drugset / Trial / NCT06925542

A Safety and Efficacy Study Evaluating CTX112 in Adult Subjects With Refractory Autoimmune Disease

NCT06925542 ↗

Phase 1 Recruiting 80 enrolled CRISPR Therapeutics AG
NaSequentialOpen-labelTreatment

Summary

This is a single-arm, open-label, multicenter, ascending dose Phase 1 study evaluating the safety and preliminary efficacy of CTX112 in adult subjects with refractory autoimmune diseases, including active systemic lupus erythematosus (SLE), systemic sclerosis (SSc), or idiopathic inflammatory myopathy (IIM).

Timeline

Start
2025-03-10
Primary completion
2031-12-31
Completion
2031-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject CTX112 Cell therapy — Intravenous