks
Secondary	changes in peak VO2 at earlier endpoints	changes in peak VO2 at earlier endpoints (6 and 12 weeks)	baseline - 6 weeks and baseline - 12 weeks
Secondary	echocardiography assessments	evaluation of heart function by standard echocardiography assessments at 24 weeks	baseline - 24 weeks
Secondary	hemodynamic assessments	estimates of arterial elastance at 6, 12 and 24 weeks	baseline - 24 weeks
Secondary	Quality of Life Assessments	Duke Activity Status Index will be administered at 6, 12 and 24 weeks to provide patient perception of changes. Responses are yes or no, with yes responses corresponding to better clinical condition.	baseline - 24 weeks
Secondary	Biomarker - high sensitivity C-reactive protein (CRP)	The change in blood levels of CRP will be measured from baseline to 24 weeks.	baseline - 24 weeks
Secondary	Biomarker - N-terminal pro b-type Natriuretic Peptide (NT-proBNP)	The change in blood levels of NT-proBNP will be measured from baseline to 24 weeks.	baseline - 24 weeks
Secondary	Clinical Outcome - cardiac death	Instances of cardiac death during the study will be recorded	baseline - 24 weeks
Secondary	Clinical Outcome - hospitalization for heart failure	Instances of hospitalization for heart failure during the study will be recorded	baseline - 24 weeks