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Terminated Phase 2 Interventional Results available

Effectiveness of CRD-740 in Heart Failure

ClinicalTrials.gov ID: NCT05409183

Public ClinicalTrials.gov record NCT05409183. 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 Oct 24, 2026, 11:26 AM 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 Effectiveness of CRD-740 in Subjects With Chronic Heart Failure (CARDINAL-HF)

Brief summary

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

This is a study evaluating the effectiveness of CRD-740 in patients with either Heart Failure with Reduced Ejection Fraction (HFrEF) or Heart Failure with Preserved Ejection Fraction (HFpEF) after 12 weeks of treatment. The primary objective in Part A is to assess the effect of CRD-740 compared to placebo in plasma cGMP at Week 4 in HFrEF. Part B of the study was not conducted in favor of redesigned new studies.

Study identification

NCT ID
NCT05409183
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Industry
Enrollment
60 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
May 26, 2022 (Actual)
Primary completion
May 2, 2023 (Actual)
Completion
Jul 25, 2023 (Actual)
Last update posted
Dec 19, 2024

2022 – 2023

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Cardurion Investigative Site Alexander City Alabama 35010 —
Cardurion Investigative Site Birmingham Alabama 35211 —
Cardurion Investigative Site Fairhope Alabama 36532 —
Cardurion Investigative Site Torrance California 90502 —
Cardurion Investigative Site Hialeah Florida 33016 —
Cardurion Investigative Site Miami Florida 33133 —
Cardurion Investigative Site Miami Florida 33169 —
Cardurion Investigative Site Naples Florida 34102 —
Cardurion Investigative Site Tampa Florida 33612 —
Cardurion Investigative Site Atlanta Georgia 30303 —
Cardurion Investigative Site Hazel Crest Illinois 60429 —
Cardurion Investigative Site Alexandria Louisiana 71301 —
Cardurion Investigative Site Minneapolis Minnesota 55415 —
Cardurion Investigative Site Greensboro North Carolina 27408 —
Cardurion Investigative Site Tullahoma Tennessee 37388 —
Cardurion Investigative Site Allen Texas 75013 —
Cardurion Investigative Site Norfolk Virginia 23504 —

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05409183, 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 Dec 19, 2024 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05409183 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →