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NCT07148089 · ClinicalTrials.gov registry record · Phase 1

A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

A Phase 1 study of Catecholaminergic Polymorphic Ventricular Tachycardia, sponsored by Solid Biosciences.

Recruiting
Registry status
Phase 1
Development phase
18
Enrollment target
5
Study locations

NCT07148089 is a Phase 1 study of Catecholaminergic Polymorphic Ventricular Tachycardia that is actively recruiting participants, run by Solid Biosciences. The registered enrollment target is 18 participants. The trial reports 5 study locations across 5 states.

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The verdict

NCT07148089, a Phase 1 study of Catecholaminergic Polymorphic Ventricular Tachycardia, is actively recruiting participants, sponsored by Solid Biosciences.

RECRUITING
Registry status
Phase 1
Development phase
18 participants
Enrollment target
5
Study locations

Study Summary

This is a Phase 1b, Multicenter, Open-Label, Dose Finding Study to Investigate the Safety and Tolerability of a Single Intravenous Dose of SGT-501 in participants with catecholaminergic polymorphic ventricular tachycardia (CPVT). The first-in-human (FIH) safety study will focus on obtaining safety data in adult participants. Cohort 1 and Cohort 2 (optional for dose exploration) will include participants ≥ 18 years of age. Cohort 3 will include participants ≥ 7 to \< 18 years of age and will be initiated following data and safety monitoring board (DSMB) recommendations. Participants will be monitored for 5 years post-administration of SGT-501 including the active treatment period (1 year) and long-term follow-up (LTFU) (4 years) period.

Interventions

  • DRUG SGT-501

Study Locations (5)

Massachusetts

  • Boston Children's Hospital - Boston

Minnesota

  • Mayo Clinic - Rochester

Ohio

  • Cleveland Clinic - Cleveland

Pennsylvania

  • University of Pennsylvania - Philadelphia

British Columbia

  • St. Paul's Hospital - Vancouver

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2026-02-23
Est. Completion 2031-05
Phase Phase 1

Sponsor

Solid Biosciences

6 total trials

What the Registry Record Tells You About NCT07148089

The ClinicalTrials.gov registry entry for NCT07148089 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Solid Biosciences, which has 6 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 1 intervention - of which SGT-501 is the first listed.

NCT07148089 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Massachusetts, Minnesota, Ohio.

Frequently Asked Questions

What is clinical trial NCT07148089 about?

NCT07148089 is a clinical study titled "A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)". This is a Phase 1b, Multicenter, Open-Label, Dose Finding Study to Investigate the Safety and Tolerability of a Single Intravenous Dose of SGT-501 in participants with catecholaminergic polymorphic ventricular tachycardia (CPVT). The first-in-human (FIH) safety study will focus on obtaining safety d...

What is the current status of trial NCT07148089?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2026-02-23. Estimated completion is 2031-05.

What conditions does trial NCT07148089 study?

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

What interventions are being tested in trial NCT07148089?

The interventions under investigation include: SGT-501 (DRUG).

Who is sponsoring clinical trial NCT07148089?

This trial is sponsored by Solid Biosciences, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07148089 being conducted?

This trial has 5 study locations across Massachusetts, Minnesota, Ohio, Pennsylvania, British Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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