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A Safety and Efficacy Study Evaluating CTX112 in Subjects With Relapsed or Refractory B-Cell Malignancies
Sponsor: CRISPR Therapeutics AG
Summary
This is an open-label, multicenter, Phase 1/2 study evaluating the safety and efficacy of CTX112™ in subjects with relapsed or refractory B-cell malignancies.
Official title: A Phase 1/2, Open-Label, Multicenter, Dose Escalation and Cohort Expansion Study of the Safety and Efficacy of Anti-CD19 Allogeneic CRISPR-Cas9-Engineered T Cells (CTX112) in Subjects With Relapsed or Refractory B Cell Malignancies
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
120
Start Date
2023-03-10
Completion Date
2030-02
Last Updated
2025-11-14
Healthy Volunteers
No
Conditions
Interventions
CTX112
CTX112 (CD19-directed T-cell immunotherapy comprised of allogeneic T cells genetically modified ex vivo using CRISPR-Cas9 gene editing components)
Locations (7)
University of Kansas
Westwood, Kansas, United States
Washington University
St Louis, Missouri, United States
SCRI
San Antonio, Texas, United States
University of Utah
Salt Lake City, Utah, United States
Royal Prince Alfred
Camperdown, New South Wales, Australia
Alfred Health
Melbourne, Victoria, Australia
Sir Charles Gairdner Hospital
Nedlands, Western Australia, Australia