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NCT Number: NCT07180355

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.

Recruiting

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Has history of FA symptom onset ≤25 years of age
  • Has a clinical and genetic diagnosis of FA
  • Has a staging score of ≥1 but <6 on the Friedreich's Ataxia Rating Scale (FARS) Functional Disability Staging Score
  • Is willing to agree to the following rules for use of omaveloxolone (Skyclarys):
  • For a candidate who is currently taking omaveloxolone, has been on a stable dose for 12 weeks, expects to continue taking omaveloxolone at that dose throughout the study, and is willing to stop taking omaveloxolone at the direction of the Investigator or Sponsor's Medical Monitor if evidence of transaminitis or synthetic liver dysfunction is detected during the study
  • For a candidate who is not actively taking omaveloxolone, at least 12 weeks have passed since the last dose and the candidate agrees not to resume omaveloxolone during the 18-month period after SGT-212 infusion NOTE: The use of any other approved or investigational medicinal product for the treatment of FA should be discussed with the study team.

Exclusion criteria

  • Antibodies against adeno-associated virus serotype 9 (AAV9)
  • Has a modified FARS (mFARS) score <20
  • Has a body weight ≤25 kilogram (kg) or has body mass index (BMI) ≥33 kg/m^2
  • Has a contraindication to endomyocardial biopsy (EMB) or cardiac catheterization
  • Is unable to undergo cardiac and brain MRI with contrast, including hypersensitivity to gadolinium contrast agent, presence of a non-MRI-compatible cardiac pacemaker, presence of a non-MRI-compatible implantable cardiac defibrillator, or physical condition (e.g., contractures)
  • Has uncontrolled diabetes as defined by a hemoglobin (Hb) A1c >9%
  • Has participated in recent interventional clinical studies or received any investigational therapy administered within 3 months or 5 half-lives (whichever is longer) prior to Screening
  • Has received gene therapy at any time
  • Has contraindications to receiving corticosteroids
  • Has any contraindication to the surgical procedures involved with IDN infusion of SGT-212
  • Has any known cardiac disease not related to FA including known obstructive coronary artery disease (CAD)
  • Other Inclusion/Exclusion criteria to be applied as per protocol.

Treatment and study plan

SGT-212

Drug

Adeno-associated virus serotype AAVhu68 containing a codon-optimized complementary DNA (cDNA)

Primary outcomes

  1. Incidence and Severity of Treatment Emergent Adverse Events (TEAEs)

    Time frame: Month 12

Secondary outcomes

  1. Incidence and Severity of TEAEs

    Time frame: Months 18 and 60

  2. Incidence and Severity of Treatment-emergent Serious adverse events (SAEs)

    Time frame: Months 18 and 60

  3. Number of Treatment-emergent deaths

    Time frame: Months 18 and 60

  4. Change from Baseline in Columbia-Suicide Severity Rating Scale (C-SSRS)

    Time frame: Baseline, Months 18 and 60

  5. Number of Participants with Change from Baseline in Significant Abnormalities in Laboratory Tests

    Time frame: Baseline, Months 18 and 60

  6. Number of Participants with Change from Baseline in Significant Abnormalities in Vital Signs

    Time frame: Baseline, Months 18 and 60

  7. Number of Participants with Change from Baseline in Significant Abnormalities in Physical Examination Findings

    Time frame: Baseline, Months 18 and 60

  8. Number of Participants with Change from Baseline in Innate and Adaptive Immune Responses

    Time frame: Baseline, Months 18 and 60

  9. Change from Baseline in Blood Biomarkers Including Inflammatory Markers

    Time frame: Baseline, Month 12

Study contacts

Contact information is provided by the study sponsor or research team.

Solid Biosciences Clinical Trials

CONTACT

[email protected]

+1617-337-4680

Sponsors and collaborators

Lead sponsor

Solid Biosciences Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2028
Study completion
2032
First posted
Sep 18, 2025
Registry last updated
Jul 30, 2026

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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