Trial intelligence / Profile preview

Dalfampridine in Hereditary Spastic Paraplegia

NCT05613114Completed

Sponsor
European University of Lefke
Start
Aug 2020
Primary completion
Mar 2021
Modality
Small Molecules
Countries
1
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Overview

Randomised, triple-blind trial in hereditary spastic paraplegia (HSP) comparing Dalfampridine + Physiotherapy with Placebo + Physiotherapy (2 arms). Primary endpoint: Timed 25-foot Walk Test at 8 weeks. Started Aug 2020; status: completed.

02

Drugs

dalfampridine
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Conditions

hereditary spastic paraplegia (HSP)

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