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Study identifier: NCT06658899 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Phase 2 Study of CRD-4730 in CPVT

Condition: Catecholaminergic Polymorphic Ventricular Tachycardia  ·  Sponsor: Cardurion Pharmaceuticals, Inc.

PhasePhase 2
Planned participants12
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

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

Always discuss trial participation with your own doctor first.

Locations (12)

Cardurion Investigative SiteSan Francisco, California, United StatesRecruiting
Cardurion Investigative SiteMorrisville, North Carolina, United StatesRecruiting
Cardurion Investigative SiteHouston, Texas, United StatesRecruiting
Cardurion Investigative SiteSalt Lake City, Utah, United StatesRecruiting
Cardurion Investigative SiteMadison, Wisconsin, United StatesRecruiting
Cardurion Investigative SiteVancouver, British Columbia, CanadaRecruiting
Cardurion Investigative SiteBron, FranceRecruiting
Cardurion Investigative SiteParis, FranceRecruiting
Cardurion Investigative SiteSaint-Herblain, FranceRecruiting
Cardurion Investigative SitePavia, Pavia, ItalyRecruiting
Cardurion Investigative SiteAmsterdam, North Holland, NetherlandsRecruiting
Cardurion Investigative SiteEsplugues de Llobregat, Barcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06658899