The Re-Prosper HF Study
Study Details
Study Description
Brief Summary
Heart failure with reduced ejection fraction (HFrEF) is a common cause for admission within the Veterans Affairs (VA) Health Care System.
It is associated with severe impairment of physical and mental health status and carries a high risk of mortality. Even though significant progress has been made in understanding the disease process, currently, its management and treatment is limited.
The investigators have discovered that a commonly used drug for the treatment of gout can be repurposed for the treatment of HFrEF.
The objective of this study is the treatment of outpatient Veterans with HFrEF with probenecid to improve heart and health function. Specifically, the investigators are testing whether oral probenecid administered orally twice per day for 180 days improves heart function as measured via ultrasound of the heart (aim 1); improves exercise capacity (aim 2); and improves self-report heart failure specific health status as measured via questionnaires (aim 3).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2/Phase 3 |
Detailed Description
Heart failure with reduced ejection fraction (HFrEF) is a common cause for admission within the Veterans Affairs (VA) Health Care System. It is associated with severe impairment of physical and mental health status and carries a high 5-yr mortality rate of ~75%. Even though significant progress has been made in understanding its pathophysiology, currently, its management and treatment is based on therapeutic targeting of a limited number of receptors and pathways.
The investigators' team and others have made great progress in the last few years by understanding and harnessing the Transient Potential Receptor superfamily as regulators of cardiovascular function. Specifically, the investigators' laboratory has explored the role the vanilloid 2 (TRPV2) subtype plays in regulating calcium handling and contractility. This work has led researchers to understand that TRPV2 modulates contractility via increasing calcium cycling in myocytes on a beat-to-beat basis.
The investigators have used probenecid, a generic, globally available drug with an extremely safe profile that has been used for decades as a treatment for gout, as a TRPV2 agonist. The investigators' work with this drug has demonstrated it to be a potent inotrope without apoptotic, chronotropic or arrhythmogenic effects in cardiomyocytes in vitro as well as in vivo murine and porcine models. These findings have been taken to the bedside with a recently published small phase 2 study of 20 adult patients with HFrEF (the ReProsper HF pilot study) where the investigators demonstrated a mean improvement in left ventricular systolic and diastolic function with no adverse effects after only 1 week of treatment. The use of probenecid in HFrEF was also indirectly supported by a recent retrospective study of approximately 40,000 patients in the Medicare database that found treatment with probenecid (not specifically for heart disease) was associated with a 9% decreased risk of HF hospitalization. These studies strongly argue for the safety and potential efficacy of probenecid to improve systolic function and the need for a larger study, and of longer duration that also evaluates functional and health status outcomes in addition to systolic function.
The overall objective of this study is the treatment of outpatient Veterans with NYHA II-III heart failure with reduced ejection fraction (HFrEF) with probenecid to improve systolic and health function. Specifically, the investigators are proposing a three-site double-blinded, randomized, placebo-controlled, trial that will assess whether oral probenecid administered at 1 gr. orally twice per day for 180 days in patients with NYHA II-III HFrEF improves systolic function as measured via ejection fraction with echocardiography (aim 1); improves functional status as measured by exercise stress testing (aim 2); and improves self-report heart failure specific health status as measured by Kansas City Cardiomyopathy Questionnaire (KCCQ) and overall health status measured by EQ5D (aim 3).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Probenecid 1 gr. orally of probenecid twice daily for 180 days |
Drug: probenecid
1 gr. orally of probenecid twice daily for 180 days
|
| Placebo Comparator: Placebo identical placebo (to probenecid tablets) for 180 days |
Drug: Placebo
identical tablets to probenecid
|
Outcome Measures
Primary Outcome Measures
- Change from baseline in cardiac function [6 months]
The main primary outcome is echocardiogram-derived EF. The investigators will use Definity echo contrast if adequate endocardial border definition cannot be ascertained for EF calculation in apical 4 and apical 2 using volumetric tracing analysis and modified Simpson's. The echosonographers from all sites will follow the same standard study ECHO procedure to obtain the views
Secondary Outcome Measures
- Change from baseline in exercise tolerance via a symptom-limited exercise test on a cycle ergometer [6 months]
The investigators will perform a maximal bicycle exercise stress test (BEST) on a cycle ergometer (Ergocard II, Esaote) with 25-W workload increments at 3-minute intervals. to adapt to patients with low functional capacity as previously described and with all the standard precautions. Results will be converted to Vo2 max using standard formula and compared to baseline
- Change from baseline in The Kansas City Cardiomyopathy Questionnaire (KCCQ) and EQ5D [6 months]
The Kansas City Cardiomyopathy Questionnaire (KCCQ) is a 23 item instrument validated in stable and decompensated HF patients with HFpEF and HFrEF. The questionnaire takes 4-6 minutes to complete and reflects disease-specific health status over the prior two weeks. Overall health status (EQ5D) (Appendix) is a well-known generic measure of health status. It has 5 questions that address five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety or depression) with five levels ranging from 'no problems' to 'extreme problems' each
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Have documented heart failure as a treated inpatient or outpatient diagnosis in the medical record.
