Functional Impact of GLP-1 for Heart Failure Treatment (FIGHT)

• Status: Completed
• Trial end date: 2015-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective is to test the hypothesis that, compared with placebo, therapy with Subcutaneous (SQ) GLP-1 agonist in the post-Acute Heart Failure Syndrome (AHFS) discharge period will be associated with greater clinical stability at six months as assessed by a composite clinical endpoint.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Duke University
• Collaborator: National Heart, Lung, and Blood Institute (NHLBI)
• Treatments: Liraglutide

Criteria

Inclusion Criteria:

1. Age ≥ 18 years

2. AHFS as defined by the presence of at least 1 symptom (dyspnea, orthopnea, or edema) AND 1 sign (rales on auscultation, peripheral edema, ascites, pulmonary vascular congestion on chest radiography)

3. AHFS is the primary cause of hospitalization

4. Prior clinical diagnosis of HF

5. Left Ventricular Ejection Fraction(LVEF) ≤ 40% during the preceding 3 months (if no echo within the preceding 3 months, an LVEF ≤ 30% during the preceding three years is acceptable)

6. On evidence-based medication for HF (including beta-blocker and ACE-inhibitor/ARB) or previously deemed intolerant

7. Use of at least 80 mg or furosemide total daily dose (or equivalent) prior to admission for AHFS (a lower dose of a loop diuretic combined with a thiazide will count as an "equivalent")

8. Willingness to provide informed consent

Exclusion Criteria:

1. AHFS due to acute myocarditis or acute Myocardial Infarction

2. Ongoing hemodynamically significant arrhythmias contributing to HF decompensation

3. Inotrope, intra-aortic balloon pump (IABP) or other mechanical circulatory support use at the time of consent. Prior use will not exclude a patient.

4. Current or planned left ventricular assist device therapy in next 180 days

5. United Network for Organ Sharing status 1A or 1B

6. B-type natriuretic peptide(BNP)< 250 or NT-proBNP<1,000 (Not required per protocol but if available and too low would be an exclusion; within 48 hours of consent)

7. Hemoglobin (Hgb) < 8.0 g/dl

8. Glomerular filtration rate(GFR) < 20 ml/min/1.73 m2 within 48 hours of consent

9. Systolic blood pressure < 80 mmHg at consent

10. Resting Heart Rate > 110 at consent

11. Acute coronary syndrome within 4 weeks as defined by electrocardiographic (ECG) changes and biomarkers of myocardial necrosis (e.g. troponin) in an appropriate clinical setting (chest discomfort or anginal equivalent)

12. Percutaneous Coronary Intervention, coronary artery bypass grafting or new biventricular pacing within past 4 weeks

13. Primary hypertrophic cardiomyopathy

14. Infiltrative cardiomyopathy

15. Constrictive pericarditis or tamponade

16. Complex congenital heart disease

17. Non-cardiac pulmonary edema

18. More than moderate aortic or mitral stenosis

19. Intrinsic (prolapse, rheumatic) valve disease with severe mitral, aortic or tricuspid regurgitation

20. Sepsis, active infection (excluding cystitis) or other comorbidity driving the HF decompensation

21. Acute or chronic severe liver disease as evidenced by any of the following:

encephalopathy, variceal bleeding, International Normalized Ration (INR) > 1.7 in the absence of anticoagulation treatment

22. Terminal illness (other than HF) with expected survival of less than 1 year

23. Previous adverse reaction to the study drug

24. Receipt of any investigational product in the previous 30 days.

25. Enrollment or planned enrollment in another randomized therapeutic clinical trial in next 6 months.

26. Inability to comply with planned study procedures

27. Pregnancy or breastfeeding mothers

28. Women of reproductive age not on adequate contraception

29. History of acute or chronic pancreatitis

30. History of symptomatic gastroparesis

31. Familial or personal history of medullary thyroid cancer or multiple endocrine neoplasia type-2 (MEN2)

32. Prior weight-loss surgery (i.e., Roux-en-Y gastric bypass) or other gastric surgery associated with increased endogenous GLP-1 production

33. Prior or ongoing treatment with GLP-1 receptor agonists

34. Ongoing treatment with dipeptidyl peptide-IV inhibitors (1 week washout required)

35. Ongoing treatment with thiazolidinedione

36. Oxygen-dependent chronic obstructive pulmonary disease

37. Diabetic patients with history of 2 or more severe hypoglycemia, Diabetic Ketoacidosis(DKA) or hyperglycemic, hyperosmotic nonketotic coma in the preceding 12 months.

38. Diagnosis of Type 1 Diabetes Mellitus

40. If diabetic, inadequate glycemic control with glucose level > 300 mg/dL within 24 hours of randomization