Apply to trial NCT07180355

A few quick questions so the study team can decide if you might be a fit.

RecruitingPhase 1Drug trial

A Study of SGT-212 Gene Therapy in Friedreich's Ataxia

This is a phase 1b, first in-human, open-label, dose-finding study investigating the safety and tolerability of SGT-212 in participants with Friedreich's ataxia (FA). It will be delivered via dual intradentate nucleus (IDN) and intravenous (IV) administration to participants with FA. All participants will receive SGT-212 and will be enrolled in the study for approximately 5 years.

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A Study of SGT-212 Gene Therapy in Friedreich's Ataxia

How this works

Answer a few questions

We connect you with the study team

The team reaches out to schedule screening