drugset / Trial / NCT02118727
Therapy in Amyotrophic Lateral Sclerosis (TAME)
Phase 2
Completed
89 enrolled
University of Kansas Medical Center
University of Missouri-Columbia · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Memantine | Unknown | 20 mg | Oral |