RecruitingPhase 1NCT06925542

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

Studying Diffuse cutaneous systemic sclerosis

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Key facts

Sponsor
CRISPR Therapeutics
Intervention
CTX112(biological)
Enrollment
80 enrolled
Eligibility
18-70 years · All sexes
Timeline
20252031

Study locations (8)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06925542 on ClinicalTrials.gov

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