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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
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT05643742-Jun 24, 2026
NCT ID
NCT05643742
Status
RECRUITING
Phase
Phase 1/2
Sponsor
CRISPR Therapeutics AG
Executive brief
Investment-Ready Snapshot
CRISPR Therapeutics AG is advancing CTX112, an allogeneic CAR T-cell therapy targeting CD19, into clinical trials for relapsed or refractory B-cell malignancies. The market for CAR T-cell therapies is expanding, particularly in hematological cancers, with significant competition from established players like Novartis and Gilead. The successful development of CTX112 could position CRISPR Therapeutics as a key player in the CAR T landscape, especially given the innovative CRISPR-Cas9 gene-editing technology employed. However, the company must navigate regulatory hurdles and demonstrate superior efficacy and safety profiles to differentiate CTX112 from existing therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05643742
Indication
B-cell Lymphoma
Modality
gene therapy
Target
CD19 (Cluster of Differentiation 19), a B-cell specific surface antigen targeted by the engineered T cells in CTX112.
Intervention
CTX112
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.