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RECRUITING
NCT05643742
PHASE1/PHASE2

A Safety and Efficacy Study Evaluating CTX112 in Subjects With Relapsed or Refractory B-Cell Malignancies

Sponsor: CRISPR Therapeutics AG

View on ClinicalTrials.gov

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

Interventions

BIOLOGICAL

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