CRISPR Therapeutics registers Phase 1/2 trial of CTX112 in neurologic autoimmune disease
New study will test the allogeneic CAR-T therapy across five B-cell-driven neurological autoimmune conditions, not yet recruiting.
CRISPR Therapeutics registered one new trial this week.
- The Phase 1/2 trial (NCT07804004, sponsor study ID CRSP-AID-502) is listed as not yet recruiting, with an estimated start date of 2026-11-01 and estimated primary completion of 2029-12-30.1 The trial may enroll up to 220 participants.1 It will evaluate CTX112, also called Zugocabtagene geleucel or zugo-cel, a CD19-directed allogeneic CAR-T cell therapy made using CRISPR-Cas9 gene editing, in adults with Progressive Multiple Sclerosis, relapsing Neuromyelitis Optica Spectrum Disorder, relapsing Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease, refractory Autoimmune Encephalitis, and refractory Stiff-Person Syndrome.1 The primary outcome is safety of CTX112 through 28 days post-infusion, including incidence of dose-limiting toxicities.1
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