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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT06215586

Public ClinicalTrials.gov record NCT06215586. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 3, 2026, 6:26 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT06215586
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Industry
Enrollment
303 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 13, 2024 (Actual)
Primary completion
Sep 2, 2025 (Actual)
Completion
Sep 2, 2025 (Actual)
Last update posted
Sep 1, 2026

2024 – 2025

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Cardurion Investigative Site Birmingham Alabama 35233 —
Cardurion Investigative Site Little Rock Arkansas 72204 —
Cardurion Investigative Site Orange California 92868 —
Cardurion Investigative Site Torrance California 90502 —
Cardurion Investigative Site Van Nuys California 91405 —
Cardurion Investigative Site Jacksonville Florida 32216 —
Cardurion Investigative Site Miami Florida 33137 —
Cardurion Investigative Site Hazel Crest Illinois 60429 —
Cardurion Investigative Site Peoria Illinois 61636 —
Cardurion Investigative Site Alexandria Louisiana 71301 —
Cardurion Investigative Site Covington Louisiana 70433 —
Cardurion Investigative Site St Louis Missouri 63110 —
Cardurion Investigative Site Buffalo New York 14215 —
Cardurion Investigative Site New York New York 10019 —
Cardurion Investigative Site Cleveland Ohio 44195 —
Cardurion Investigative Site Oklahoma City Oklahoma 73135 —
Cardurion Investigative Site Portland Oregon 97225 —
Cardurion Investigative Site Rapid City South Dakota 57701 —
Cardurion Investigative Site Nashville Tennessee 37232-7601 —
Cardurion Investigative Site Dallas Texas 75246 —
Cardurion Investigative Site McKinney Texas 75069 —
Cardurion Investigative Site Burlington Vermont 05401 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06215586, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 1, 2026 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06215586 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →