Safety & Effectiveness of Tovinontrine in Chronic Heart Failure With Preserved Ejection Fraction (Cycle-2-PEF)

Phase
Recruitment status
Participants
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Start date
Number of sites

Summary
The purpose of this study is to evaluate the safety and effectiveness of tovinontrine compared to placebo to lower NT-proBNP in patients with chronic heart failure with preserved ejection fraction
Acronym
Short title
Safety & Effectiveness of Tovinontrine in Chronic Heart Failure With Preserved Ejection Fraction (Cycle-2-PEF)
Official title
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Assess the Safety and Effectiveness of Tovinontrine in Patients With Chronic Heart Failure With Preserved Ejection Fraction

Control arm
Registry reports results
Listing at source
Recruitment status
Phase
Study type
Interventional

Completion date
First posted
Registry last updated
Primary completion date
Start date

Actual participants
Participants
Participant count basis
Protocol amendments
Number of sites

Data monitoring committee
Registry sponsor category
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Source registry
ClinicalTrials.gov

Registry ID
ClinicalTrials.gov ID
Registry record
Open registry record

Allocation
Randomised
Model
Parallel groups
Purpose
Treatment
Masking
Quadruple masking
Masked roles
Participants, Care providers, Investigators, Outcome assessors
Sources for study design

  1. Change in biomarkers from Baseline to Week 12 - NT-proBNP

    Timeframe: Baseline to Week 12

    The percent change in plasma NT-proBNP from Baseline to Week 12.

  1. Change in biomarkers at week 12 by treatment group - cGMP

    Timeframe: Baseline to Week 12

    The percent change in urine and plasma cGMP from Baseline to Week 12.

  2. Change in biomarkers at week 12 by treatment group - BNP

    Timeframe: Baseline to Week 12

    The percent change in BNP from Baseline to Week 12.

  3. Change in the biomarker ratio at Week 12 - NT-proBNP

    Timeframe: Baseline to Week 12

    The percent change in the urine and plasma cGMP to NT-proBNP ratio at week 12.

  4. Change in the biomarker ratio at Week 12 - BNP

    Timeframe: Baseline to Week 12

    The percent change in the urine and plasma cGMP to BNP ratio from Baseline to Week 12.

  5. The change from baseline in the Kansas City Cardiomyopathy Questionnaire-23 (KCCQ-23)

    Timeframe: Baseline to Week 12

    Scaled 0 to 100 where lower scores represent worse health status than higher scores

  6. The change from baseline in the KCCQ-23-CSS

    Timeframe: Baseline to Week 12

    The proportion of patients with a ≥5, 10, and 20-point improvement in the KCCQ-23-CSS at Week 12

  7. New York Heart Association (NYHA) classification at Week 12

    Timeframe: Week 12

    The post-baseline NYHA classification at Week 12

  8. Treatment Emergent Adverse Events (TEAEs)

    Timeframe: Baseline to Week 12

    The number of participants with TEAEs including drug related AEs, serious AEs (SAEs), and AEs leading to study drug discontinuation.

Sources for outcomes

Sex
All
Age groups
Adults, Older adults
Minimum age
18 Years
Healthy volunteers
No

  • Is an adult male or female patient ≥ 18 years of age

  • Has evidence in the medical history supporting a diagnosis of clinical HF syndrome, NYHA functional class II to III, with the duration of at least 6 months prior to the time of Screening. The HF syndrome is defined by documentation of 1 or more of the following:

    • At least 1 of the typical symptoms due to HF such as dyspnea and/or fatigue limiting exercise capacity;
    • At least 1 of the typical signs of HF such as peripheral edema, elevated jugular venous pressure, pulmonary crackles; or
    • Hospitalization, emergency department visit, or outpatient visit for HF requiring intravenous (IV) or subcutaneous (SQ) diuresis within the past 12 months.
  • Has ejection fraction (EF) >40% and left atrial enlargement by transthoracic echocardiogram (TTE) performed and interpreted locally at the time of Screening;

  • Has NT-proBNP level ≥ 300 pg/mL at the time of Screening. Patients with atrial fibrillation or flutter at the time of Screening are required to have an NT proBNP level of ≥500 pg/mL at the time of Screening;

  • Is on stable optimized doses of guideline-directed HF therapy, per Investigator's clinical judgment, for a minimum of 4 weeks prior to the time of Screening and during the Screening Period, with no planned changes after randomization; Has had no addition of new guideline-directed HF therapy within the 3 months prior to the time of Screening or during the Screening Period;

  • Has documented EF ≥ 60% by TTE within 6 months of the time of Screening or during the Screening Period;
  • Has evidence of recent HF exacerbation defined by hospitalization or requirement for IV or SQ diuretics within 60 days of the time of Screening or during the Screening Period;
  • Has a requirement for routine, scheduled outpatient IV infusions for HF (ie, inotropes, vasodilators, or diuretics) or routinely scheduled ultrafiltration;
  • Has elective interventions (eg, percutaneous coronary intervention, device implantations, percutaneous structural heart disease interventions, cardiac and non-cardiac surgery) planned to occur during involvement in this study;
  • Has acute coronary syndrome, stroke, transient ischemic attack, cardiac, carotid or other major cardiovascular surgery, or carotid angioplasty within 60 days of the time of Screening or during the Screening Period;
  • Has had a prior or planned orthotopic heart transplantation;
  • Has presence of or plan for mechanical circulatory support;

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Sources for eligibility

  • Cardurion Investigative SiteBirmingham, United States
  • Cardurion Investigative SiteLittle Rock, United States
  • Cardurion Investigative SiteOrange, United States
  • Cardurion Investigative SiteTorrance, United States
  • Cardurion Investigative SiteVan Nuys, United States
  • Cardurion Investigative SiteJacksonville, United States
  • Cardurion Investigative SiteMiami, United States
  • Cardurion Investigative SiteHazel Crest, United States
  • Cardurion Investigative SitePeoria, United States
  • Cardurion Investigative SiteAlexandria, United States
  • Cardurion Investigative SiteCovington, United States
  • Cardurion Investigative SiteSt Louis, United States
  • Cardurion Investigative SiteBuffalo, United States
  • Cardurion Investigative SiteNew York, United States
  • Cardurion Investigative SiteCleveland, United States
  • Cardurion Investigative SiteOklahoma City, United States
  • Cardurion Investigative SitePortland, United States
  • Cardurion Investigative SiteRapid City, United States
  • Cardurion Investigative SiteNashville, United States
  • Cardurion Investigative SiteDallas, United States
  • Cardurion Investigative SiteMcKinney, United States
  • Cardurion Investigative SiteBurlington, United States
  • Cardurion Investigative SiteChermside, Australia
  • Cardurion Investigative SiteBruges, Belgium
  • Cardurion Investigative SiteSint-Niklaas, Belgium

And 59 more, listed on the interactive page.

Sources for sites

  • 2023
  • 2023-508737-13
Sources for references

Related records

Drugs (1)

Lead sponsors (1)

Conditions (2)

Targets (1)