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NCT06658899 · ClinicalTrials.gov registry record · Phase 2

A Phase 2 Study of CRD-4730 in CPVT

A Phase 2 study of Catecholaminergic Polymorphic Ventricular Tachycardia, sponsored by Cardurion Pharmaceuticals.

Recruiting
Registry status
Phase 2
Development phase
12
Enrollment target
9
Study locations

NCT06658899 is a Phase 2 study of Catecholaminergic Polymorphic Ventricular Tachycardia that is actively recruiting participants, run by Cardurion Pharmaceuticals. The registered enrollment target is 12 participants. The trial reports 9 study locations across 9 states.

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The verdict

NCT06658899, a Phase 2 study of Catecholaminergic Polymorphic Ventricular Tachycardia, is actively recruiting participants, sponsored by Cardurion Pharmaceuticals.

RECRUITING
Registry status
Phase 2
Development phase
12 participants
Enrollment target
9
Study locations

Study Summary

This is a Phase 2, multicenter, double-blind, sponsor blinded, placebo-controlled, repeat-dose clinical study of CRD-4730 to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of CRD-4730 to participants with Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). Participants with CPVT will complete a 3-period, randomized 3-sequence study. Each participant will be randomized to one of the 3 sequences in which they will receive 2 different doses of CRD-4730 and 1 dose of matching placebo.

Interventions

  • DRUG Placebo
  • DRUG CRD-4730

Study Locations (9)

California

  • Cardurion Investigative Site - San Francisco

North Carolina

  • Cardurion Investigative Site - Morrisville

Texas

  • Cardurion Investigative Site - Houston

Wisconsin

  • Cardurion Investigative Site - Madison

British Columbia

  • Cardurion Investigative Site - Vancouver

Other

  • Cardurion Investigative Site - Saint-Herblain

Pavia

  • Cardurion Investigative Site - Pavia

North Holland

  • Cardurion Investigative Site - Amsterdam

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2025-12-01
Est. Completion 2027-04
Phase Phase 2

Sponsor

Cardurion Pharmaceuticals

9 total trials

What the Registry Record Tells You About NCT06658899

The ClinicalTrials.gov registry entry for NCT06658899 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cardurion Pharmaceuticals, which has 9 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Catecholaminergic Polymorphic Ventricular Tachycardia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06658899 reports 9 study locations spanning 9 distinct geographic areas - top geographies include California, North Carolina, Texas.

Frequently Asked Questions

What is clinical trial NCT06658899 about?

NCT06658899 is a clinical study titled "A Phase 2 Study of CRD-4730 in CPVT". This is a Phase 2, multicenter, double-blind, sponsor blinded, placebo-controlled, repeat-dose clinical study of CRD-4730 to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of CRD-4730 to participants with Catecholaminergic Polymorphic Ventricular Tachycardia (CPV...

What is the current status of trial NCT06658899?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2025-12-01. Estimated completion is 2027-04.

What conditions does trial NCT06658899 study?

This clinical trial studies the following conditions: Catecholaminergic Polymorphic Ventricular Tachycardia.

What interventions are being tested in trial NCT06658899?

The interventions under investigation include: Placebo (DRUG), CRD-4730 (DRUG).

Who is sponsoring clinical trial NCT06658899?

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

Where is trial NCT06658899 being conducted?

This trial has 9 study locations across California, North Carolina, Texas, Wisconsin, British Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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