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NCT06826612PHASE1, PHASE2Recruiting

A Randomized Study of SPK-10001 Gene Therapy in Participants With Huntington's Disease

Hoffmann-La Roche

Start Date

2/21/2025

Completion Date

1/12/2035

Summary

The main goal of this study is to evaluate the safety, tolerability, and preliminary efficacy of SPK-10001 in participants with Huntington's Disease.

Eligibility Criteria

Age Range: 25 years to 65 years

Key Inclusion Criteria: * Have confirmed huntingtin (HTT) cytosine-adenine-guanine (CAG) repeat length ≥40 on genetic testing and confirmation diagnostic test by the central laboratory (CL) at screening. * Have striatal atrophy demonstrated by caudate/intracranial volume less than the age-adjusted cutoff values associated with HDISS Stage 1. * Have UHDRS Total Motor Score (TMS) equal to or greater than the age-adjusted cutoff value associated with HDISS Stage 2. * Have UHDRS Total Functional Capacity (TFC) greater than or equal to 11. * Use of cholinesterase inhibitors, memantine, amantadine, or riluzole must have been at stable dosing for at least 12 weeks before screening and baseline and anticipated to remain stable during the first 12 months after SPK-10001 administration. * Antidepressant or benzodiazepine use must have been at stable dosing for at least 12 weeks before screening and baseline and anticipated to remain stable during the first 12 months after SPK-10001 administration. * Antipsychotics for motor symptoms or mood stabilization (i.e., irritability or aggressive behavior) and/or tetrabenazine, valbenazine, or deutetrabenazine must have been at a stable dose for at least 12 weeks before screening and baseline and are anticipated to remain stable during the first 12 months after SPK-10001 administration. Key Exclusion Criteria: * A safe trajectory is not able to be identified for targeting placement of the cannula into the caudate or putamen on both sides of the brain due to extent of atrophy or other anatomical features. * Have received an antisense oligonucleotide therapy during the past year. * History of deep brain stimulation. * History of or intention to undergo gene therapy, cell transplantation, or brain surgery during the course of the study. * Have participated in an investigational drug study with a systemic administration within 6 weeks or 5 half-lives of screening, whichever is longer. Additional protocol-defined inclusion/exclusion criteria apply.

Interventions

GENETIC

SPK-10001

OTHER

Placebo Surgery Control

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Conditions

Huntington Disease

Locations

Beth Israel Deaconess Medical Center

Boston, Massachusetts 02215

United States

University of Cincinnati/Cincinnati Children's Hospital

Cincinnati, Ohio 45221

United States

Ohio State University

Columbus, Ohio 43221

United States

University of Pennsylvania

Philadelphia, Pennsylvania 19107

United States

University of Pittsburg

Pittsburgh, Pennsylvania 15213

United States