ClinicalTrials.gg
RecruitingNCT06658899CPVTUpdated Jul 9, 2026

A Phase 2 Study of CRD-4730 in CPVT

A Phase 2 interventional study of CRD-4730 and Placebo in Catecholaminergic Polymorphic Ventricular Tachycardia, sponsored by Cardurion Pharmaceuticals, Inc.. Recruiting at 12 sites in 6 countries. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Cardurion Pharmaceuticals, Inc. · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Dec 2025; still recruiting 11 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

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.

02

Conditions studied

  • Catecholaminergic Polymorphic Ventricular Tachycardia

Keywords

  • CaMKII
  • CPVT
  • Ventricular Tachycardia
  • CRD-4730
  • Cardiovascular
  • Arrhythmia
  • Catecholaminergic Polymorphic Ventricular Tachycardia
  • CaM kinase II
  • Calmodulin-dependent protein kinase II
03

In context

Tachycardia, Ventricular

451 studies on the registry are indexed under Tachycardia, Ventricular; 120 are open to participants now.

This study's planned enrollment of 12 is below the median of 71 across 280 interventional studies indexed under Tachycardia, Ventricular.

Browse Tachycardia, Ventricular studies →

Lead sponsor

Cardurion Pharmaceuticals, Inc. is the lead sponsor of 12 studies on the registry; 2 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 4 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Each participant must meet all the following criteria to be enrolled in this study:

  1. The participant is male or female, ≥18 years of age and of legal adult age in accordance with local requirements.
  2. The participant has a confirmed CPVT diagnosis, based on genetic screening for a pathogenic ryanodine receptor (RYR2) mutation and a clinical phenotype consistent with CPVT at Screening. Previous CPVT genetic testing documented in medical history is acceptable if confirmed by the Investigator and documented in the study source records.
  3. The participant can perform an EST during which frequent premature ventricular contractions (PVCs; ≥10 per minute), ventricular bigeminy, or higher-grade VA (equivalent to a VA score ≥2) are identified by the Investigator.
  4. The participant has been on a stable dose of at least 1 antiarrhythmic medication (including beta blockers but not amiodarone) for 4 weeks prior to Screening, unless the participant has been unable to tolerate antiarrhythmic therapy previously.
  5. Adheres to all criteria.

Exclusion criteria

Exclusion Criteria:

Participants meeting any of the following criteria will be excluded from the study:

  1. The participant has structural heart disease, diagnosis of heart failure, or clinically significant coronary artery disease.
  2. The participant has a clinically significant abnormal not explained by the diagnosis of CPVT at Screening or clinically significant abnormal intervals, such as prolonged .
  3. The participant has a history of a myocardial infarction, cerebrovascular accident, or within 3 months of Screening.
  4. The participant undergoes implantable cardioverter-defibrillator (ICD) implantation or has sympathetic nerve denervation within 3 months of Screening.
  5. The participant has an anticipated change in exercise regimen or new exercise program during the course of the study.
  6. The participant has a history of within the past 5 years at Screening, with the exception of successfully treated basal cell carcinoma or nonmetastatic squamous cell carcinoma of the skin or cervical carcinoma in situ. Prior exposure to chest radiation for any malignancy is exclusionary.
  7. The participant has abnormal blood pressure, defined as supine symptomatic hypotension, systolic blood pressure >150 mm Hg or diastolic blood pressure >90 mm Hg, or symptomatic bradycardia or a heart rate >100 bpm at Screening and/or on Day 1. Blood pressure and pulse should be measured after the participant has been in the seated position after 5 minutes of rest.
  8. The participant has hepatic impairment defined as (ALT) or aspartate aminotransferase (AST) >3 × ( [ULN]) and/or total >1.5 × ULN at Screening (unless secondary to confirmed Gilbert syndrome).
  9. The participant has acute or chronic (HBV; defined as hepatitis B surface antigen [HBsAg] reactive), acute or chronic virus (HCV; defined as detection of HCV antibody and RNA [qualitative]), or (HIV) infection.
  10. The female participant is pregnant, lactating/breastfeeding, or has plans to become pregnant during the study or within 3 months following the last study drug administration.
  11. The participant has taken any antiarrhythmic drug in addition to their stable, chronic regimen unless it has been at least 5 half-lives since administration at the time of Screening.
Terms in these criteria, in plain language(12)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
12 participants (estimated)

Study arms

  • Experimental
    Dose 1

    CRD-4730 Dose 1 Tablet

    Drug: CRD-4730

  • Experimental
    Dose 2

    CRD 4730 Dose 2 Tablet

    Drug: CRD-4730

  • Placebo comparator
    Dose 3

    Placebo tablet to match CRD-4730

    Drug: Placebo

Interventions

  • Oral CRD-4730 in tablet form

  • DrugPlacebo

    Placebo to match CRD-4730 in tablet form

06

What researchers measure

Primary outcomes

  1. Primary Outcome Measures

    The number and severity of treatment-emergent adverse events (TEAEs) related to study drug treatment

    Time frame: Baseline to Day 101

Secondary outcomes

  1. Secondary Outcome Measure

    Change in VA score during EST from baseline to Day 15, from baseline to Day 44, and from baseline to Day 73

    Time frame: Baseline to Day 15; Baseline to Day 44; Baseline to Day 73

  2. Secondary Outcome Measures

    Plasma concentrations of CRD-4730 over time for each treatment period

    Time frame: Baseline to Day 15; Baseline to Day 44; Baseline to Day 73

07

Study locations

12 of 12 sites recruiting
  • Cardurion Investigative Site
    San Francisco, California 94143, United States
    Recruiting
  • Cardurion Investigative Site
    Morrisville, North Carolina 27560, United States
    Recruiting
  • Cardurion Investigative Site
    Houston, Texas 77030, United States
    Recruiting
  • Cardurion Investigative Site
    Salt Lake City, Utah 84113, United States
    Recruiting
  • Cardurion Investigative Site
    Madison, Wisconsin 53792, United States
    Recruiting
  • Cardurion Investigative Site
    Vancouver, British Columbia V6Z 1Y6, Canada
    Recruiting
  • Cardurion Investigative Site
    Bron, 69677, France
    Recruiting
  • Cardurion Investigative Site
    Paris, 75018, France
    Recruiting
  • Cardurion Investigative Site
    Saint-Herblain, 44800, France
    Recruiting
  • Cardurion Investigative Site
    Pavia, Pavia 27100, Italy
    Recruiting
  • Cardurion Investigative Site
    Amsterdam, North Holland 1105 AZ, Netherlands
    Recruiting
  • Cardurion Investigative Site
    Esplugues de Llobregat, Barcelona 08950, Spain
    Recruiting
08

References and documents

Publications

  • Takagahara, Shuichi, et al. "Novel, Potent, and Highly Selective Calcium/Calmodulin-Dependent Protein Kinase II (CaMKII) Inhibitors Reduce Substrate Phosphorylation in Rat Hearts and Prolong Survival in a Mouse Model of Severe Heart Failure." Circulation 148.Suppl_1 (2023): A12726-A12726.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06658899
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Responsible party
Sponsor
First posted
Oct 26, 2024
Start date
Dec 1, 2025
Primary completion
Apr 2027 (estimated)
Completion
Apr 2027 (estimated)
Last update
Jul 9, 2026

Study contacts

Cardurion
Contact
infoCPVT@cardurion.com
617-863-8088

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: CRD-4730

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