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

Heart Failure With Preserved Ejection Fraction Clinical Trial

— HFpEF  

Official title:

Exploratory Phase 2A, Double-blind, Placebo-Controlled, Dose Escalation Study to Determine the Safety, Tolerability, PD, and PK of HU6 for the Treatment of Subjects With Obese Heart Failure With Preserved Ejection Fraction (HFpEF)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05284617
• Other study ID #: RIV-HU6-2201
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: October 30, 2022
• Est. completion date: June 30, 2024

Study information

• Verified date: January 2024
• Source: Rivus Pharmaceuticals, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 2A, randomized, parallel-group, placebo-controlled, double-blind, within subject dose escalation trial with 3 dose levels of HU6 and placebo. Subjects will be randomized (1:1) either to HU6 or placebo. Two dose levels will be administered in sequential order (150 mg daily followed by 300 mg daily), each for 20 days, to reach the third and highest dose of 450 mg daily if safety and tolerability are demonstrated at the lower 2 preceding doses. Administration of the 450 mg high dose will continue for a total of 94 days, with a safety follow-up visit within ~14 days of the last dose.

Description:

This is a Phase 2A, randomized, parallel-group, placebo-controlled, double-blind, within subject dose escalation trial with 3 dose levels of HU6 and placebo. Subjects will be randomized (1:1) either to HU6 or placebo. Two dose levels will be administered in sequential order (150 mg daily followed by 300 mg daily), each for 20 days, to reach the third and highest dose of 450 mg daily if safety and tolerability are demonstrated at the lower 2 preceding doses. Administration of the 450 mg high dose will continue for a total of 94 days, with a safety follow-up visit within ~14 days of the last dose. Subjects will be screened over a 40-day period to determine their eligibility based on specific history, physical, laboratory, and imaging evaluations as per the Schedule of Assessments. While a single screening clinical site visit is indicated, an additional visit may be necessary to complete the screening procedures due to scheduling issues. A number of these assessments will serve as the baseline prior to drug administration. A central laboratory will be used for all assessments, including MRI, DEXA, clinical blood/plasma measures, transthoracic echocardiography, and CPET.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 62
• Est. completion date: June 30, 2024
• Est. primary completion date: May 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

1. Adult male or female, =40 years of age.

2. 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.

3. Body mass index (BMI) =30 kg/m2;

4. Signs and symptoms of HF in the judgement of the Investigator, and meets the following disease severity criteria: a. 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):

1. Men: Either septal wall thickness (cm) either =1.1 or posterior wall thickness =1.1;

2. 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.

5. 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.

6. 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.

7. 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.

8. Ambulatory (not wheelchair- or scooter-dependent) and able to perform upright exercise testing including a 6 MWT.

9. 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:

1. If treated with a loop or thiazide diuretic, must be on stable regimen, which dose permits a flexible diuretic dosing schedule.

Exclusion Criteria:

1. Life expectancy <1 year due to non-cardiovascular reasons, in the judgement of the Investigator.

2. History of malignancy within 5 years (except non-high-grade skin cancers, carcinoma-in-situ, or low-grade prostate cancer).

3. Weight change (gain or loss) of =10 pounds either by self-reporting or documented weight loss within the past 90 days.

4. Bariatric surgery prior to screening or planned bariatric surgery during the course of the study.

5. Treatment with GLP-1 receptor antagonist begun within 1 year of screening.

6. Treatment with SGLT2 inhibitors begun within 6 months of screening.

7. Intolerance to MRI or with conditions contraindicated for MRI procedures including but

not limited to:

1. Having surgical clips/metallic implants/shrapnel/internal electric implants; or

2. 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

3. Claustrophobia: history of severe claustrophobia that would lead to inability to conduct MRI.

8. Current acute decompensated HF requiring intravenous (IV) diuretics or recent (<1 month before screening) hospitalization for HF.

9. Primary cardiomyopathy (e.g., constrictive, restrictive, infiltrative, toxic, hypertrophic [congenital], congenital, or any other primary cardiomyopathy, in the judgement of the Investigator.

10. Active myocarditis (COVID-induced or otherwise).

11. Active collagen vascular disease.

12. Current greater than moderate left- or right sided valve disease, in the opinion of the Investigator.

13. Planned cardiac surgery or catheter intervention during the time of trial participation.

14. Prior documented EF <40% within the last 3 years.

15. Tachycardia (>110 beats/minute) at screening.

16. 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.

17. Untreated, life-threatening dysrhythmia.

Related Conditions & MeSH terms

• Heart Failure
• Heart Failure With Preserved Ejection Fraction

Intervention

Drug:
• HU6
HU6 is being evaluated for its efficacy in improving cardiovascular function in obese subjects with HF with preserved ejection fraction (HFpEF).
• Placebo
Placebo

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland
United States	National Heart Institute	Beverly Hills	California
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	Medical University of South Carolina	Charleston	South Carolina
United States	Northwestern University	Chicago	Illinois
United States	The University of Chicago Medical Center	Chicago	Illinois
United States	The Lindner Center for Research and Education at The Christ Hospital	Cincinnati	Ohio
United States	University of Texas Southwestern	Dallas	Texas
United States	New Generation of Medical Research	Hialeah	Florida
United States	Saint Luke's Mid America Heart Institute	Kansas City	Missouri
United States	Weill Cornell Medicine	New York	New York
United States	Mayo Clinic	Rochester	Minnesota
United States	Lundquist Institute for Biomedical Innovation at Harbor UCLA Medical Center	Torrance	California
United States	Wake Forest	Winston-Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Rivus Pharmaceuticals, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate weight reduction while on HU6 treatment	Assess the rate and amount of body weight loss over the course of HU6 treatment	5 months