drugset / Trial / NCT01411150

Premanifest Huntington's Disease: Creatine Safety & Tolerability Extension Study

NCT01411150

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this clinical trial is to extend the Pre-Crest study (Protocol # (NCT00592995) to further assess the long-term safety and tolerability of up to 30 grams daily creatine in individuals at-risk for Huntington's Disease (HD) and to assess whether biomarkers responsive to creatine in symptomatic individuals are informative in premanifest individuals over a longer duration.

Timeline

Start
2009-05
Primary completion
2012-09
Completion
2012-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Creatine Other / unclassified 30 g

Indications