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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 Jul 22, 2026, 5:08 PM EDT

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

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

Interventions

  • Tovinontrine (CRD-750 Drug
  • Placebo Drug

Drug

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 12, 2024
Primary completion
Sep 1, 2025
Completion
Sep 1, 2025
Last update posted
Nov 16, 2025

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 Nov 16, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06215586 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →