Exploratory Ph 2A, Double-Blind, Placebo-Controlled Dose Escalation Study of Safety, Tolerability, PD, & PK of HU6 for Subjects With Obese HFpEF

Prior treatment

• Bariatric surgery prior to screening or planned bariatric surgery during the course of the study.
• Treatment with GLP-1 receptor antagonist begun within 1 year of screening.
• Treatment with SGLT2 inhibitors begun within 6 months of screening.
• Current acute decompensated HF requiring intravenous (IV) diuretics or recent (\<1 month before screening) hospitalization for HF.
• Prior documented EF \<40% within the last 3 years.

Other illness

• History of malignancy within 5 years (except non-high-grade skin cancers, carcinoma-in-situ, or low-grade prostate cancer).
• Intolerance to MRI or with conditions contraindicated for MRI procedures including but not limited to:
  • Having surgical clips/metallic implants/shrapnel/internal electric implants; or
  • Inability to fit into MRI scanner due to subject habitus or exceeding weight tolerance limit of the scanner (generally, 350 or 400 lbs, dependent on manufacturer); or
  • Claustrophobia: history of severe claustrophobia that would lead to inability to conduct MRI.
• Active myocarditis (COVID-induced or otherwise).
• Active collagen vascular disease.
• Current greater than moderate left- or right sided valve disease, in the opinion of the Investigator.
• Planned cardiac surgery or catheter intervention during the time of trial participation.
• Atrial fibrillation or atrial flutter with an uncontrolled heart rate response or with a resting heart rate greater than 110 bpm by ECG at screening. Subjects may rescreen after appropriate adjustment of medication to manage the atrial fibrillation. A maximum of 16 subjects with this condition can be enrolled in this study.

Other

• Life expectancy \<1 year due to non-cardiovascular reasons, in the judgement of the Investigator.
• Weight change (gain or loss) of ≥10 pounds either by self-reporting or documented weight loss within the past 90 days.
• Primary cardiomyopathy (e.g., constrictive, restrictive, infiltrative, toxic, hypertrophic \[congenital\], congenital, or any other primary cardiomyopathy, in the judgement of the Investigator.
• Tachycardia (\>110 beats/minute) at screening.
• Untreated, life-threatening dysrhythmia.

• Adult male or female, ≥40 years of age.
• Competent to understand the information given in the Institutional Review Board (IRB) or Independent Ethics Committee (IEC) approved Informed Consent Form (ICF) and must sign the form prior to the initiation of any study procedures.
• Body mass index (BMI) ≥30 kg/m2;
• Signs and symptoms of HF in the judgement of the Investigator, and meets the following disease severity criteria:
  • KCCQ OSS ≤80; b. NYHA Classification Class II-III; c. Baseline peak VO2 ≤18 mL/kg/min for females or ≤20 mL/kg/min for males; d. Respiratory exchange ratio (respiratory quotient) (RER \[RQ\]) at baseline of \>1.0; e. Left ventricular ejection fraction (EF) ≥50%; f. At least 1 of the following objective criteria for HF: i. Documented hospitalization with HF as primary cause within in last year, or if greater than the past year, then with addition of structural heart disease on echocardiography (increased left atrial volume size or left ventricular hypertrophy, with sex-specific cut-points as per Lang, 2015) as follows:
  • Left ventricular hypertrophy (LVH):
  • Men: Either septal wall thickness (cm) either ≥1.1 or posterior wall thickness ≥1.1;
  • Women: Either septal wall thickness (cm) either ≥ 1.0 or posterior wall thickness ≥1.0;
  • Left atrial dilation (LAD): AP dimension (cm): ≥4.0 in men; \>3.8 in women; ii. Pulmonary capillary wedge pressure (PCWP) at rest \>15 mmHg (or left ventricular end-diastolic pressure \[LVEDP\] ≥18 mmHg) or \>25 mmHg (or 2.0 mmHg/L/min) with exercise in the last year; iii. E/e' ratio ≥14 at septal annulus at rest on Doppler and tissue Doppler imaging in the last year; or iv. Currently elevated NT-proBNP defined as \>125 pg/mL without atrial fibrillation and \>350 pg/mL for subjects with chronic controlled atrial fibrillation.
• Participants should maintain their stable level of physical activity throughout the duration of the study and must agree to not enroll in an exercise training program during the study.
• Participants should maintain their stable diet and no plan to enter into a weight loss program prior to or during the course of the study.
• Euthyroid as assessed by a thyroid profile utilizing thyroid stimulating hormone (TSH) and free thyroxine (T4) testing at screening. Subjects with a stable history of thyroid disease and who have been on stable doses of thyroid medications for a minimum of 4 months can be enrolled.
• Ambulatory (not wheelchair- or scooter-dependent) and able to perform upright exercise testing including a 6 MWT.
• Stable doses of medications (defined as no new medication or change in existing dose of medication ≥50%) for 30 days prior to screening, with additional specific criteria for the diuretics:
  • If treated with a loop or thiazide diuretic, must be on stable regimen, which dose permits a flexible diuretic dosing schedule.