Overview

Study to Evaluate Effects of INL1 in Patients With Heart Failure and Reduced Ejection Fraction

Status:
Recruiting
Trial end date:
2022-01-01
Target enrollment:
0
Participant gender:
All
Summary
This is a multicenter, randomized, double-blind, placebo-controlled, dose-response trial in patients with chronic stable Heart Failure (HF) and reduced Left Ventricular Ejection Fraction (LVEF) to evaluate the efficacy and safety of three INL1 doses compared with placebo. Patients will be treated for approximately 12 weeks with one of three INL1 doses: 50 mg, 150 mg, 300 mg, or, placebo capsules, taken twice daily (BID).
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Innolife Co., Ltd.
Criteria
Inclusion Criteria:

- Clinical diagnosis of HF requiring chronic treatment of loop diuretics

- Left Ventricular Ejection Fraction (LVEF) ≤ 40% at screening by echocardiography

- N-Terminal-prohormone of Brain Natriuretic Peptide (NT-proBNP) ≥400 pg/mL at screening
for patients without atrial fibrillation or atrial flutter, or, NT-proBNP ≥ 1,200
pg/mL at screening for patients with atrial fibrillation or atrial flutter

- Treated for Heart Failure with stable, optimal pharmacological therapy

- Acceptable screening echocardiographic image quality

Exclusion Criteria:

- Female patients of childbearing potential

- Patients with a New York Heart Association (NYHA) Class I or IV

- Heart failure that is clearly caused by toxin / drug such as Adriamycin

- Significant medical conditions or recent history suggesting the patient's study
participation will potentially pose a major risk to patient's safety and well-being

- Need for routine scheduled outpatient IV infusions for Heart Failure or scheduled
ultrafiltration

- History of rhabdomyolysis or history of autoimmune diseases

- Severe renal disease

- Hepatic disease

- Pulmonary disease limiting exercise capacity

- Atrial fibrillation with rapid ventricular response

- Life expectancy of less than 6 months

- Type 1 diabetes mellitus or Type 2 diabetes mellitus with very poor glycemic control

- Patients with anemia