The main goal of this study is to evaluate the safety, tolerability, and preliminary efficacy of SPK-10001 in participants with Huntington's Disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
53
Specified dose on specified days
Placebo Surgery procedure for SPK-10001
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States
RECRUITINGUniversity of Cincinnati/Cincinnati Children's Hospital
Cincinnati, Ohio, United States
RECRUITINGOhio State University
Columbus, Ohio, United States
Number of Participants with Treatment-emergent Adverse Events (TEAEs)
Time frame: Day 1 up to approximately 5 years
Severity of TEAEs
Time frame: Day 1 up to approximately 5 years
Change from Baseline in Unified Huntington's Disease Rating Scale (UHDRS®) Total Functional Capacity (TFC) Score
Time frame: Baseline, Month 24
Change from Baseline in Motor Symptom Progression Based on Huntington's Disease Digital Motor Score (HDDMS)
Time frame: Baseline, Months 12, 18, and 24
Change from Baseline in Composite UHDRS (cUHDRS) Score
Time frame: Baseline, Months 12, 18, and 24
Change from Baseline in UHDRS TFC Score
Time frame: Baseline, Months 12 and 18
Reference Study ID Number: SPK-10001-101 https://forpatients.roche.com/
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of Pennsylvania
Philadelphia, Pennsylvania, United States
RECRUITINGUniversity of Pittsburg
Pittsburgh, Pennsylvania, United States
RECRUITING