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Tolerability and Efficacy of L-Serine in Patients With Amyotrophic Lateral Sclerosis (ALS) — ALS  

Amyotrophic Lateral Sclerosis (ALS) Clinical Trial

Official title:
Tolerability and Efficacy of L-Serine in Patients With Amyotrophic Lateral Sclerosis: A Phase IIa Study

Clinical Trial Summary

The purpose of this study is to determine the tolerability of L-Serine oral doses for ALS patients and assess preliminary indications of efficacy

Clinical Trial Description

All patients will receive the same dose of the study treatment over 6 months. For each participant the study will last approximately one year with follow up visits after the treatment period of 6 months is completed. The visits will include blood draws, vital sign checks, neurological and physical exams, pulmonary testing with forced vital capacity (FVC), and questionnaires. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03580616
Study type Interventional
Source Dartmouth-Hitchcock Medical Center
Contact
Status Terminated
Phase Phase 2
Start date October 24, 2018
Completion date December 20, 2022
View Details
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