Open-label, Dose Escalation Study of Safety and Preliminary Efficacy of TN-401 in Adults With PKP2 Mutation-associated ARVC

Part of paid clinical trials in San Francisco, California.

Sponsor
Tenaya Therapeutics
Study ID
NCT06228924
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • TN-401 — GENETIC
    TN-401 is a recombinant adeno-associated virus serotype 9 (AAV9) gene therapy containing Plakophilin-2 (PKP2) transgene. It is a single (one-time) intravenous dose.

Study Details

This first-in-human study is designed to evaluate the safety, and preliminary efficacy (PD) of TN-401 gene therapy in adult patients with symptomatic PKP2 mutation-associated ARVC.

Key Dates

First listed
Jan 29, 2024
Start date
Mar 26, 2024
Status verified
Sep 2024
Primary completion
May 1, 2026
Completion
Oct 1, 2029

Study Design

Enrollment
15 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: Cohort 1
    Dose for Cohort 1 will be 3E13 vg/kg
  • Experimental: Cohort 2
    Dose for Cohort 2 will be 6E13 vg/kg

Primary Outcome Measure

Number and severity of Adverse Events over the course of the study. [ Time Frame: 52 weeks ]

Central Contacts

Locations (7)

FacilityCityStateZIPSite coordinators
University of California San FranciscoSan FranciscoCalifornia94143
Vasanth Vedantham, MD
University of Colorado - Anschutz Medical CampusAuroraColorado80045
Matthew Taylor, MD
Johns Hopkins UniversityBaltimoreMaryland21287
Andreas Barth, MD (PRINCIPAL_INVESTIGATOR)
Brigham and Women's HospitalBostonMassachusetts02115
Neal Lakdawala, MD
Mayo ClinicRochesterMinnesota55905
John R. Giudicessi, MD (PRINCIPAL_INVESTIGATOR)
NYU Langone HealthNew YorkNew York10016
Larry Chinitz, MD
Cleveland ClinicClevelandOhio44195
Milind Desai, MD

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