Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Subcutaneous Nomlabofusp in Subjects With Friedreich's Ataxia source ↗
Raise Follow-on offering: $100M (total, as published), announced Feb 26, 2026. Source: company release on GlobeNewswire. source ↗
Raise Follow-on offering: $69M (total, as published), announced Jul 31, 2025. Source: company release on GlobeNewswire. source ↗
Trial start Phase 1: A Study to Assess Nomlabofusp in Adolescents and Children With Friedreich's Ataxia source ↗
Trial start Phase 2: An Open-Label Study of CTI-1601 in Subjects With Friedreich's Ataxia source ↗
Trial start Phase 2: A Double-Blind, Placebo-Controlled, Dose Exploration Study of CTI-1601 in Adult Subjects With Friedreich's Ataxia source ↗
Trial start —: Determine Range of Tissue Frataxin Concentrations and Other Potential Biomarkers source ↗
Trial start Phase 1: Multiple Ascending Dose Study of CTI-1601 Versus Placebo in Subjects With Friedreich's Ataxia source ↗
Trial start —: A Study to Assess Variation in Potential Biomarkers in Friedreich Ataxia source ↗
Trial start Phase 1: Single Ascending Dose Study of CTI-1601 Versus Placebo in Subjects With Friedreich's Ataxia source ↗
Upcoming milestones
2027-01 (ESTIMATED) · Phase 2 · An Open-Label Study of CTI-1601 in Subjects With Friedreich's Ataxia · NCT06447025
2029-07 (ESTIMATED) · Phase 3 · A Study to Evaluate the Efficacy and Safety of Subcutaneous Nomlabofusp in Subjects With Friedreich's Ataxia · NCT07778836
Estimated primary completion per ClinicalTrials.gov. Dates move.
Funding
Raised: $169.0M. Last 2 years.
Follow-on offering: $100M (total, as published), announced Feb 26, 2026. Source: company release on GlobeNewswire. source ↗
Follow-on offering: $69M (total, as published), announced Jul 31, 2025. Source: company release on GlobeNewswire. source ↗
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