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RECRUITING
NCT06585449
PHASE1

A Study to Evaluate ALN-HTT02 in Adult Patients With Huntington's Disease

Sponsor: Alnylam Pharmaceuticals

View on ClinicalTrials.gov

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

Interventions

DRUG

ALN-HTT02

ALN-HTT02 will be administered intrathecally

DRUG

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