Riluzole in Patients With Spinocerebellar Ataxia Type 7

PHASE2/PHASE3RecruitingINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

June 1, 2021

Primary Completion Date

September 1, 2025

Study Completion Date

September 1, 2026

Conditions
SCA7
Interventions
DRUG

Riluzole

Study drug will be orally dispensed in doses of 50 mg twice daily for 12 months in the treated group.

DRUG

Placebo

Placebo drug for 6 months, however they will receive riluzole during the last 6 months of study, so that all patients will undergo the active drug in the last phase of the study.

Trial Locations (1)

00139

RECRUITING

"Neurological Unit, S. Andrea Hospital, Faculty of Medicine and Psychology, Sapienza University of Rome", Rome

All Listed Sponsors
lead

S. Andrea Hospital

OTHER