-
Left ventricular ejection 40% within the past 12 months either by echocardiogram, cardiac MRI, cardiac CT, nuclear imaging or cardiac catheterization.
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History of admission to the hospital (or equivalent) for the treatment of acute decompensated heart failure (ADHF) within the past 1-12 months.
- Equivalent to hospitalization for ADHF
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Urgent care in the Emergency Department for ADHF
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Observation status for the treatment of ADHF
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Administration of intravenous diuretics in an outpatient setting
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IV inotrope use
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NYHA class II-III
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On stable GDMT for at least 2 weeks (including at least an EBM dose of betablocker and RAAS inhibition) consistent with the EPHESUS trial criteria [16] or having a documented allergy or adverse reaction to betablocker and/or RAAS inhibition.
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Age 18 years or older.
Exclusion Criteria:
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Acute coronary syndrome or cardiac revascularization within the past 3 months.
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End stage renal disease with renal replacement therapy or creatinine clearance less than 30 ml/min [17].
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Cardiac resynchronization therapy within the past 3 months.
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Constrictive pericarditis or restrictive cardiomyopathy on cardiac imaging study (echocardiogram cardiac MRI, cardiac CT) within the last 12 months.
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Ablation for cardiac arrhythmias within the past month.
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Peripartum cardiomyopathy diagnosed within past 6 months. If LVEF is still 40% after 6 months of diagnosis, they can be enrolled into the study.
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Admission to the hospital (or equivalent per above) for the treatment of HF within two weeks.
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Uncorrected cyanotic congenital heart disease.
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Greater than moderate degree of stenotic or regurgitant valvular disease.
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Terminal illness with expected survival of less than 12 months.
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Women who are pregnant, breast feeding, or plan to become pregnant during the study. All women in childbearing age will undergo baseline and quarterly urine pregnancy tests to ensure absence of pregnancy since the cardiometabolic assessments will be different during pregnancy.
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Oral therapy with probenecid for any indication during the preceding 3 months.
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Hypersensitivity to probenecid based on prior exposure.
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Inability to provide informed consent or study procedures due to dementia, unstable psychiatric disease, or other cause (e.g. inability to do perform exercise testing).
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Acute gout attack within the previous 3 months.
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Patients on the following medications: cephalosporins, quinolones, penicillins, methotrexate, zidovudine, ganciclovir, and acyclovir; since the excretion of these drugs is reduced due to probenecid [17]. If a patient is started on any of these medications the physician will be advised that it may increase their serum levels.
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History of uric acid kidney stones within the last year. Patient will be removed from the study if they develop urate kidney stones.
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History of blood diseases in the past year: Aplastic anemia, Hemolytic anemia, Leukopenia, Neutropenia, Pancytopenia, Thrombocytopenia or leukemia.
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Creatinine clearance (eGFR) <30 ml/min.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA | Boston | Massachusetts | United States | 02130 |
| 2 | Cincinnati VA Medical Center, Cincinnati, OH | Cincinnati | Ohio | United States | 45220 |
| 3 | Providence VA Medical Center, Providence, RI | Providence | Rhode Island | United States | 02908 |
Sponsors and Collaborators
- VA Office of Research and Development
Investigators
- Principal Investigator: Jack Rubinstein, MD, Cincinnati VA Medical Center, Cincinnati, OH
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CARA-006-19F
- I01CX001968