A Phase 2 Study of CRD-4730 in CPVT
Part of paid clinical trials in San Francisco, California.
- Sponsor
- Cardurion Pharmaceuticals, Inc.
- Study ID
- NCT06658899
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Catecholaminergic Polymorphic Ventricular Tachycardia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Not accepted
Interventions
- CRD-4730 — DRUGOral CRD-4730 in tablet form
- Placebo — DRUGPlacebo to match CRD-4730 in tablet form
Study Details
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.
Key Dates
- Start date
- Dec 1, 2025
- Status verified
- Nov 2025
- Primary completion
- Apr 30, 2027
- Completion
- Apr 30, 2027
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Experimental: Dose 1CRD-4730 Dose 1 Tablet
- Experimental: Dose 2CRD 4730 Dose 2 Tablet
- Placebo Comparator: Dose 3Placebo tablet to match CRD-4730
Primary Outcome Measure
Primary Outcome Measures [ Time Frame: Baseline to Day 101 ]
Central Contacts
- Jason Homsy, MD, Ph.D.617-863-8088
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cardurion Investigative Site | San Francisco | California | 94143 | - |
| Cardurion Investigative Site | Morrisville | North Carolina | 27560 | - |
| Cardurion Investigative Site | Houston | Texas | 77030 | - |
| Cardurion Investigative Site | Madison | Wisconsin | 53792 | - |
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