drugset / Trial / NCT06447025

An Open-Label Study of CTI-1601 in Subjects With Friedreich's Ataxia

NCT06447025 ↗

Phase 2 Recruiting 85 enrolled Larimar Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

An open label study designed to evaluate the safety, PK, PD, and clinical effects of long-term daily administration of CTI-1601 enrolling adolescent and adult patients with FRDA who have participated in a prior clinical study of CTI-1601 as well as children (age 2 years and older), adolescents and adults with FRDA who have not participated in a prior clinical study of CTI-1601.

Timeline

Start
2024-01-25
Primary completion
2027-01
Completion
2027-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Nomlabofusp Protein / enzyme biologic 0.8 mg/kg Subcutaneous
Subject Nomlabofusp Protein / enzyme biologic 50 mg Subcutaneous

Indications