drugset / Trial / NCT00140218

R(+) Pramipexole in Early Amyotrophic Lateral Sclerosis

NCT00140218

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The hypothesis of this study is that treatment with R(+) pramipexole at 30 mg/day will alter the slope of decline in ALS functional rating scale over the course of 6 months. ALS patients at an early stage of disease will be observed for 3 months after enrollment and then treated with drug for 6 months.

Timeline

Start
2005-08
Primary completion
2007-01
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramipexole Unknown 10 mg Oral