drugset / Trial / NCT02118727

Therapy in Amyotrophic Lateral Sclerosis (TAME)

NCT02118727

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if memantine at up to 20 mg twice a day when used in conjunction with riluzole, can slow down the disease progression of patients with ALS including potentially improving their neuropsychiatric changes, as well as determine if serum biomarkers can be used both as a diagnostic and a prognostic marker in patients with ALS. Funding Source: FDA - Orphan Products Development (OPD)

Timeline

Start
2018-11-07
Primary completion
2021-07-22
Completion
2021-07-22

Drugs

EvaluationDrugModalityDoseRoute
Comparator Memantine Unknown 20 mg Oral