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A Study to Evaluate ALN-HTT02 in Adult Patients With Huntington's Disease
Sponsor: Alnylam Pharmaceuticals
Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of single or repeat doses of ALN-HTT02.
Official title: A Randomized, Double-blind, Placebo-controlled Study, to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intrathecally Administered Single Ascending Doses of ALN-HTT02 in Adult Patients With Huntington's Disease
Key Details
Gender
All
Age Range
25 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
66
Start Date
2024-10-14
Completion Date
2028-07-05
Last Updated
2026-03-31
Healthy Volunteers
No
Conditions
Interventions
ALN-HTT02
ALN-HTT02 will be administered intrathecally
Placebo
Placebo will be administered intrathecally
Locations (19)
Clinical Trial Site
Edmonton, Canada
Clinical Trial Site
Montreal, Canada
Clinical Trial Site
Ottawa, Canada
Clinical Trial Site
Vancouver, Canada
Clinical Trial Site
Berlin, Germany
Clinical Trial Site
Bochum, Germany
Clinical Trial Site
Bonn, Germany
Clinical Trial Site
Dresden, Germany
Clinical Trial Site
Münster, Germany
Clinical Trial Site
Taufkirchen, Germany
Clinical Trial Site
Ulm, Germany
Clinical Trial Site
Birmingham, United Kingdom
Clinical Trial Site
Cambridge, United Kingdom
Clinical Trial Site
Cardiff, United Kingdom
Clinical Trial Site
Glasgow, United Kingdom
Clinical Trial Site
Greater Manchester, United Kingdom
Clinical Trial Site
London, United Kingdom
Clinical Trial Site
Oxford, United Kingdom
Clinical Trial Site
Plymouth, United Kingdom