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NCT06681766 · ClinicalTrials.gov registry record · Phase 1
A Study to Assess Nomlabofusp in Adolescents and Children With Friedreich's Ataxia
A Phase 1 study, sponsored by Larimar Therapeutics.
- Terminated
- Registry status
- Phase 1
- Development phase
- 18
- Enrollment target
NCT06681766: Clinical Trial Phase 1 study, sponsored by Larimar Therapeutics.
NCT06681766 is a Phase 1 study that was terminated before completion, run by Larimar Therapeutics. The registered enrollment target is 18 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06681766, a Phase 1 study, was terminated before completion, sponsored by Larimar Therapeutics.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 18 participants
- Enrollment target
Study Summary
The goal of this clinical trial is to evaluate the safety and tolerability of nomlabofusp (CTI-1601) in adolescents and children with Friedreich's ataxia (FRDA).
Primary Outcome
Number
Interventions
- DRUG Placebo
- DRUG Nomlabofusp
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2024-12-06 |
| Est. Completion | 2025-04-27 |
| Phase | Phase 1 |
Why NCT06681766 stopped before completion
NCT06681766 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT06681766 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06681766 about?
NCT06681766 is a clinical study titled "A Study to Assess Nomlabofusp in Adolescents and Children With Friedreich's Ataxia". The goal of this clinical trial is to evaluate the safety and tolerability of nomlabofusp (CTI-1601) in adolescents and children with Friedreich's ataxia (FRDA).
What is the current status of trial NCT06681766?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2024-12-06. Estimated completion is 2025-04-27.
What interventions are being tested in trial NCT06681766?
The interventions under investigation include: Placebo (DRUG), Nomlabofusp (DRUG).
Who is sponsoring clinical trial NCT06681766?
This trial is sponsored by Larimar Therapeutics, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06681766's enrollment target sits among peer trials
18 1720th of 2000 higher than 216 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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