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NCT06215586 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Cardurion Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
303
Enrollment target

NCT06215586: Completed Phase 2 study, sponsored by Cardurion Pharmaceuticals.

NCT06215586 is a Phase 2 study that has completed, run by Cardurion Pharmaceuticals. The registered enrollment target is 303 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (128% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06215586, a Phase 2 study, has completed, sponsored by Cardurion Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
303 participants
Enrollment target

Study 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

Primary Outcome

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

Interventions

  • DRUG Placebo
  • DRUG Tovinontrine (CRD-750

Trial Details

FieldValue
Enrollment Target 303 participants
Start Date 2024-02-13
Est. Completion 2025-09-02
Phase Phase 2
Cardurion Pharmaceuticals

9 total trials

What the finished NCT06215586 record still lists

NCT06215586 is an interventional study that assigns participants to a tested intervention. The registered 303 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (128% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT06215586 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06215586 about?

NCT06215586 is a clinical study titled "Safety & Effectiveness of Tovinontrine in Chronic Heart Failure With Preserved Ejection Fraction (Cycle-2-PEF)". 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

What is the current status of trial NCT06215586?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 303 participants. The study started on 2024-02-13. Estimated completion is 2025-09-02.

What interventions are being tested in trial NCT06215586?

The interventions under investigation include: Placebo (DRUG), Tovinontrine (CRD-750 (DRUG).

Who is sponsoring clinical trial NCT06215586?

This trial is sponsored by Cardurion Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06215586's enrollment target sits among peer trials

303 167th of 2000 higher than 1,834 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06215586, the US trial registry maintained by the National Library of Medicine. NCT06215586 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.