NCT07549698

Safety and Preliminary Efficacy of CTX112 in Adult Participants With Relapsed/Refractory Hematologic Autoimmune Disease

Recruiting
PHASE1Ages 18+InterventionalTreatment
CRISPR Therapeutics AG
~60 participants
Updated 2026-07-22 on ClinicalTrials.gov
What's tested:CTX112

At a glance

Recruiting sites
6 of 10 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
To evaluate the safety of CTX112 in adult participants with refractory hematologic autoimmune diseases, including ITP or wAIHA.
Measured over From CTX112 infusion up to 28 days post infusion.
Warm Autoimmune Hemolytic Anemia (WAIHA)
ITP - Immune Thrombocytopenia
Warm Autoimmune Hemolytic Anemia
Immune Thrombocytopenic Purpura
10 sites across 4 states
Germany4
Spain4
Minnesota1
Nebraska1

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  • To evaluate the safety of CTX112 in adult participants with refractory hematologic autoimmune diseases, including ITP or wAIHA.From CTX112 infusion up to 28 days post infusion.

    Incidence of dose-limiting toxicities.