PROTECT-2: A Study of the Selective A1 Adenosine Receptor Antagonist KW-3902 for Patients Hospitalized With Acute HF and Volume Overload to Assess Treatment Effect on Congestion and Renal Function

Overview

The study is being conducted to examine whether KW-3902IV will result in greater improvement in signs and symptoms of heart failure, with less treatment failure than standard therapy, when it is added to IV loop diuretics in subjects with acute heart failure syndrome and renal impairment.

Full Title of Study: “A Multicenter, Randomized, Double-blind, Placebo-controlled Study of the Effects of KW-3902 Injectable Emulsion on Heart Failure Signs and Symptoms and Renal Function in Subjects With Acute Heart Failure Syndrome and Renal Impairment Who Are Hospitalized for Volume Overload and Require Intravenous Diuretic Therapy”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
  • Study Primary Completion Date: July 2009

Detailed Description

Loop diuretics are generally first line therapy in patients hospitalized with acute heart failure syndrome (AHFS). Their use far exceeds that of vasoactive agents. Tubuloglomerular feedback (TGF) is the body's compensatory response to avoid excess fluid loss, and it is activated when elevated sodium concentrations in the distal tubule are detected. TGF is proposed as a contributing factor for the observed diuretic resistance that occurs in patients with heart failure. Higher doses of diuretics are required to overcome the decreased natriuresis and reduced RBF induced by TGF. Ultimately, this action creates a vicious cycle of worsening renal function and diminished diuretic effectiveness. The primary pharmacologic rationale for the use of KW-3902 in subjects with AHFS is its mechanism of action as an adenosine A1 receptor antagonist. TGF promotes release of adenosine, and adenosine binding to A1 receptors causes vasoconstriction of the afferent arteriole, decreased RBF, and enhanced sodium reabsorption by the proximal tubule. This action results in a decrease in GFR, diminished renal function, and sodium and water retention. Blocking adenosine A1 receptors via a selective adenosine receptor antagonist may limit sodium reabsorption by the proximal tubules without triggering TGF. It promotes vasodilation of the afferent arteriole of the glomerulus, and thus, this strategy offers the potential to overcome diuretic resistance or enhance diuretic responsiveness. It may also reduce the need for increasing diuretic doses that have been associated with worse outcomes. The objectives of this study are to evaluate the effect of KW-3902IV in addition to intravenous (IV) loop diuretics (such as furosemide) on heart failure signs and symptoms, renal function, and safety in subjects hospitalized with AHFS, volume overload, and renal impairment, and to estimate and compare within-trial medical resource utilization and direct medical costs between patients treated with KW-3902IV versus placebo.

Interventions

  • Drug: rolofylline
    • rolofylline 30 mg IV QD; 3 days
  • Drug: Comparator: Placebo (unspecified)
    • rolofylline Pbo 30 mg IV QD; 3 days

Arms, Groups and Cohorts

  • Placebo Comparator: 1
  • Experimental: 2

Clinical Trial Outcome Measures

Primary Measures

  • effect on heart failure signs and symptoms
    • Time Frame: 3 Days
  • effect on renal function
    • Time Frame: 3 Days

Secondary Measures

  • safety
    • Time Frame: 3 Days
  • within trial medical costs compared to placebo
    • Time Frame: 3 Days

Participating in This Clinical Trial

Inclusion Criteria

1. History of heart failure of at least 14 days duration for which diuretic therapy has been prescribed 2. Hospitalized for acute heart failure syndrome requiring IV diuretic therapy. 3. Impaired renal function Exclusion Criteria:

1. Acute contrast induced nephropathy 2. Ongoing or planned IV therapy for heart failure with positive inotropic agents, vasopressors, vasodilators, or mechanical support with the exception of IV nitrates 3. BNP <500 pg/mL or NT-pro-BNP <2000 pg/mL 4. Ongoing or planned treatment with ultrafiltration, hemofiltration, or dialysis 5. Severe pulmonary disease 6. Significant stenotic valvular disease 7. Heart transplant recipient or admitted for cardiac transplantation 8. Clinical evidence of acute coronary syndrome in the 2 weeks prior to screening 9. Heart failure due to significant arrhythmias 10. Acute myocarditis or hypertrophic obstructive, restrictive, or constrictive cardiomyopathy. 11. Known hepatic impairment 12. Non-cardiac pulmonary edema, including suspected sepsis 13. Allergy to soybean oil or eggs 14. History of seizure 15. Stroke within 2 years 16. History of or current brain tumor of any etiology 17. Brain surgery within 2 years 18. Encephalitis/meningitis within 2 years 19. History of penetrating head trauma 20. Closed head injury with loss of consciousness (LOC) over 30 minutes within 2 years 21. History of, or at risk for, alcohol withdrawal seizures 22. Advanced Alzheimer's disease 23. Advanced multiple sclerosis 24. Hgb <8 g/dL, Hct <25%, or the need for a blood transfusion 25. Previous exposure to KW-3902

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • NovaCardia, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
  • Collaborator
    • Merck Sharp & Dohme LLC
  • Provider of Information About this Clinical Study
    • Executive Vice President, Clinical and Quantitative Sciences, Merck & Co., Inc.
  • Overall Official(s)
    • Barry Massie, MD, Study Chair, University of California San Francisco, USA
    • Christopher O’Connor, MD, Study Chair, Duke University, USA
    • Marco Metra, MD, Principal Investigator, University of Brescia, Italy

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