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Clinical Trials in the USA / NCT06826612
Recruiting Phase 1/2

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

NCT06826612 · tracked via the Priya Life Science USA tracker
Sponsor
Hoffmann-La Roche
Phase
Phase 1/2
Started
2025-02-21
Last updated
2026-05-05

Condition(s) studied

Huntington Disease

Investigational drug(s) / intervention(s)

SPK-10001Placebo Surgery Control

SPK-10001: Specified dose on specified days

Placebo Surgery Control: Placebo Surgery procedure for SPK-10001

Study 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

Sex
ALL
Min age
25 Years
Max age
65 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Beth Israel Deaconess Medical Center Boston Massachusetts Recruiting
University of Cincinnati/Cincinnati Children's Hospital Cincinnati Ohio Recruiting
Ohio State University Columbus Ohio Recruiting
University of Pennsylvania Philadelphia Pennsylvania Recruiting
University of Pittsburg Pittsburgh Pennsylvania Recruiting

More Hoffmann-La Roche trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06826612 on ClinicalTrials.gov ↗ ← All trials in the USA