drugset / Trial / NCT06681766

A Study to Assess Nomlabofusp in Adolescents and Children With Friedreich's Ataxia

NCT06681766 ↗

Phase 1 Terminated 18 enrolled Larimar Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

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).

Timeline

Start
2024-12-06
Primary completion
2025-04-27
Completion
2025-04-27

Outcome

Outcome not reported

Stopped (Enrollment): “Review of Cohort 1 data facilitated direct enrollment into open label study and eliminate pause in study drug administration between PK study and open label study.”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Nomlabofusp Protein / enzyme biologic 0.8 mg/kg Subcutaneous

Indications