ClinicalTrials.gg
TerminatedNCT06005428CPVTUpdated May 27, 2026

Effectiveness of CRD-4730 in Participants With Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

A Phase 2 interventional study of CRD-4730 and Placebo in CPVT1, Heart Defects, Congenital and Heart Diseases, sponsored by Cardurion Pharmaceuticals, Inc.. Terminated at 11 sites in 4 countries. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-05-27.

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

Why this study was terminated
The early termination of the clinical trial is due to an internal administrative and business decision, the study is not being terminated for safety reasons.

From the registry’s dates

  • Primary completion was May 2025, 1 year 5 months ago, and no results have been posted to the registry; the sponsor requested a delay in submitting them in May 2026.
Phase
Phase 2
Study type
Interventional
Enrollment
7
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

Study summary

This is a Phase 2, multicenter, double-blind, sponsor unblinded, placebo-controlled, single-dose clinical study of CRD-4730 to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of CRD-4730 when administered as single oral doses to participants with Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). The study will have 2 cohorts in which participants with CPVT will participate in a 3-period, randomized 2-sequence study. Each participant will receive 2 different doses of CRD-4730 and 1 dose of matching placebo, with each study drug administered as a single dose.

02

Conditions studied

  • CPVT1
  • Heart Defects, Congenital
  • Heart Diseases
  • Ventricular Tachycardia

Keywords

  • CaMKII
  • Catecholaminergic polymorphic VT
  • Ventricular Tachycardia
  • CRD-4730
03

In context

Heart Defects, Congenital

991 studies on the registry are indexed under Heart Defects, Congenital; 251 are open to participants now.

This study's enrollment of 7 is below the median of 60 across 507 interventional studies indexed under Heart Defects, Congenital.

Browse Heart Defects, Congenital 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

  1. Males or Females ≥18 years of age, at screening.
  2. Confirmed CPVT diagnosis, based on genetic screening for a known RyR2 mutation and a clinical phenotype consistent with CPVT at screening.
  3. The participant can perform an EST during which frequent premature ventricular contraction (PVCs) (≥10 per minute), ventricular bigeminy, or higher-grade VA (equivalent to a VA score ≥2) are identified by the investigator.
  4. Stable doses of any anti-arrhythmic medication, except amiodarone, for 4 weeks prior to screening.
  5. Adhere to all criteria.

Exclusion criteria

Exclusion Criteria:

  1. structural heart disease, diagnosis of heart failure, or clinically significant coronary artery disease.
  2. History of a myocardial infarction, cerebrovascular accident, or within 3 months of screening.
  3. History of within the past 5 years at screening (except successfully treated basal cell carcinoma or non- squamous cell carcinoma of the skin or cervical carcinoma in situ).
  4. Female participant that is pregnant or lactating/ breastfeeding, or has plans to do so during the study or within 3 months following last dose of study drug.
  5. Use of amiodarone with 3 months prior to screening. NOTE: other protocol defined Inclusion/ Exclusion criteria may apply.
Terms in these criteria, in plain language(5)

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.

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.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

05

Study design

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

Study arms

  • Experimental
    Dose 1

    CRD-4730 Dose 1 capsule

    Drug: CRD-4730

  • Experimental
    Dose 2

    CRD-4730 Dose 2 capsule

    Drug: CRD-4730

  • Placebo comparator
    Dose 3

    Placebo capsule to match CRD-4730

    Drug: Placebo

Interventions

  • Oral CRD-4730 in capsule form

  • DrugPlacebo

    Placebo to match CRD-4730 in capsule form

06

What researchers measure

Primary outcomes

  1. Treatment Emergent Adverse Events (TEAEs)

    The number of participants with TEAEs including drug-related AEs, serious AEs (SAEs), and AEs leading to study drug discontinuation will be assessed.

    Time frame: Baseline to Day 22

  2. Changes in Laboratory Assessments

    The number of participants who have normal/ abnormal values at Baseline compared to normal/ abnormal values post-Baseline will be assessed for hematology, serum chemistry and urinalysis.

    Time frame: Baseline to Day 15

  3. Changes in Vital Signs Measurement: Systolic and Diastolic blood pressure

    Percent change from Baseline to post Baseline will be assessed for systolic and diastolic blood pressure

    Time frame: Baseline to Day 15

  4. Changes in Vital Signs Measurement: Pulse Rate

    Percent change from Baseline to post Baseline will be assessed for pulse rate

    Time frame: Baseline to Day 15

  5. Changes in Vital Signs Measurement: Respiratory Rate

    Percent change from Baseline to post Baseline will be assessed for respiratory rate

    Time frame: Baseline to Day 15

  6. Changes in Vital Signs Measurement: Body Temperature

    Percent change from Baseline to post Baseline will be assessed for body temperature

    Time frame: Baseline to Day 15

  7. Changes in Physical Exam

    General physical exams will be carried out to detect any abnormalities in the cardiovascular, respiratory and other body systems

    Time frame: Baseline to Day 22

  8. Changes in Electrocardiogram (ECG) Measurements

    Number of participants who have normal/abnormal ECG measurements at Baseline will be compared to normal/abnormal ECG measurement post Baseline

    Time frame: Baseline to Day 22

Secondary outcomes

  1. Change in Ventricular Arrhythmia (VA) score during Exercise Stress Test (EST)

    The VA score is a physician administered score on a scale of 0-5 with higher numbers being worse.

    Time frame: Baseline to Day 1

  2. Change in Ventricular Arrhythmia (VA) score during Exercise Stress Test (EST)

    The VA score is a physician administered score on a scale of 0-5 with higher numbers being worse.

    Time frame: Baseline to Day 8

  3. Change in Ventricular Arrhythmia (VA) score during Exercise Stress Test (EST)

    The VA score is a physician administered score on a scale of 0-5 with higher numbers being worse.

    Time frame: Baseline to Day 15

  4. Assessment of PK effect

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

    Time frame: Baseline through Day 15

07

Study locations

11 sites
  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio 45229, United States
  • Cleveland Clinic Children's Hospital
    Cleveland, Ohio 44195, United States
  • Baylor College of Medicine
    Houston, Texas 77030, United States
  • Stollery Children's Hospital University of Alberta
    Edmonton, Alberta T6G 2R7, Canada
  • University of British Columbia (UBC) Hospital
    Vancouver, British Columbia V5Z 1M9, Canada
  • British Columbia Children's Hospital
    Vancouver, British Columbia V6H 3N1, Canada
  • University of Western Ontario
    London, Ontario N6A 5A5, Canada
  • Hôptal Nord Laennec
    Nantes, Loire-Atlantique 44805, France
  • Hôpital Louis Pradel
    Bron, 69677, France
  • Groupe Hospitalier Bichat Claude Bernard
    Paris, 75018, France
  • IRCCS Pavia Istituti Clinici Scientifici Maugeri Spa Società Benefit
    Pavia, Lombardy 27100, Italy
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06005428
Lead sponsor
Cardurion Pharmaceuticals, Inc.
Responsible party
Sponsor
First posted
Aug 22, 2023
Start date
Nov 7, 2023
Primary completion
May 31, 2025
Completion
May 31, 2025
Last update
May 27, 2026

Study contacts

Jason Homsy, M.D., Ph.D.
study director · Executive Medical Director

Oversight

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

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This study is terminated, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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