SGT-212
DrugAdeno-associated virus serotype AAVhu68 containing a codon-optimized complementary DNA (cDNA)
NCT Number: NCT07180355
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.
Interested in participating?
Request Info18 year–40 year
All sexes
Interventional
Phase 1
The University of California, Los Angeles (UCLA), Los Angeles, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Adeno-associated virus serotype AAVhu68 containing a codon-optimized complementary DNA (cDNA)
Time frame: Month 12
Time frame: Months 18 and 60
Time frame: Months 18 and 60
Time frame: Months 18 and 60
Time frame: Baseline, Months 18 and 60
Time frame: Baseline, Months 18 and 60
Time frame: Baseline, Months 18 and 60
Time frame: Baseline, Months 18 and 60
Time frame: Baseline, Months 18 and 60
Time frame: Baseline, Month 12
Contact information is provided by the study sponsor or research team.
Solid Biosciences Inc.
Industry
A Phase 1b First-in-Human, Open-Label, Dose-Finding Trial to Evaluate the Safety and Tolerability of SGT-212 Delivered Via Dual Intradentate Nucleus (IDN) and Intravenous (IV) Administration to Participants With Friedreich's Ataxia (FA)
Acronym: FALCON
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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