Friedreich's Ataxia

Clinical trial pipeline · Data from ClinicalTrials.gov

See which Friedreich's Ataxia trials you may qualify for

Total trials

Actively recruiting

Phase 3 trials

Completed

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

RecruitingNot Applicable

NCT01793168

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, i…

United States, Australia20,000 participantsStarted 2010-07

All recent trials (2 shown)

CompletedNot Applicable

NCT07123142

FRIEDREICH ATAXIA- STEROIDOGENESIS

Friedreich's ataxia (FA) is a rare autosomal recessive disorder caused by GAA repeat expansion in the FXN gene, leading to impaired iron-sulfur (Fe-S) cluster b…

Turkey (Türkiye)25 participantsStarted 2025-05-01

Friedreich&#39;s Ataxia

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

All recent trials (2 shown)

FRIEDREICH ATAXIA- STEROIDOGENESIS

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

All recent trials (2 shown)

FRIEDREICH ATAXIA- STEROIDOGENESIS

Friedreich's Ataxia